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Journal of Immunology Research
Volume 2016 (2016), Article ID 7203587, 18 pages
Review Article

Hib Vaccines: Past, Present, and Future Perspectives

1Biological Sciences Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589, Saudi Arabia
2Main Medical Laboratory, Medical Services, Saudi Airlines, P.O. Box 167, Cost Center 507, Jeddah 21231, Saudi Arabia
3Therapeutic and Protective Proteins Laboratory, Protein Research Department, Genetic Engineering and Biotechnology Research Institute, City for Scientific Research and Technology Applications, New Borg EL-Arab, Alexandria 21934, Egypt

Received 31 October 2015; Accepted 24 December 2015

Academic Editor: Clelia M. Riera

Copyright © 2016 Adi Essam Zarei et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Haemophilus influenzae type b (Hib) causes many severe diseases, including epiglottitis, pneumonia, sepsis, and meningitis. In developed countries, the annual incidence of meningitis caused by bacteria is approximately 5–10 cases per population of 100,000. The Hib conjugate vaccine is considered protective and safe. Adjuvants, molecules that can enhance and/or regulate the fundamental immunogenicity of an antigen, comprise a wide range of diverse compounds. While earlier developments of adjuvants created effective products, there is still a need to create new generations, rationally designed based on recent discoveries in immunology, mainly in innate immunity. Many factors may play a role in the immunogenicity of Hib conjugate vaccines, such as the polysaccharides and proteins carrier used in vaccine construction, as well as the method of conjugation. A Hib conjugate vaccine has been constructed via chemical synthesis of a Hib saccharide antigen. Two models of carbohydrate-protein conjugate have been established, the single ended model (terminal amination-single method) and cross-linked lattice matrix (dual amination method). Increased knowledge in the fields of immunology, molecular biology, glycobiology, glycoimmunology, and the biology of infectious microorganisms has led to a dramatic increase in vaccine efficacy.

1. Introduction

Encapsulated H. influenzae type b (Hib) causes many severe infections, including sepsis, epiglottitis, pneumonia, and meningitis. Occasionally, encapsulated nontype b strains of H. influenzae, mostly type a, are able to produce invasive infections similar to Hib infections. In contrast, nontypeable (unencapsulated) strains are rarely a source of severe infections but most frequently generate infections of mucus membrane, such as conjunctivitis, sinusitis, and otitis media [1, 2]. Hib meningitis has been common in developed countries and hence must be presented along with the other Hib systemic diseases. In 1972, it was approximated that one in 280 newborns are infected with Hib in the first 5 years of life [3]. In a number of populations, including Australian aboriginal and Alaskan Eskimo children, incidence of meningitis caused by Hib has reached 1/50 to 1/30 newborns per year [4, 5]. The Hib meningitis mortality rate is about 5 to 10%, and around 30% of cured infected children have deficits of the central nervous system (CNS) varying from seizures, to deafness, to mental retardation [6]. Furthermore, Hib antibiotics resistance is increasing; around 30% of isolated Hib is ampicillin-resistant, and Hib meningitis in children is tenfold more transmissible than Neisseria meningitidis meningitis [7, 8]. In the prevaccination era, Hib epiglottitis caused much more morbidity and mortality than Hib meningitis and was second to Hib meningitis as the most common systemic Hib infection in Sweden [9].

According to the Global Alliance for Vaccines and Immunization (GAVI), more than 1.5 million children (around three per minute) die each year from diseases that could be prevented by vaccines. Enhancements in related fields such as biotechnology, virology, synthetic biology, and genetics offer a novel array of tools to advance vaccinology [10].

Capsular polysaccharide (CPS) covers the surface of some pathogenic bacteria, such as Hib, and is accessible for detection by cells of the immune system including macrophages, B cells, and dendritic cells. Moreover, most CPSs have unique structures that differ from those of mammalian glycans; and their accessibility by the immune cells and induction of immune responses specific for CPS make them excellent vaccine candidates [11]. The structure of the replicating disaccharide units of CPS of Hib is presented in Figure 1 [12]. These units are linked through phosphor-diester bonds, which generate the acidity of the polysaccharide Hib molecule [13].

Figure 1: H. influenzae type b capsular polysaccharides repeating unit.

The immunogenicity of CPS antigens leads to their categorization as T cell independent type 2 (TI-2) immune response, which stimulate protective antibodies without help from MHC-II classified T cells. CPSs trigger activation of the complement factor C3d by the complement alternative pathway; subsequently, primed marginal-zone B cells in the spleen travel to the germinal center and connect to polysaccharide-C3d via their CD21 complement receptor [14]. However, isotype switching follows, and responses against CPSs antigens occurred not only by IgM, but also by IgG and IgA [15, 16]. A specific signaling system might manage the vital responses of these antibodies [17], which differ in character and size among individuals [18] according to their age and earlier infections [19].

The naivety of the immune systems of young children and their relative incompetence compared to those of adults render children more vulnerable to Hib infections. Moreover, the integument and mucosa delicacy, as a kind of structural naivety, may play a role in susceptibility. Many studies have compared the immune systems of infants and adults, considering the role and potency of nearly every constituent of the immune system, humoral and cellular, innate and adaptive, that may make the infant immune system vulnerable [20]. The marginal zone of the human spleen is not completely formed until one to two years of age, numbers of CD21-expressing B cells in the marginal zone and complement are small at childbirth, and CPS-specific antibodies productions are limited or absent in newborns [21, 22]. At delivery, very little IL12 is produced from antigen presenting cells (APCs), and with the exception of live attenuated vaccines, which have a maturation effect on neonatal APC, most vaccines have little capability to prime protective T-helper 1 responses in newborns [2328]. The suppression of antibody responses (mainly against protein antigens) in early life may be caused partly by transplacentally acquired IgG, which fades after birth according to a half-life of about 28 days; this transplacental IgG does not cause downregulation of T cell function [29].

When used as vaccines, CPS antigens of several infectious bacteria stimulate considerable protection by inducing antibody production [30]. Without considering herd immunity, the effectiveness of the conjugate Hib vaccine may range between a 46% and 93% reduction in invasive disease caused by Hib. The success and safety of the Hib conjugate vaccine have been confirmed in pharmacovigilance screening. Adverse reactions to the conjugate Hib vaccine are rare; only individuals with hypersensitivity to the vaccine’s constituents are subject to contraindications [31]. However, children who contract Hib disease regardless of proper immunization must be examined for suspected malfunctions in their immune system that make them sensitive to the infection [32].

Several factors may explain the low introduction level of Hib conjugate vaccines in the majority of developing countries, such as the absence of statistics that reflect the burden of disease and the troubles facing its estimation and calculation, political failure to consider Hib infection a health crisis, and the absence of practices related to vaccinology [33, 34]. The use of smaller doses of antigen and smaller quantities for vaccine injection in developing countries could support the introduction of vaccines by immunization schedules such as those routinely planned for children [35].

The use of the Hib vaccine in Saudi Arabia began in April 1998 at King Fahad National Guard Hospital, where it was used routinely for all infants in the hospital [36]. Subsequently, vaccine became obligatory in the national immunization program in 2000 and since then cases of Hib have declined considerably. During three years (2001–2003) there were 30 cases of H. Influenzae invasive disease, compared to only 6 cases in the following three years (2004–2007) [37]. According to the Saudi Ministry of Health 2013 Statistics Book, coverage of the pentavalent vaccine (which includes diphtheria, pertussis, tetanus, Hib, and hepatitis B) is 97.7% [38]. This review on the vaccinology of Hib will serve as a valuable source of information for public health officials and decision-makers.

2. Hib Vaccines

2.1. CPS Vaccines and Adjuvants

The idea of using the bacterial CPS in vaccines dates back to 1930s and involves inducing polysaccharide-specific antibodies to protect against pathogenic bacteria [3941]. The CPS of Hib, polyribosylribitol phosphate (PRP, Figure 1), has several significant characters, such as immunogenicity in humans, the same antigenic properties in all strains of type b, and stimulation of anti-Hib antibodies. In 1985 purified PRP was certified for use in a vaccine in the United States. However, rapid reduction of antibodies stimulated by purified PRP was the main drawback, as it offered no immunological memory [42]. The solution was to give more injections as boosters that took dropping levels of antibodies back up to postvaccination levels, but this failed to generate either strong response nor immunological memory, as injection of the booster did not stimulate IgM class switching to IgG [43]. In Finland, the vaccine was very successful in experiments in children 18 months and older, while in the United States postmarketing surveillance showed fluctuating efficiency (from 69% to 88%) [44]. However, the level of ≥0.15 μg/mL of anti-PRP in unvaccinated children and level of ≥1.0 μg/mL in vaccinated children were considered protective against Hib infections, as suggested by many studies [45].

CPS-specific receptors on the surfaces of native B cells (BCRs) recognize the multivalency and large size of CPSs. Upon immunization with pure CPS, these BCRs bind to the CPSs and the BCR-CPS complex stimulates the B cell to induce and secrete IgM antibodies against CPS. In the event of bacterial infection following CPS immunization, IgM antibodies bind to the CPS expressed on the surface of the particular pathogenic bacteria and help eradicate that pathogen [11, 46].

The compounds that are able to enhance and/or regulate the antigen’s immunogenicity are called adjuvants and represent a varied collection of compounds. Put simply, an adjuvant is a vaccine assistant (adjuvare is a Latin word meaning “to help”) and is a synonym of immunostimulant. It can be a combination of one or more compounds that act and function differently: that is, a molecule, carrier or depot, immunomodulator, and/or immunostimulant. The adjuvant industry has grown to meet demand for enhancing the immunogenicity of insufficient vaccines. The two main basic mechanisms by which adjuvants act are enhancing antigen presentation to the immune elements and stimulating immunity so that a stronger or wider response is reached. By these means, immunogenicity can be improved and/or doses of the vaccines can be decreased to a level that has no negative effect on immunogenicity [47, 48].

Animals, plants, and bacteria are sources of widespread immunostimulatory constituents of several adjuvants that function as stimulators of immunological components. One highly effective method of adjuvanticity is the conjugation of inactivated toxoids to purified PRP. This method has been used successfully in anti-Hib, anti-N. meningitidis, and anti-Streptococcus pneumoniae conjugate vaccines. Compounds such as alum and calcium phosphate are the only mineral salts authorized for use as adjuvants with vaccines in the United States since the 1920s. The primary mineral salt adjuvant for use in humans is alum, either as aluminum hydroxide or as aluminum phosphate. It acts by creating a depot spot, such that mild and constant release of the antigen improves presentation to immunological components [47, 48].

Studies have investigated the role of innate cells in adjusting adaptive immunity. Numerous antigen presenting cell (APC) signals are needed to start T-helper responses. First, a signal is activated by presentation of a certain peptide by class II molecules to the T cell receptor (TCR). Without the contribution of an additional signal, abortive and anergy responses are stimulated; a costimulatory second signal is required, via receptor-ligand contacts among APC/T antigens. It appears that another (preceding) signal, the zero signal, is required to stimulate APCs and orient subsequent Th responses, for example, throughout IL12 for Th1 responses. Zero signals are typically stimulated by detection of pathogen-associated molecular patterns (PAMPs) through pathogen recognition receptors (PRR), involving toll-like receptors (TLRs). APCs class I presentation for CD8 stimulation may be controlled by these signals. Promotion of CD4 cells that secrete interferon gamma (IFNg) by Th1 adjuvants is not enough to activate CD8 cytotoxic T cells, which also need class I antigen presentation [48]. These outcomes closely connect native immunity and the following adaptive immunity. The essential signals and steps needed to stimulate T and B cell responses suggest that signals of innate immunity also control the quality (not only the degree) of adaptive immunity. For example, innate cells permit adaptive T and B cells to differentiate and grow, and Th1 polarization is observed throughout IL12 secretion [48]. Adjuvants may be able to perform on any of these signals. Affecting exactly costimulatory molecules (second signal) throughout antibodies, chemokines, or cytokines is an attractive option [49], but it may lead to unfocused overreaction status [48].

While earlier development of adjuvants generated effective products, there is still a need to create new generations, rationally designed based on recent discoveries in immunology, especially innate immunity. The safe and optimal preparation of adjuvants is the most challenging task in the field. Little work has been dedicated to adjuvants with free PRP or with glycoconjugate vaccines, compared to protein vaccines. However, a number of researchers have examined the capacity of several molecules, especially TLR agonists, to increase the immunogenicity of conjugated or free carbohydrate antigens [48]. Free PRP vaccines against Hib are no longer used in the United States [50].

2.2. Conjugate Vaccines and Adjuvants

Most proteins need participation of T cells to stimulate antibody synthesis and consequently are considered T cell dependent (TD) antigens [51]. These proteins promote increased response of antibodies in the booster vaccine and encourage class switching from IgM to IgG via the involvement of T-helper cells in the immune process. Moreover, subsets of B-memory cells are generated from B cells in TD immunity, resulting in the establishment of memory against a specific antigen. This is accomplished by covalently connecting PRP to protein carriers, which results in production of Hib glycoconjugate vaccines [52]. By this kind of conjugation, the humoral immune response is induced with features of TD immunity reactions, such as affinity maturation, memory, and, crucially, the presence of immunogenicity in children aged more than 2 months [30]. Development of protein-conjugated polysaccharide vaccines has been accelerated by increasing antibiotic resistance and the need to stop Hib infections in high-risk populations [12].

In 1931, Avery and Goebel invented the improvement of polysaccharide immunogenicity by the tool of conjugation to proteins. Nevertheless, this was not widely practiced until the invention of polysaccharide conjugate vaccines. In the 1970s through 1980s, the application of bacterial polysaccharides and proteins for stimulating immunity increased. Conjugate Hib vaccines are created by Hib CPS (polyribosylribitol phosphate; 5-D-ribitol-(11)-β-D-ribose-3-phosphate; PRP) attached to proteins, with excellent safety and distinctly different structures and conformations [5355]. The first invented and approved conjugate vaccine in the United States was created from PRP conjugated to diphtheria toxoid (PRP-D), which was withdrawn from the market soon after introduction of more effective vaccines using meningococcal outer membrane protein (PRP-OMP), CRM197 (PRP-CRM) protein carriers, or tetanus toxoid (PRP-T) [56].

The structure of polysaccharides and carrier proteins properties largely determine the immunogenicity of the conjugates, and the techniques used in the conjugation process can play a central effect. The conjugation process should be uncomplicated and mild and cause little alteration to the constituents, such that it does not damage important epitopes on either the protein or the PS, cause undesired depolymerization of the PS, or introduce any harmful epitopes. While a number of conjugation chemistries are available for the synthesis of PS-protein conjugates [57], only a few have been used in licensed vaccines. For proteins, surface-exposed amines (e.g., amines of lysine residues) and carboxyls (e.g., the side chains of carboxyl of aspartic and glutamic acid residues) are the major groups used for conjugation [58, 59]. Prior to the conjugation process, fermentation/isolation techniques of Hib CPS are used to produce Hib conjugate vaccines on a large scale [60].

Chemical synthesis of the Hib saccharide antigen was a breakthrough in conjugated vaccines, which led to development of a novel type of Hib conjugate vaccine. This generally includes the formulation of the oligosaccharide moiety by chemical or enzymatic methods, which represents the immunological specificity for the vaccine and then attachment of this to an immunogenic protein by a linker. Chemical synthesis of these complex oligosaccharides is difficult and requires a suitable mixture of techniques that allow appropriate treatments by applicable glycosyl donors, acceptors, protecting groups, and coupling reactions settings. This option has come to be accessible due to notable growth of enzymatic and chemical oligosaccharides preparation [6164]. Currently, the synthetic Quimi-Hib vaccine is approved for use in the National Immunization Program in Cuba [64]. Figure 2 summarizes the types of currently used Hib vaccines according to the type of PRP.

Figure 2: Schematic diagram summarizing the types of currently used Hib vaccines according to the type of PRP (nPRP-native PRP, oPRP-oligosaccharide PRP, and sPRP-synthetic PRP).

Glycoconjugate syntheses include the usage of well-defined or random activation sites in the polysaccharide as possible attachment sites for proteins. The choice of method for activation is mainly governed by the molecular size of the polysaccharide. Large polysaccharides are frequently arbitrarily activated, while selective activation at the reducing end is typical for oligosaccharides [12]. Molecular differences between conjugation methods do not affect their clinical performance but do influence strategies for quality control [57].

The conjugation process can be divided into the following steps (Figure 3): (I) preparing the carbohydrate, (II) preparing the protein carrier, (III) performing the conjugation, and (IV) finishing. Some conjugation schemes combine several steps, whereas in others a particular step may be unnecessary [58].

Figure 3: Main steps in the glycoconjugate process.

Preparation of the Carbohydrate(1)Sizing. Native CPSs have molecular sizes in the millions of Daltons, and solutions tend to be viscous. Reducing the molecular size of the PSs decreases their viscosity and makes the solutions easier to handle.(2)Activation. Carbohydrates have hydroxyl groups, which are relatively inactive and must be translated into a more reactive form (functional group). The activated PS can be either immediately conjugated to the protein or further functionalized. The positions of the activated groups determine the positions of the linkages on the PS.(3)Functionalization. This procedure adds reactive chemical groups to the carbohydrate or converts the activated PS into a more stable form while maintaining its reactivity. Functionalization can include the addition of a spacer molecule between the carbohydrate and the reactive group and in some cases is a multistep process [58].

Protein Carrier Preparation. Amines (the amines of lysines) and carboxyls (glutamic and aspartic acids) can be applied to link directly to the activated or functionalized carbohydrate. However, some protocols rely on the addition of chemical groups that are more reactive and/or more specific in their reaction with the activated or functionalized carbohydrate than carboxyls or amines. Functionalization of the protein can also provide a spacer molecule such that the reactive groups on the protein are more accessible to the carbohydrate [58].

Conjugation. Conditions that promote conjugation-high concentrations of protein and PS and high numbers of reactive groups bring the risk of excessive cross-linking when both the protein and the PS have multiple reactive groups. Also of concern is the need to confirm uniform mixing and reaction, which can be challenging on a production scale due to the high viscosity of the PSs. Careful control over factors relevant to the particular chemistry is crucial for successful conjugation. These factors include pH, temperature, the ratio of protein to PS, and the concentration of each. The type of linkage achieved depends on the chemistry and may be reversible or irreversible [58].

Finishing(1)Quenching. Quenching inactivates any residual groups to prevent further cross-linking. This step is commonly completed with monovalent blocking reagents, such as ethanolamine or glycine.(2)Locking. A locking (or blocking) step makes the conjugation linkage fundamentally irreversible.(3)Purification. The conjugate must be purified to eliminate the conjugation reagents and to guarantee low levels of unconjugated carbohydrate and protein. Unconjugated PS has been shown to decrease the immune response to the conjugate [65, 66].

Two models for carbohydrate-protein conjugation have been established: the single ended model (terminal amination-single method) and cross-linked lattice matrix (dual amination method) [12, 57].

2.2.1. Terminal Amination-Single Method

This method imitates the structural features of glycoproteins by which protein is connected to the oligosaccharides across its reducing end, resulting in the single ended model (Figure 4) [57]. The model differs from native glycoproteins in terms of polymeric carbohydrate chain length, connection sites, and structure. The antigenic carbohydrate positions of this model of neoglycoprotein are instantly available to antibodies. The carbohydrate hapten density is the main factor that influences the antigenicity of these neoglycoproteins [12].

Figure 4: Single ended model (neoglycoprotein).
2.2.2. Dual Amination Method

A cross-linked lattice matrix is molded by several connection points formed by conjugation of an antigenic carbohydrate and a protein carrier (Figure 5) [57]. Vaccine solubility can be enhanced by decreasing the quantity of cross-linked points on the polysaccharide chain, which shrinks the conjugate matrix and cross-linking. The large number of reachable antigenic spots on the superficial cross-linked lattice matrix guarantees the molecule’s extraordinary immunogenicity, despite the quantity of cross-linking [12].

Figure 5: Cross-linked lattice model.

The tendency of the carrier protein to denature is a limiting factor for conjugation. However, immunogenicity can be maintained if an alteration in the tertiary geometric shape is able to influence the antibody specificity. The modification of hydroxyl, carboxyl, hemiacetal, phenoxyl, amino/imino, or mercapto/disulfide functional group is thus an important step in the conjugation process. Sodium cyanoborohydrate is used in conjugation chemistry involving reductive amination to selectively reduce intermediate imine adducts known as Schiff bases [67, 68]. This reduction pushes the system to equilibrium, affording stable adducts, despite the formation of Schiff bases being a disfavored equilibrium technique in water. Glycosylamine formation is straightforward reaction whereby carbohydrates are treated with saturated solution of ammonium bicarbonate for 5–7 days at room temperature. Catching the glycosyl amine by creation of the peptide with iodoacetic acid and reaction of the cysteine residue of the protein to the thiol reactive iodoacyl group produces neoglycoconjugates [6971]. The spacer arm, an allyl group presented at the reducing end, may be employed to make aldehyde by ozonolysis and can be joined to the protein amine groups by reductive amination.

A thiol reactive maleimide group can be connected to a carbohydrate over a spacer arm to increase the availability of functional groups and reactive centers [72]. Methods using N,N′-dicyclohexylcarbodiimide (DCC), water soluble 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC), or activation of carboxylic groups by sulfo-NHS for combined amino functionality in a carbohydrate or protein have been broadly applied to the production of neoglycoproteins [73, 74]. p-Nitrophenyl glycosides may be converted to highly reactive diazonium salts to create electron-rich adducts, aromatic tyrosine, or tryptophan residues [75]. Although regarded as limited by recent measures, diazo coupling grants strong conjugates immunogenicity and has been broadly utilized for preparation of conjugate vaccines such as the type 3 S. pneumoniae CPS vaccine. By nonspecific activation of hydroxyl groups and creation of reactive cyanate esters, cyanogen bromide has been employed to conjugate carbohydrates and protein amino groups in aqueous alkaline solution via a stable O-alkyl isourea linkage [76]. When a phosphate presents at the terminal end, it frequently appears in an internal ester, because of the closeness of the adjoining hydroxyl group on the ribitol moiety to the phosphate hydroxyl; this internal esterification triggers Hib PS hydrolytic lability at both alkaline and acid pH and at elevated temperature [77].

Adjuvants for conjugate vaccines include salts of aluminum. Depending on the conjugate, the adjuvant may be unimportant or crucial [78]; or it may have a harmful influence on the stability of the conjugate, as with Hib conjugates vaccines [79]. Toll-like receptor 9 (TLR9) agonists have also been employed as adjuvants, helping to compensate for immunodeficiency such as that faced in late or early life [8082]. Immune interference arising in polyvalent conjugate vaccines could be lessened by adjuvants via suppression of the B or T cell dependent carrier, among other methods [8385].

Quality control of Hib conjugate vaccines by laboratories, manufacturers, and the government depends on physicochemical procedures for screening of production consistency and recognition of any defects in batches over time. Biological tests are performed by manufacturers only during vaccine production to confirm stimulation of TD immunity by conjugate vaccines and to guarantee their safety [86].

Since 1997, the World Health Organization (WHO) has recommended the Hib conjugate vaccine for national immunization programs anywhere resources exist and disease burden data support its priority [39, 8789]. Before 1997, however, only a minority of children in developing countries had access to the Hib conjugate vaccine, due to shortages arising from sparse statistics on disease burden [90], lack of belief in the vaccination value, lack of awareness, and greater priority of other concerns [91]. The vaccine was supplied by only one manufacturer to the United Nations International Children’s Emergency Fund (UNICEF) [92], and its three-dose course was much more expensive than the combined price of all other vaccines in the standard immunization for infants specified by the WHO Expanded Program on Immunization (EPI). The estimated price of the Hib conjugate vaccine was twofold higher than the measles, mumps, and rubella multivalent vaccine, and it was more costly than conventional vaccines in EPI (3.15 versus US$1.4/dose) [93]. Because of a lack of competition, the vaccine price remained high for several years [92]. The vaccine formulation choice (monovalent or multivalent) (Table 1) and final product vialing (1- or 10-dose vial) were crucial factors in the introduction of the Hib vaccine in North and South America. These two factors affect the vaccine wastage level, cost, reconstitution necessity, space of cold chain, and education events for medical employees [94, 95].

Table 1: Summary of the most important Hib vaccines in U.S. Food and Drug Administration (FDA) and The European Medicines Agency (EMA) up to 20 December 2015.

The regimen of three doses in the first year of life, with a fourth dose given in the second year, is followed in majority of the world. A three-dose regimen without the fourth dose is typical in low-income countries. Generally the Hib conjugate vaccine is given as a one-injection polyvalent together with tetanus toxoid, diphtheria toxoid, and whole-cell or acellular pertussis (DTwP or DTaP), and sometimes additionally with hepatitis B antigen (Table 1) and/or inactivated poliovirus [47].

In the 1990s patent law prevented vaccine manufacturers in developing countries from acquiring the techniques for making Hib conjugates [96, 97]; and markets were cautious due to a lack of dependable estimation. Additionally, manufacturers in developed countries began cancelling conventional manufacture of DTwP vaccines, which were less costly and hence obtainable to UNICEF for developing countries [98]. To deal with these obstacles, the National Institute for Public Health and the Environment/Netherlands Vaccine Institute (RIVM/NVI, Bilthoven, Netherlands) initiated a plan in 1998 to develop commercially viable and scalable Hib conjugate vaccine production, without patent violation, by employing technology transmissible to manufacturers in developing countries. Further assistance for the growth of combined vaccines containing the Hib conjugate indicated that manufacturers, by acquisition of entrance to technology for the Hib conjugate vaccine, could subsequently confirm a sustainable supply of inexpensive and valuable vaccines [98].

Founded in 2000, the Developing Countries Vaccine Manufactures Network (DCVMN) was formed to distribute surveillance against identified and emergent contagious infections, with the goal of raising the obtainability and quality of vaccines inexpensive to everyone. DCVMN is an international alliance of manufacturers that provides data and professional education plans, development of technology, inspiring transfer of technologies, advanced research and development, and community teaching regarding the accessibility of secure, cheap, and effective vaccines. The network grew to involve 44 manufacturers in 16 territories and countries, creating and distributing >40 several vaccine types [99]. Arabio, founded in 2005, was the first biopharmaceutical company in the Gulf Cooperation Council (GCC), located in Jeddah BioCity with Vacsera as a limited liability company, and is a member of DCVMN. Arabio focuses on plasma, biopharmaceutical, and vaccine products. The range of developments planned by Arabio could establish it as the leading biological company of its category in the Middle East [100].

3. Future Perspectives

The immune and central nervous systems are characterized by their ability to retain memory. This exceptional quality creates many opportunities for health interventions, such as prophylactic immunization. Advances in molecular chemistry and biology, glycobiology, glycoimmunology, pathogen biology, and immunology have led to substantial increases in vaccine efficacy. Current vaccines are commonly made from highly purified antigens or hapten obtained from or designed on the most immunogenic parts of pathogens. The latest molecular biology advances also promote techniques helping in immune system stimulation [12]. Figure 6 summarizes the most important fields in the future of vaccinology as whole and Hib vaccines in particular. In addition, new vaccinology concentrates on tools that offer sustained immunogenicity with better safety. These technologies consist of employing engineered antigens, subunits from pathogens (polysaccharides or proteins), or vectored antigens. The vector is a harmless virus or bacterium in which a gene can be enclosed and expressed. This technique has come to dominate the field due to its usefulness for hard-to-reach pathogens, such as intracellular pathogens [101].

Figure 6: The most important fields in the future of vaccinology as a whole and Hib vaccines in particular.

Vaccinology is further improving via development of more adjuvants, combination vaccines, and new methods of administration. New administration methods include transcutaneous (intradermal) immunization (TCI), which has potential for use in humans, whereby antigens are transported by Langerhans antigen presenting cells to nearby lymph nodes, directly stimulating systemic immunity. A major model for this method is the intradermal influenza vaccine, which penetrates the epidermis with a microneedle and creates the same immune responses as intramuscular vaccines [101, 102]. Moreover, via an ADP-ribosylating exotoxin in mouse, such as the heat-labile enterotoxin of Escherichia coli or its mutants (LTK63 and LTR72) or cholera toxin, TCI activates antitoxin protecting responses and the coadministered antigen [103108].

Combination vaccines are increasingly significant for efforts to improve vaccination acceptance by the public, as they reduce the number of injections essential for complete immunization (Table 1). Combined vaccines help to achieve high vaccination coverage and well-timed vaccination by minimizing occurrences of delay. Including novel antigens on current high-coverage vaccines is an effective method for presenting novel antigens to schedules of vaccination [109]. Studies conducted in Germany [110] and the United States [39, 111] confirm that combined vaccines can lead to improved coverage of specific antigens, and with further well-timed vaccination, a greater proportion of children can obtain all recommended vaccines at the appropriate age [112].

In Germany, 5-year surveillance was conducted to inspect the efficiency of hexavalent vaccines and found that DTPa-HBV-IPV/Hib was 90.4% effective for a complete three-dose primary series and 100% for a complete primary series with a booster (regardless of the priming Hib vaccine) [113]. Long-standing effectiveness of a combined Hib-DTPa-based vaccine on a 3-, 5-, and 11-month schedule has also been confirmed in Sweden, as incidence in children younger than 4 years was approximately 0.4/100,000 in between 2005 and 2008 [114].

Maternal immunization to protect from pathogenic organisms has been suggested as a technique to protect newborns, as maternofetal immunoglobulin transfer occurs through the placenta and maternal immunoglobulins appear in the fetus blood. Maternal immunization with Hib polysaccharide and conjugate vaccines appears to be a successful approach for delivering antibodies protective levels to infants. Maternal immunization studies [115, 116] have recognized several factors affecting the placental passage of immunoglobulins. Compared to IgM and IgA antibodies, IgG antibodies more effectively cross the placenta, and antibodies in the IgGl subclass are better for transport than those in the IgG2 subclass [117]. Antibody placental crossing is moreover subject to the vaccination time through pregnancy [116]. The detection of factors affecting antibody placental crossing may be fundamental to choosing plans for future maternal immunization [118].

Synthetic oligodeoxynucleotides enclosing cytosine triphosphate deoxynucleotide-phospho-diester-guanine triphosphate deoxynucleotide (CpG) immunostimulatory sequences (ISS) may function as danger signals of bacterial attacks and trigger immune warfare [119, 120]. While the exact mechanism of action is not fully understood, it is thought that ISS act as PAMPs able to connect PRR, mainly expressed on the surface of antigen nonspecific innate immune cells [121]. The presence of APC-expressed PRR by PAMPs activates innate cells that gain the power to stimulate adaptive immunity cells, which in turn support the launch of an antigen-specific immune action. ISS are made in accordance with DNA sequences of bacteria that may stimulate innate immunity cells [122]. ISS stimulate innate immunity in the same way as bacterial infections, therefore supporting the specific immunity to the antigen, in contrast to other adjuvants, such as mineral oils or alum, whose immunostimulatory action extends delivery of antigens [120]. The danger signals produced by ISS provide a powerful adjuvant to stimulate the anti-conjugated PS type one immunity response.

The adjuvant effect of ISS effectively improves the anti-carrier immunity response. Anti-diphtheria toxoid (anti-DT) and anti-tetanus toxoid (anti-TT) antibody titers were greatly improved by ISS in the Hib-CRM and Hib-TT vaccines. Moreover, the pattern of the anti-carrier IgG subclass was affected by ISS, as IgG2a and IgG2b increased in the presence of ISS. A considerable rise in IgG3 was distinguished only in the anti-TT immune response. IgG3 is the major IgG subclass in several humoral immunity responses in the mouse that are stimulated by polysaccharide antigens but is a minor constituent of the anti-protein immune response [123]. Therefore, TT but not CRM stimulates IgG3 production in the similar cytokine milieu resulting from ISS, supporting the suggestion that the antigen structure is included in the immunoglobulin isotype switch of B-lymphocyte differentiation [124].

H. influenzae outer membrane proteins have received attention due to their antigenic excellence as potential vaccine candidates [125]. However, one significant criterion that must be met for a Hib outer membrane protein to be an effective vaccine is that the protein must have surface-exposed and antibody-accessible antigenic determinants that are common to most strains of the pathogen. At least three Hib outer membrane proteins appear to fulfill this requirement. Data on the P6 protein show that this protein has at least one surface epitope that is common to all strains [126]. To date, P2 and P6 are the best candidates for anti-nontypeable H. influenza vaccines [127]. Another method in vaccine development inserts surface-exposed proteins in outer membrane vesicles (OMV), which, in clinical trials, stimulates responses of serum bactericidal antibodies and gives rise to antimeningococcal activity [128].

3.1. Conjugation Development

The classic antigen presentation hypothesis for glycoconjugate vaccines suggests that helper CD4+ T cells identify a peptide originated from the carrier protein [129]. According to the traditional pattern, the glycoconjugate binds to the surface of a B cell whose specific job is to make antibodies to the polysaccharide component. The B cell deals with the protein portion of the glycoconjugate and exhibits a peptide from the covalently linked carrier protein in the setting of the major histocompatibility complex class II (MHC II) to the αβ-TCR of CD4+ T-helper cells. Stimulation of T cells by peptide-MHC II complexes and other costimulatory molecules leads to production of the cytokine interleukin 4 (IL-4) by the T cell, which in sequence encourages cognate B cell maturation and subsequent creation of carbohydrate-specific antibodies, with associated class switching of immunoglobulin to IgG and memory responses. This hypothesis was originally based on the theory that only protein antigens can be presented to and identified by T cells. Initial research on hapten-carrier conjugates (i.e., small molecular weight noncarbohydrate molecules connected to carrier proteins) suggested that peptide presentation is the triggering tool for glycoconjugate induced T cell activation [130].

A new study [129] strongly suggests that carbohydrate-recognizing T cells, not peptide-recognizing T cells, are the principal T cell population driving the T cell-mediated adaptive immune response. It shows that carbohydrates, which were previously thought to be “T cell-independent” antigens, can be precisely distinguished by T cells, as they are conjugated with carrier peptides that permit their presentation by MHC II molecules on the surface of APCs. These conclusions are different from the classical understanding that T cells can only recognize peptides [129]. A model new-generation glycoconjugate vaccine [129] has enriched carbohydrate T cell epitopes compared to a glycoconjugate vaccine made by traditional conjugation methods. This model vaccine is 50–100 times more immunogenic than classical vaccines. This type of carbohydrate-recognition T cell may lead to significantly better vaccines against infectious diseases. Elucidation of the T cell epitopes of glycoconjugate vaccines would allow us to imitate those epitopes and enhance vaccines by joining carbohydrate epitopes at a frequency and density that enhances immunogenicity and protection through APCs proficient processing and presentation and highly specific T cell recognition [131]. The zwitterionic polysaccharides are a class of complex carbohydrates that activate T cells [131, 132]. Figure 7 summarizes the most important approaches to the improvement of glycoconjugate vaccines.

Figure 7: The most important approaches to improve glycoconjugate vaccines.

The conjugation of biomolecules to metal nanoclusters and nanoemulsions has opened new opportunities in the design and synthesis of multifunctional and multimodal built systems for biomedical uses. Gold nanoparticles have been widely studied for their low toxicity, relative inertness, easy handling, and easy chemistry of surface control. The surface of gold can be shaped in a controlled way with various ligands through thiol chemistry, producing multifunctional and multivalent nanoparticles [101, 133].

Carrier proteins are fundamental components of classical conjugate vaccines. Peptides offer covalently bound carbohydrate epitopes to the TCR of CD4+ T cells [134]. Thus, optimization of the MHC II-binding peptide concentration in a conjugate vaccine would theoretically enhance the immunogenicity of the conjugate vaccine by increasing the number of carbohydrates that can be presented on MHC II proteins. The best approach to accomplish this is to connect polysaccharides to MHC II-binding peptides in place of the intact proteins. This would allow the presentation of significantly greater amounts of peptide-bound carbohydrate epitopes to T cells, compared to when intact proteins are. In fact, many studies have shown that conjugating peptides to polysaccharides creates highly effective conjugate vaccines [134137]. In one study, three polypeptides consisting of strings of 6, 10, or 19 human MHC II-binding peptides from several antigenic proteins were created [138]. In each construct, the MHC II-binding peptides were separated by the lysine-glycine spacer to give flexibility to the polypeptide and to permit the conjugation of the glycan to the amino side chains of the lysine spacer. The 19-valent polypeptide was then conjugated with CPSs of N. meningitides serogroups A, C, W-135, and Y [139]. In immunization tests, the polypeptide-containing glycoconjugate vaccines had greater immunogenicity than glycoconjugates that contained CRM197 as carrier protein. Compared to CRM197-based conjugates, smaller quantities of polypeptide-based conjugates stimulated a higher bactericidal antibody titer against all four meningococcal polysaccharides. This strategy illustrates the use of MHC II-binding polypeptides as carrier molecules to create greatly effective glycoconjugate vaccines. The main improvement enabled by this strategy is that these synthetic polypeptide carriers can be identified by most of the human MHCII haplotypes. Furthermore, peptide carriers can be expressed in E. coli, which makes them easy to produce for production of glycoconjugate vaccines [11].

An important step in conjugation chemistry is to improve conjugation efficiencies to levels at which residual unconjugated components, particularly free PSs, do not affect the stimulation of protective immune responses. The use of an effective, mild conjugation chemistry would allow for higher yields of vaccine. For example, reaching more than 90% efficiency of coupling of the PS may allow for a simplified purification process. It would also be needed for development of conjugate vaccines that do not require refrigeration [58].

Current improvements in carbohydrate synthesis must simplify the enzymatic and chemical preparation of well-characterized and well-defined homogenous carbohydrate antigens for further development of glycoconjugate vaccines. Several carbohydrate antigens analogs that are stable metabolically, such as S-glycosides and C-glycosides, may enhance the immunogenicity and antigenicity of the glycoconjugate vaccines. Moreover, such analogs should expand our knowledge of antibody carbohydrate identification, processing and presentation of antigens, and immune system stimulation. Such improved knowledge of glycoimmunology would facilitate the creation of the ideal glycoconjugate vaccine for a particular disease or infection. Synthetic C-glycoside analogs of tumor-combined antigens, which are metabolically stable, nonhydrolysable carbohydrates, would similarly enhance batch-to-batch consistency in vaccine manufacturing and bypass the cold storage that is generally needed to preserve and guarantee effectiveness of existing carbohydrate-based vaccines [12].

Recently, a study reported highly immunogenic PRP-TT conjugates generated from shorter chain PRP, compared to both their high-molecular-weight counterparts from the same laboratory and licensed vaccines. The authors have optimized methods to prepare more immunogenic low-molecular-weight PRP-TT conjugates in a reproducible manner. The higher reactivity of hydrazide groups compared to the lysine -amino group resulted in a shorter conjugation time and an optimal yield. The conjugates thus created are immunogenic in rats. A hallmark of this study is the development of highly immunogenic PRP-TT conjugates using short-chain PRP, which forms the basis for further development of oligosaccharide conjugates as successful vaccine candidates alone or in combination [140].

3.2. Conjugation through DNA Biotechnology

Generally, chemical approaches that allow for well-controlled conjugation reactions between distinct-length glycans and proteins [141143] are vital for designing highly immunogenic vaccines. To date, the most effective vaccines used for protection from invasive pathogenic bacterial infection are the glycoconjugate vaccines, mainly consisting of bacterial capsular polysaccharides coupling to a desired protein carrier. Within the pathogenic bacterial strains there is effective single CPS component and/or multiple CPS from different strains. The later condition makes glycoconjugate vaccine production a very hard process, since each strain requires extraction, hydrolysis, chemical activation, and conjugation to a carrier protein. To avoid this hard situation for conserved and/or nonconserved CPS of different bacterial pathogen, the use of bioglycoconjugates machinery of innovative E. coli will substantially simplify the production of glycoconjugate vaccines.

DNA biotechnology has revolutionized vaccinology and generated new methods for vaccine discovery, such as antigenome technology, reverse vaccinology, surfome analysis, genetics vaccinology, and immunoproteomics to uncover innovative immunogenic antigens [144]. Genetically engineered vaccines are expected to be a major type of future vaccines due to their high safety level, improved immunogenicity, and decreased reactogenicity. However, absence of posttranslational modifications (PTMs) machinery in E. coli limits its use for the production of recombinant biopharmaceuticals and/or biosimilars [145152]. Various posttranslational modifications including glycosylation and phosphorylation, which are critical for functional activity, do not take place in E. coli [149153]. Protein glycan coupling technology (PGCT) is a strategy that has been used to move toward the target of making structurally defined, homogenous glycoconjugate vaccines with a well-controlled conjugation reaction [154156]. N-linked glycosylation of proteins is one of the most important posttranslational modifications in eukaryotes. Kowarik et al. identified a novel N-linked glycosylation pathway in the bacterium Campylobacter jejuni and also showed the successful transfer of functionally active N-glycosylation pathway into E. coli [157]. PGCT uses the bacterial glycosyltransferase enzyme Pg1B, an oligotransferase expressed in Campylobacter jejuni, to enzymatically link a bacterial polysaccharide with a carrier protein. Pg1B specifically recognizes a 2-acetamido-containing a reducing end sugar and glycosidically links it to a carrier protein that has a specific sequence identified by the Pg1B enzyme for N-linked glycosidation. The enzymatic conjugation, and glycan and protein biosynthesis, occurs in an E. coli host strain. The target glycan, protein, and Pg1B are cloned and expressed in E. coli. This technology removes the necessity for multistep production and purification of the glycan and protein and several steps of chemical conjugation. Consequently, the process of creating glycoconjugate vaccines is shortened and vaccine production is enhanced. Furthermore, current chemical conjugation strategies require alteration of the polysaccharides or proteins (e.g., random oxidation of the sugar chain), which may change the natural epitopes and lead to generation of less-effective conjugates. Additionally, enzymatic conjugation uses highly specific substrates with distinct binding domains, and as a result, the conjugation outcomes are homogenous and structurally defined. Finally, PGCT avoids the need for pathogenic bacteria from which polysaccharides and/or proteins are isolated, as both glycan and protein synthesis and glycoconjugate assembly take place completely in an E. coli system [156].

Although the bacterial N-glycan structure is not similar to that seen in eukaryotes, engineering of glycosylation pathway of C. jejuni into E. coli has not paved the way for expressing and production of glycosylated protein E. coli [158, 159], but the glycoconjugate vaccines too [154, 156, 160164], which will avoid the chemical conjugation vaccines producers for the harsh capsular polysaccharide-protein conjugation chemical reactions. The coming challenge for synthesis of glycosylated proteins in the engineering E. coli is the robotic machinery for secretory and extracellular N-linked glycoproteins production [165].

4. Conclusion

Heterogeneity in antibody responses between individuals and racial groups is controlled by genetic allotypes, which are still only partly understood and may be well-defined for governing T-independent and T-dependent antibody responses in certain circumstances. Moreover, as immunity weakens with age and fluctuates due to previous pathogen contact, life-cycle controlling vaccines implemented for several periods of life can make the most of defense at all ages. The recent concept of “one vaccine suits everyone” to immunize individuals is the only practical concept at the current time, but it is possible that future vaccines will be developed according to national boundaries and personalized to each individual beneficiary; this is termed “vaccinomics.” Sustainment of surveillance of colonization and isolates from diseases will be a vital part of a planned strategy for immunization in coming years.

Several populations remain vulnerable to Hib disease even with vaccination. Native American populations are up to six times more susceptible to Hib infection, and Alaskan natives and Navajo Indians still get Hib disease. Studies in Europe and the United States raise the question of whether three primary injections and one boost at around 15 months of age are sufficient, or if something more is needed to protect these populations, especially if the number or people around them who carry H. influenzae or other bacteria will not give them a boost in immunity. It has long been established that vaccine manufacturers in developing countries are able to manufacture high quality new vaccines that can satisfy WHO requisites. The Hib conjugate vaccine RIVM/NVI can offer an effective prototype for the efficacious resettlement of technology of up-to-date vaccine to the Arab Gulf and developing nations, including Saudi Arabia.

Conflict of Interests

The authors confirm that this paper content has no conflict of interests.


The current work is a part of the Ph.D. thesis of Mr. Adi Essam Zarei (Department of Biology, Faculty of Science, King Abdulaziz University). This work was supported in part by King Abdulaziz City for Scientific Research and Technology (KACST, PGP-37-56), Saudi Arabia.


  1. E. E. Adderson, C. L. Byington, L. Spencer et al., “Invasive serotype a Haemophilus influenzae infections with a virulence genotype resembling Haemophilus influenzae type b: emerging pathogen in the vaccine era?” Pediatrics, vol. 108, no. 1, article E18, 2001. View at Publisher · View at Google Scholar · View at Scopus
  2. M. G. Bruce, S. L. Deeks, T. Zulz et al., “Epidemiology of Haemophilus influenzae serotype a, North American Arctic, 2000–2005,” Emerging Infectious Diseases, vol. 14, no. 1, pp. 48–55, 2008. View at Publisher · View at Google Scholar · View at Scopus
  3. J. C. Parke Jr., R. Schneerson, and J. B. Robbins, “The attack rate, age incidence, racial distribution, and case fatality rate of Hemophilus influenzae type b meningitis in Mecklenburg County, North Carolina,” The Journal of Pediatrics, vol. 81, no. 4, pp. 765–769, 1972. View at Publisher · View at Google Scholar · View at Scopus
  4. J. N. Hanna, “The epidemiology of invasive Haemophilus influenzae infections in children under five years of age in the Northern Territory: a three-year study,” Medical Journal of Australia, vol. 152, no. 5, pp. 234–240, 1990. View at Google Scholar · View at Scopus
  5. J. I. Ward, H. S. Margolis, M. K. Lum, D. W. Fraser, T. R. Bender, and P. Anderson, “Haemophilus influenzae disease in Alaskan Eskimos: characteristics of a population with an unusual incidence of invasive disease,” The Lancet, vol. 1, no. 8233, pp. 1281–1285, 1981. View at Google Scholar
  6. S. H. Sell, R. E. Merrill, E. O. Doyne, and E. P. Zimsky Jr., “Long-term sequelae of Hemophilus influenzae meningitis,” Pediatrics, vol. 49, no. 2, pp. 206–211, 1972. View at Google Scholar · View at Scopus
  7. M. Glode, R. S. Daum, D. A. Goldmann, J. Leclair, and A. Smith, “Haemophilus influenzae type B meningitis: a contagious disease of children,” The British Medical Journal, vol. 280, no. 6218, pp. 899–901, 1980. View at Publisher · View at Google Scholar · View at Scopus
  8. M. P. Glode, M. S. Schiffer, J. B. Robbins, W. Khan, U. Battle, and E. Armenta, “An outbreak of Hemophilus influenzae type b meningitis in an enclosed hospital population,” The Journal of Pediatrics, vol. 88, no. 1, pp. 36–40, 1976. View at Publisher · View at Google Scholar · View at Scopus
  9. B. Claesson, B. Trollfors, B. Ekstrom-Jodal et al., “Incidence and prognosis of acute epiglottitis in children in a Swedish region,” Pediatric Infectious Disease, vol. 3, no. 6, pp. 534–538, 1984. View at Publisher · View at Google Scholar · View at Scopus
  10. G. J. Nabel, “Designing tomorrow's vaccines,” The New England Journal of Medicine, vol. 368, no. 6, pp. 551–560, 2013. View at Publisher · View at Google Scholar · View at Scopus
  11. F. Y. Avci, “Novel strategies for development of next-generation glycoconjugate vaccines,” Current Topics in Medicinal Chemistry, vol. 13, no. 20, pp. 2535–2540, 2013. View at Publisher · View at Google Scholar · View at Scopus
  12. B. Kuberan and R. J. Linhardt, “Carbohydrate based vaccines,” Current Organic Chemistry, vol. 4, no. 6, pp. 653–677, 2000. View at Google Scholar
  13. P. T. Heath, “Haemophilus influenzae type b conjugate vaccines: a review of efficacy data,” Pediatric Infectious Disease Journal, vol. 17, no. 9, pp. S117–S122, 1998. View at Publisher · View at Google Scholar · View at Scopus
  14. A. Zandvoort and W. Timens, “The dual function of the splenic marginal zone: essential for initiation of anti-TI-2 responses but also vital in the general first-line defense against blood-borne antigens,” Clinical and Experimental Immunology, vol. 130, no. 1, pp. 4–11, 2002. View at Publisher · View at Google Scholar · View at Scopus
  15. T. Nieminen, H. Käyhty, A. Virolainen, and J. Eskola, “Circulating antibody secreting cell response to parenteral pneumococcal vaccines as an indicator of a salivary IgA antibody response,” Vaccine, vol. 16, no. 2-3, pp. 313–319, 1998. View at Publisher · View at Google Scholar · View at Scopus
  16. Q. Zhang, S. Choo, J. Everard, R. Jennings, and A. Finn, “Mucosal immune responses to meningococcal group C conjugate and group A and C polysaccharide vaccines in adolescents,” Infection and Immunity, vol. 68, no. 5, pp. 2692–2697, 2000. View at Publisher · View at Google Scholar · View at Scopus
  17. Q. Vos, A. Lees, Z.-Q. Wu, C. M. Snapper, and J. J. Mond, “B-cell activation by T-cell-independent type 2 antigens as an integral part of the humoral immune response to pathogenic microorganisms,” Immunological Reviews, vol. 176, pp. 154–170, 2000. View at Publisher · View at Google Scholar · View at Scopus
  18. D. M. Musher, J. E. Groover, D. A. Watson et al., “Genetic regulation of the capacity to make immunoglobulin G to pneumococcal capsular polysaccharides,” Journal of Investigative Medicine, vol. 45, no. 2, pp. 57–68, 1997. View at Google Scholar · View at Scopus
  19. D. M. Granoff, R. K. Gupta, R. B. Belshe, and E. L. Andersen, “Induction of immunologic refractoriness in adults by meningococcal C polysaccharide vaccination,” Journal of Infectious Diseases, vol. 178, no. 3, pp. 870–874, 1998. View at Publisher · View at Google Scholar · View at Scopus
  20. C. B. Wilson, D. B. Lewis, and L. A. Penix, “The physiologic immunodeficiency of immaturity,” in Immunologic Disorders in Infants and Children, E. R. Stiehm, Ed., pp. 253–295, W.B. Saunders, Philadelphia, Pa, USA, 4th edition, 1996. View at Google Scholar
  21. C. Laferriere, “The immunogenicity of pneumococcal polysaccharides in infants and children: a meta-regression,” Vaccine, vol. 29, no. 40, pp. 6838–6847, 2011. View at Publisher · View at Google Scholar · View at Scopus
  22. W. S. Pomat, D. Lehmann, R. C. Sanders et al., “Immunoglobulin G antibody responses to polyvalent pneumococcal vaccine in children in the highlands of Papua New Guinea,” Infection and Immunity, vol. 62, no. 5, pp. 1848–1853, 1994. View at Google Scholar · View at Scopus
  23. B. P. Arulanandam, J. N. Mittler, W. T. Lee, M. O'Toole, and D. W. Metzger, “Neonatal administration of IL-12 enhances the protective efficacy of antiviral vaccines,” The Journal of Immunology, vol. 164, no. 7, pp. 3698–3704, 2000. View at Publisher · View at Google Scholar · View at Scopus
  24. M. O. C. Ota, J. Vekemans, S. E. Schlegel-Haueter et al., “Hepatitis B immunisation induces higher antibody and memory Th2 responses in new-borns than in adults,” Vaccine, vol. 22, no. 3-4, pp. 511–519, 2004. View at Publisher · View at Google Scholar · View at Scopus
  25. J. Rowe, C. Macaubas, T. Monger et al., “Heterogeneity in diphtheria-tetanus-acellular pertussis vaccine-specific cellular immunity during infancy: relationship to variations in the kinetics of postnatal maturation of systemic Th1 function,” Journal of Infectious Diseases, vol. 184, no. 1, pp. 80–88, 2001. View at Publisher · View at Google Scholar · View at Scopus
  26. J. Vekemans, M. O. C. Ota, E. C. Y. Wang et al., “T cell responses to vaccines in infants: defective IFNγ production after oral polio vaccination,” Clinical and Experimental Immunology, vol. 127, no. 3, pp. 495–498, 2002. View at Publisher · View at Google Scholar · View at Scopus
  27. O. J. White, K. L. McKenna, A. Bosco, A. H. J. van den Biggelaar, P. Richmond, and P. G. Holt, “A genomics-based approach to assessment of vaccine safety and immunogenicity in children,” Vaccine, vol. 30, no. 10, pp. 1865–1874, 2012. View at Publisher · View at Google Scholar · View at Scopus
  28. O. J. White, J. Rowe, P. Richmond et al., “Th2-polarisation of cellular immune memory to neonatal pertussis vaccination,” Vaccine, vol. 28, no. 14, pp. 2648–2652, 2010. View at Publisher · View at Google Scholar · View at Scopus
  29. C.-A. Siegrist, “Neonatal and early life vaccinology,” Vaccine, vol. 19, no. 25-26, pp. 3331–3346, 2001. View at Publisher · View at Google Scholar · View at Scopus
  30. A. Finn, “Bacterial polysaccharide-protein conjugate vaccines,” British Medical Bulletin, vol. 70, pp. 1–14, 2004. View at Publisher · View at Google Scholar · View at Scopus
  31. G. Swingler, D. Fransman, and G. Hussey, “Conjugate vaccines for preventing Haemophilus influenzae type b infections,” Cochrane Database of Systematic Reviews, vol. 4, Article ID CD001729, 2003. View at Google Scholar
  32. P. T. Heath, R. Booy, H. Griffiths et al., “Clinical and immunological risk factors associated with haemophilus influenzae type b conjugate vaccine failure in childhood,” Clinical Infectious Diseases, vol. 31, no. 4, pp. 973–980, 2000. View at Publisher · View at Google Scholar · View at Scopus
  33. S. R. Dominguez and R. S. Daum, “Toward global Haemophilus influenzae type b immunization,” Clinical Infectious Diseases, vol. 37, no. 12, pp. 1600–1602, 2003. View at Publisher · View at Google Scholar · View at Scopus
  34. R. T. Mahoney and J. E. Maynard, “The introduction of new vaccines into developing countries,” Vaccine, vol. 17, no. 7-8, pp. 646–652, 1999. View at Publisher · View at Google Scholar · View at Scopus
  35. A. Arvas, E. Gur, H. Bahar et al., “Haemophilus influenzae type b antibodies in vaccinated and non-vaccinated children,” Pediatrics International, vol. 50, no. 4, pp. 469–473, 2008. View at Publisher · View at Google Scholar · View at Scopus
  36. M. Almuneef, M. Alshaalan, Z. Memish, and S. Alalola, “Bacterial meningitis in Saudi Arabia: the impact of Haemophilus influenzae type b vaccination,” Journal of Chemotherapy, vol. 13, supplement 1, pp. 34–39, 2001. View at Publisher · View at Google Scholar · View at Scopus
  37. F. A. Al-Zamil, “Conjugated pneumococcal vaccine for children in Saudi Arabia: following the footsteps of hib vaccine,” The Journal of the Egyptian Public Health Association, vol. 83, no. 1-2, pp. 35–47, 2008. View at Google Scholar
  38. Health Statistic Annual Book: Kingdom of Saudi Arabia Ministry of Health, 2013,
  39. Global Programme for Vaccines and Immunization (GPV), “The WHO position paper on Haemophilus influenzae type b conjugate vaccines,” The Weekly Epidemiological Record, vol. 73, no. 10, pp. 64–68, 1998. View at Google Scholar
  40. M. Finland and W. D. Sutliff, “Specific antibody response of human subjects to intracutaneous injection of pneumococcus products,” The Journal of Experimental Medicine, vol. 55, no. 6, pp. 853–865, 1932. View at Publisher · View at Google Scholar
  41. C. L. Hoagland, P. B. Beeson, and W. F. Goebel, “The capsular polysaccharide of the type XIV pneumococcus and its relationship to the specific substances of human blood,” Science, vol. 88, no. 2281, pp. 261–263, 1938. View at Publisher · View at Google Scholar · View at Scopus
  42. H. Kayhty, V. Karanko, H. Peltola, and P. H. Makela, “Serum antibodies after vaccination with Haemophilus influenzae type b capsular polysaccharide and responses to reimmunization: no evidence of immunologic tolerance or memory,” Pediatrics, vol. 74, no. 5, pp. 857–865, 1984. View at Google Scholar · View at Scopus
  43. J. B. Robbins and R. Schneerson, “Polysaccharide-protein conjugates: a new generation of vaccines,” The Journal of Infectious Diseases, vol. 161, no. 5, pp. 821–832, 1990. View at Publisher · View at Google Scholar · View at Scopus
  44. J. I. Ward, C. V. Broome, L. H. Harrison, H. Shinefield, and S. Black, “Haemophilus influenzae type b vaccines: lessons for the future,” Pediatrics, vol. 81, no. 6, pp. 886–893, 1988. View at Google Scholar · View at Scopus
  45. H. Kayhty, H. Peltola, V. Karanko, and P. H. Makela, “The protective level of serum antibodies to the capsular polysaccharide of Haemophilus influenzae type b,” Journal of Infectious Diseases, vol. 147, no. 6, p. 1100, 1983. View at Publisher · View at Google Scholar · View at Scopus
  46. R. Z. Dintzis, M. Okajima, M. H. Middleton, G. Greene, and H. M. Dintzis, “The immunogenicity of soluble haptenated polymers is determined by molecular mass and hapten valence,” The Journal of Immunology, vol. 143, no. 4, pp. 1239–1244, 1989. View at Google Scholar · View at Scopus
  47. J. C. Aguilar and E. G. Rodríguez, “Vaccine adjuvants revisited,” Vaccine, vol. 25, no. 19, pp. 3752–3762, 2007. View at Publisher · View at Google Scholar · View at Scopus
  48. B. Guy, “Adjuvants for protein- and carbohydrate-based vaccines,” in Carbohydrate-Based Vaccines and Immunotherapies, pp. 89–115, John Wiley & Sons, New York, NY, USA, 2008. View at Google Scholar
  49. T. A. Barr, J. Carlring, and A. W. Heath, “Co-stimulatory agonists as immunological adjuvants,” Vaccine, vol. 24, no. 17, pp. 3399–3407, 2006. View at Publisher · View at Google Scholar · View at Scopus
  50. E. C. Briere, L. Rubin, P. L. Moro, A. Cohn, T. Clark, and N. Messonnier, “Prevention and control of haemophilus influenzae type b disease: recommendations of the advisory committee on immunization practices (ACIP),” Morbidity and Mortality Weekly Report, vol. 63, no. 1, pp. 1–14, 2014. View at Google Scholar
  51. R. Z. Dintzis, “Rational design of conjugate vaccines,” Pediatric Research, vol. 32, no. 4, pp. 376–385, 1992. View at Publisher · View at Google Scholar · View at Scopus
  52. K. E. Stein, “Glycoconjugate vaccines. What next?” International Journal of Technology Assessment in Health Care, vol. 10, no. 1, pp. 167–176, 1994. View at Publisher · View at Google Scholar · View at Scopus
  53. A. A. Lindberg, “Glycoprotein conjugate vaccines,” Vaccine, vol. 17, supplement 2, pp. S28–S36, 1999. View at Publisher · View at Google Scholar · View at Scopus
  54. J. L. Hsu, “A brief history of vaccines: smallpox to the present,” South Dakota Medicine, Special no. 33–37, 2013. View at Google Scholar
  55. S. A. Plotkin and S. L. Plotkin, “The development of vaccines: how the past led to the future,” Nature Reviews Microbiology, vol. 9, no. 12, pp. 889–893, 2011. View at Publisher · View at Google Scholar · View at Scopus
  56. A. H. J. van den Biggelaar and W. S. Pomat, “Immunization of newborns with bacterial conjugate vaccines,” Vaccine, vol. 31, no. 21, pp. 2525–2530, 2013. View at Publisher · View at Google Scholar · View at Scopus
  57. W. E. Dick Jr. and M. Beurret, “Glycoconjugates of bacterial carbohydrate antigens. A survey and consideration of design and preparation factors,” Contributions to Microbiology and Immunology, vol. 10, pp. 48–114, 1989. View at Google Scholar · View at Scopus
  58. A. Lees, V. Puvanesarajah, and C. E. Frasch, “Conjugation chemistry,” in Pneumococcal Vaccines, pp. 163–174, American Society of Microbiology, 2008. View at Google Scholar
  59. W. Zou and H. J. Jennings, “Preparation of glycoconjugate vaccines,” in Carbohydrate-Based Vaccines and Immunotherapies, Z. Guo and G.-J. Boons, Eds., John Wiley & Sons, New York, NY, USA, 2009. View at Publisher · View at Google Scholar
  60. G. Toraño, M. E. Toledo, A. Baly et al., “Phase I clinical evaluation of a synthetic oligosaccharide-protein conjugate vaccine against Haemophilus influenzae type b in human adult volunteers,” Clinical and Vaccine Immunology, vol. 13, no. 9, pp. 1052–1056, 2006. View at Publisher · View at Google Scholar · View at Scopus
  61. S. Bay, V. Huteau, M.-L. Zarantonelli et al., “Phosphorylcholine-carbohydrate-protein conjugates efficiently induce hapten-specific antibodies which recognize both Streptococcus pneumoniae and Neisseria meningitidis: a potential multitarget vaccine against respiratory infections,” Journal of Medicinal Chemistry, vol. 47, no. 16, pp. 3916–3919, 2004. View at Publisher · View at Google Scholar · View at Scopus
  62. T. Buskas, Y. Li, and G. J. Boons, “The immunogenicity of the tumor-associated antigen Lewis(y) may be suppressed by a bifunctional cross-linker required for coupling to a carrier protein,” Chemistry, vol. 10, no. 14, pp. 3517–3524, 2004. View at Publisher · View at Google Scholar
  63. P. H. Seeberger, R. L. Soucy, Y.-U. Kwon, D. A. Snyder, and T. Kanemitsu, “A convergent, versatile route to two synthetic conjugate anti-toxin malaria vaccines,” Chemical Communications, vol. 10, no. 15, pp. 1706–1707, 2004. View at Google Scholar · View at Scopus
  64. V. Verez-Bencomo, V. Fernández-Santana, E. Hardy et al., “A synthetic conjugate polysaccharide vaccine against Haemophilus influenzae type b,” Science, vol. 305, no. 5683, pp. 522–525, 2004. View at Publisher · View at Google Scholar · View at Scopus
  65. C. C. A. M. Peeters, A.-M. J. Tenbergen-Meekes, J. T. Poolman, B. J. M. Zegers, and G. T. Rijkers, “Immunogenicity of a Streptococcus pneumoniae type 4 polysaccharide-protein conjugate vaccine is decreased by admixture of high doses of free saccharide,” Vaccine, vol. 10, no. 12, pp. 833–840, 1992. View at Publisher · View at Google Scholar · View at Scopus
  66. M. E. Rodriguez, G. P. J. M. van den Dobbelsteen, L. A. Oomen et al., “Immunogenicity of Streptococcus pneumoniae type 6B and 14 polysaccharide-tetanus toxoid conjugates and the effect of uncoupled polysaccharide on the antigen-specific immune response,” Vaccine, vol. 16, no. 20, pp. 1941–1949, 1998. View at Publisher · View at Google Scholar · View at Scopus
  67. G. R. Gray, “Antibodies to carbohydrates: preparation of antigens by coupling carbohydrates to proteins by reductive amination with cyanoborohydride,” Methods in Enzymology, vol. 50, pp. 155–160, 1978. View at Publisher · View at Google Scholar
  68. B. A. Schwartz and G. R. Gray, “Proteins containing reductively aminated disaccharides. Synthesis and chemical characterization,” Archives of Biochemistry and Biophysics, vol. 181, no. 2, pp. 542–549, 1977. View at Publisher · View at Google Scholar · View at Scopus
  69. M. L. C. Da Silva, T. Tamura, T. McBroom, and K. G. Rice, “Tyrosine derivatization and preparative purification of the sialyl and asialyl N-linked oligosaccharides from porcine fibrinogen,” Archives of Biochemistry and Biophysics, vol. 312, no. 1, pp. 151–157, 1994. View at Publisher · View at Google Scholar · View at Scopus
  70. S. Y. C. Wong, G. R. Guile, R. A. Dwek, and G. Arsequell, “Synthetic glycosylation of proteins using N-(β-saccharide) iodoacetamides: applications in site-specific glycosylation and solid-phase enzymic oligosaccharide synthesis,” Biochemical Journal, vol. 300, no. 3, pp. 843–850, 1994. View at Publisher · View at Google Scholar · View at Scopus
  71. S. Y. C. Wong, G. R. Guile, T. W. Rademacher, and R. A. Dwek, “Synthetic glycosylation of peptides using unprotected saccharide beta-glycosylamines,” Glycoconjugate Journal, vol. 10, no. 3, pp. 227–234, 1993. View at Google Scholar · View at Scopus
  72. G. Ragupathi, R. R. Koganty, D. Qiu, K. O. Lloyd, and P. O. Livingston, “A novel and efficient method for synthetic carbohydrate conjugate vaccine preparation: synthesis of sialyl Tn-KLH conjugate using a 4-(4-N-maleimidomethyl) cyclohexane-1-carboxyl hydrazide (MMCCH) linker arm,” Glycoconjugate Journal, vol. 15, no. 3, pp. 217–221, 1998. View at Publisher · View at Google Scholar · View at Scopus
  73. E. C. Beuvery, G. J. Speijers, B. I. Lutz et al., “Analytical, toxicological and immunological consequences of the use of N-ethyl-N′-(3-dimethylaminopropyl) carbodiimide as coupling reagent for the preparation of meningococcal group C polysaccharide-tetanus toxoid conjugate as vaccine for human use,” Developments in Biological Standardization, vol. 63, pp. 117–128, 1986. View at Google Scholar
  74. J. V. Staros, R. W. Wright, and D. M. Swingle, “Enhancement by N-hydroxysulfosuccinimide of water-soluble carbodiimide-mediated coupling reactions,” Analytical Biochemistry, vol. 156, no. 1, pp. 220–222, 1986. View at Publisher · View at Google Scholar · View at Scopus
  75. O. T. Avery and W. F. Goebel, “Chemo-immunological studies on conjugated carbohydrate-proteins: V. The immunological specifity of an antigen prepared by combining the capsular polysaccharide of type III pneumococcus with foreign protein,” The Journal of Experimental Medicine, vol. 54, no. 3, pp. 437–447, 1931. View at Publisher · View at Google Scholar
  76. R. Axén, J. Porath, and S. Ernback, “Chemical coupling of peptides and proteins to polysaccharides by means of cyanogen halides,” Nature, vol. 214, no. 5095, pp. 1302–1304, 1967. View at Publisher · View at Google Scholar · View at Scopus
  77. L. Chi-Jen, “Bacterial capsular polysaccharides—biochemistry, immunity and vaccine,” Molecular Immunology, vol. 24, no. 10, pp. 1005–1019, 1987. View at Publisher · View at Google Scholar · View at Scopus
  78. L. C. Paoletti, M. A. Rench, D. L. Kasper, D. Molrine, D. Ambrosino, and C. J. Baker, “Effects of alum adjuvant or a booster dose on immunogenicity during clinical trials of group B streptococcal type III conjugate vaccines,” Infection and Immunity, vol. 69, no. 11, pp. 6696–6701, 2001. View at Publisher · View at Google Scholar
  79. A. W. Sturgess, K. Rush, R. J. Charbonneau et al., “Haemophilus influenzae type b conjugate vaccine stability: catalytic depolymerization of PRP in the presence of aluminum hydroxide,” Vaccine, vol. 17, no. 9-10, pp. 1169–1178, 1999. View at Publisher · View at Google Scholar · View at Scopus
  80. R. S. Chu, T. McCool, N. S. Greenspan, J. R. Schreiber, and C. V. Harding, “CpG oligodeoxynucleotides act as adjuvants for pneumococcal polysaccharide-protein conjugate vaccines and enhance antipolysaccharide immunoglobulin G2a (IgG2a) and IgG3 antibodies,” Infection and Immunity, vol. 68, no. 3, pp. 1450–1456, 2000. View at Publisher · View at Google Scholar · View at Scopus
  81. T. A. Olafsdottir, S. G. Hannesdottir, G. D. Giudice, E. Trannoy, and I. Jonsdottir, “Effects of LT-K63 and CpG2006 on phenotype and function of murine neonatal lymphoid cells,” Scandinavian Journal of Immunology, vol. 66, no. 4, pp. 426–434, 2007. View at Publisher · View at Google Scholar · View at Scopus
  82. G. Sen, Q. Chen, and C. M. Snapper, “Immunization of aged mice with a pneumococcal conjugate vaccine combined with an unmethylated CpG-containing oligodeoxynucleotide restores defective immunoglobulin G antipolysaccharide responses and specific CD4+-T-cell priming to young adult levels,” Infection and Immunity, vol. 74, no. 4, pp. 2177–2186, 2006. View at Publisher · View at Google Scholar · View at Scopus
  83. T. Barington, M. Skettrup, L. Juul, and C. Heilmann, “Non-epitope-specific suppression of the antibody response to Haemophilus influenzae type b conjugate vaccines by preimmunization with vaccine components,” Infection and Immunity, vol. 61, no. 2, pp. 432–438, 1993. View at Google Scholar · View at Scopus
  84. A. Fattom, Y. H. Cho, C. Chu, S. Fuller, L. Fries, and R. Naso, “Epitopic overload at the site of injection may result in suppression of the immune response to combined capsular polysaccharide conjugate vaccines,” Vaccine, vol. 17, no. 2, pp. 126–133, 1999. View at Publisher · View at Google Scholar · View at Scopus
  85. M.-P. Schutze, E. Deriaud, G. Przewlocki, and C. LeClerc, “Carrier-induced epitopic suppression is initiated through clonal dominance,” The Journal of Immunology, vol. 142, no. 8, pp. 2635–2640, 1989. View at Google Scholar · View at Scopus
  86. Organization WHO, “Recommendations for the production and control of Haemophilus influenzae type b conjugate vaccines,” WHO Technical Report Series, no. 897, pp. 27–60, 2000. View at Google Scholar
  87. World Health Organization, “WHO position paper on Haemophilus influenzae type b conjugate vaccines. (Replaces WHO position paper on Hib vaccines previously published in the Weekly Epidemiological Record,” The Weekly Epidemiological Record, vol. 81, no. 47, pp. 445–452, 2006. View at Google Scholar
  88. “Progress introducing Haemophilus influenzae type b vaccine in low-income countries, 2004–2008,” Weekly Epidemiological Record, vol. 83, no. 7, pp. 61–67, 2008.
  89. B. D. Gessner, A. Sutanto, M. Linehan et al., “Incidences of vaccine-preventable Haemophilus influenzae type b pneumonia and meningitis in Indonesian children: hamlet-randomised vaccine-probe trial,” The Lancet, vol. 365, no. 9453, pp. 43–52, 2005. View at Publisher · View at Google Scholar · View at Scopus
  90. H. Peltola, “Worldwide Haemophilus influenzae type b disease at the beginning of the 21st century: Global analysis of the disease burden 25 years after the use of the polysaccharide vaccine and a decade after the advent of conjugates,” Clinical Microbiology Reviews, vol. 13, no. 2, pp. 302–317, 2000. View at Publisher · View at Google Scholar · View at Scopus
  91. O. S. Levine, B. Schwartz, N. Pierce, and M. Kane, “Development, evaluation and implementation of Haemophilus influenzae type b vaccines for young children in developing countries: current status and priority actions,” The Pediatric Infectious Disease Journal, vol. 17, no. 9, supplement, pp. S95–S113, 1998. View at Publisher · View at Google Scholar · View at Scopus
  92. Lessons learned: new procurement strategies for vaccines. Final report to the GAVI board, GAVI Alliance: Mercer Management Consulting, 2002,
  93. M. C. Danovaro-Holliday, S. Garcia, C. de Quadros, G. Tambini, and J. K. Andrus, “Progress in vaccination against Haemophilus influenzae type b in the Americas,” PLoS Medicine, vol. 5, no. 4, article e87, 2008. View at Publisher · View at Google Scholar · View at Scopus
  94. M. Landaverde, J. L. Di Fabio, G. Ruocco, I. Leal, and C. de Quadros, “Introduction of a conjugate vaccine against Hib in Chile and Uruguay,” Revista Panamericana de Salud Pública, vol. 5, no. 3, pp. 200–206, 1999. View at Publisher · View at Google Scholar
  95. J. D. Wenger, J.-L. DiFabio, J. M. Landaverde, O. S. Levine, and T. Gaafar, “Introduction of Hib conjugate vaccines in the non-industrialized world: experience in four ‘newly adopting’ countries,” Vaccine, vol. 18, no. 7-8, pp. 736–742, 1999. View at Publisher · View at Google Scholar · View at Scopus
  96. A. Hamidi, C. Boog, S. Jadhav, and H. Kreeftenberg, “Lessons learned during the development and transfer of technology related to a new Hib conjugate vaccine to emerging vaccine manufacturers,” Vaccine, vol. 32, no. 33, pp. 4124–4130, 2014. View at Publisher · View at Google Scholar · View at Scopus
  97. J. B. Milstien, P. Gaulé, and M. Kaddar, “Access to vaccine technologies in developing countries: Brazil and India,” Vaccine, vol. 25, no. 44, pp. 7610–7619, 2007. View at Publisher · View at Google Scholar · View at Scopus
  98. M. Beurret, A. Hamidi, and H. Kreeftenberg, “Development and technology transfer of Haemophilus influenzae type b conjugate vaccines for developing countries,” Vaccine, vol. 30, no. 33, pp. 4897–4906, 2012. View at Publisher · View at Google Scholar · View at Scopus
  99. F. Mawas, G. Newman, S. Burns, and M. J. Corbel, “Suppression and modulation of cellular and humoral immune responses to Haemophilus influenzae type B (Hib) conjugate vaccine in Hib-diphtheria-tetanus toxoids-acellular pertussis combination vaccines: a study in a rat model,” Journal of Infectious Diseases, vol. 191, no. 1, pp. 58–64, 2005. View at Publisher · View at Google Scholar · View at Scopus
  100. Arabio Company, 2006,
  101. S. A. Plotkin, “Vaccines: the fourth century,” Clinical and Vaccine Immunology, vol. 16, no. 12, pp. 1709–1719, 2009. View at Publisher · View at Google Scholar · View at Scopus
  102. G. M. Glenn, D. N. Taylor, X. Li, S. Frankel, A. Montemarano, and C. R. Alving, “Transcutaneous immunization: a human vaccine delivery strategy using a patch,” Nature Medicine, vol. 6, no. 12, pp. 1403–1406, 2000. View at Publisher · View at Google Scholar · View at Scopus
  103. A.-S. Beignon, J.-P. Briand, S. Muller, and C. D. Partidos, “Immunization onto bare skin with heat-labile enterotoxin of Escherichia coli enhances immune responses to coadministered protein and peptide antigens and protects mice against lethal toxin challenge,” Immunology, vol. 102, no. 3, pp. 344–351, 2001. View at Publisher · View at Google Scholar · View at Scopus
  104. A.-S. Beignon, J.-P. Briand, R. Rappuoli, S. Muller, and C. D. Partidos, “The LTR72 mutant of heat-labile enterotoxin of Escherichia coli enhances the ability of peptide antigens to elicit CD4+ T cells and secrete gamma interferon after coapplication onto bare skin,” Infection and Immunity, vol. 70, no. 6, pp. 3012–3019, 2002. View at Publisher · View at Google Scholar · View at Scopus
  105. G. M. Glenn, T. Scharton-Kersten, R. Vassell, C. P. Mallett, T. L. Hale, and C. R. Alving, “Transcutaneous immunization with cholera toxin protects mice against lethal mucosal toxin challenge,” The Journal of Immunology, vol. 161, no. 7, pp. 3211–3214, 1998. View at Google Scholar · View at Scopus
  106. C. M. Gockel, S. Bao, and K. W. Beagley, “Transcutaneous immunization induces mucosal and systemic immunity: a potent method for targeting immunity to the female reproductive tract,” Molecular Immunology, vol. 37, no. 9, pp. 537–544, 2000. View at Publisher · View at Google Scholar · View at Scopus
  107. S. Godefroy, L. Goestch, H. Plotnicky-Gilquin et al., “Immunization onto shaved skin with a bacterial enterotoxin adjuvant protects mice against Respiratory Syncytial Virus (RSV),” Vaccine, vol. 21, no. 15, pp. 1665–1671, 2003. View at Publisher · View at Google Scholar · View at Scopus
  108. R. Tierney, A.-S. Beignon, R. Rappuoli, S. Muller, D. Sesardic, and C. Partidos, “Transcutaneous immunization with tetanus toxoid and mutants of Escherichia coli heat-labile enterotoxin as adjuvants elicits strong protective antibody responses,” Journal of Infectious Diseases, vol. 188, no. 5, pp. 753–758, 2003. View at Publisher · View at Google Scholar · View at Scopus
  109. B. Quiambao, O. Van Der Meeren, D. Kolhe, and S. Gatchalian, “A randomized, dose-ranging assessment of the immunogenicity and safety of a booster dose of a combined diphtheria-tetanus-whole cell pertussis-hepatitis B-inactivated poliovirus-Hemophilus influenzae type b (DTPw-HBV-IPV/Hib) vaccine vs. co-administration of DTPw-HBV/Hib and IPV vaccines in 12 to 24 months old Filipino toddlers,” Human Vaccines & Immunotherapeutics, vol. 8, no. 3, pp. 347–354, 2012. View at Publisher · View at Google Scholar · View at Scopus
  110. H. Kalies, V. Grote, T. Verstraeten, L. Hessel, H.-J. Schmitt, and R. Von Kries, “The use of combination vaccines has improved timeliness of vaccination in children,” Pediatric Infectious Disease Journal, vol. 25, no. 6, pp. 507–512, 2006. View at Publisher · View at Google Scholar · View at Scopus
  111. L. E. Happe, O. E. Lunacsek, D. T. Kruzikas, and G. S. Marshall, “Impact of a pentavalent combination vaccine on immunization timeliness in a state medicaid population,” Pediatric Infectious Disease Journal, vol. 28, no. 2, pp. 98–101, 2009. View at Publisher · View at Google Scholar · View at Scopus
  112. V. Baldo, P. Bonanni, M. Castro et al., “Combined hexavalent diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated poliovirus-Hemophilus influenzae type b vaccine; Infanrix hexa: twelve years of experience in Italy,” Human Vaccines and Immunotherapeutics, vol. 10, no. 1, pp. 129–137, 2014. View at Publisher · View at Google Scholar · View at Scopus
  113. H. Kalies, V. Grote, A. Siedler, B. Gröndahl, H.-J. Schmitt, and R. von Kries, “Effectiveness of hexavalent vaccines against invasive Haemophilus influenzae type b disease: Germany's experience after 5 years of licensure,” Vaccine, vol. 26, no. 20, pp. 2545–2552, 2008. View at Publisher · View at Google Scholar · View at Scopus
  114. H. O. Hallander, T. Lepp, M. Ljungman, E. Netterlid, and M. Andersson, “Do we need a booster of Hib vaccine after primary vaccination? A study on anti-Hib seroprevalence in Sweden 5 and 15 years after the introduction of universal Hib vaccination related to notifications of invasive disease,” APMIS, vol. 118, no. 11, pp. 878–887, 2010. View at Publisher · View at Google Scholar · View at Scopus
  115. M. S. Amstey, R. Insel, J. Munoz, and M. Pichichero, “Fetal-neonatal passive immunization against Hemophilus influenzae, type b,” American Journal of Obstetrics and Gynecology, vol. 153, no. 6, pp. 607–611, 1985. View at Publisher · View at Google Scholar · View at Scopus
  116. J. A. Englund, W. P. Glezen, C. Turner, J. Harvey, C. Thompson, and G. R. Siber, “Transplacental antibody transfer following maternal immunization with polysaccharide and conjugate Haemophilus influenzae type b vaccines,” Journal of Infectious Diseases, vol. 171, no. 1, pp. 99–105, 1995. View at Publisher · View at Google Scholar · View at Scopus
  117. M. S. Einhorn, D. M. Granoff, M. H. Nahm, A. Quinn, and P. G. Shackelford, “Concentrations of antibodies in paired maternal and infant sera: relationship to IgG subclass,” The Journal of Pediatrics, vol. 111, no. 5, pp. 783–788, 1987. View at Publisher · View at Google Scholar · View at Scopus
  118. M. K. Park, J. A. Englund, W. P. Glezen, G. R. Siber, and M. H. Nahm, “Association of placental transfer of anti-Haemophilus influenzae type b polysaccharide antibodies with their V regions,” Vaccine, vol. 14, no. 13, pp. 1219–1222, 1996. View at Publisher · View at Google Scholar · View at Scopus
  119. A. M. Krieg, “Lymphocyte activation by CpG dinucleotide motifs in prokaryotic DNA,” Trends in Microbiology, vol. 4, no. 2, pp. 73–77, 1996. View at Publisher · View at Google Scholar · View at Scopus
  120. V. E. Schijns, “Immunological concepts of vaccine adjuvant activity,” Current Opinion in Immunology, vol. 12, no. 4, pp. 456–463, 2000. View at Publisher · View at Google Scholar · View at Scopus
  121. C. A. Janeway Jr. and R. Medzhitov, “Introduction: the role of innate immunity in the adaptive immune response,” Seminars in Immunology, vol. 10, no. 5, pp. 349–350, 1998. View at Publisher · View at Google Scholar · View at Scopus
  122. M. Roman, E. Martin-Orozco, J. S. Goodman et al., “Immunostimulatory DNA sequences function as T helper-1-promoting adjuvants,” Nature Medicine, vol. 3, no. 8, pp. 849–854, 1997. View at Publisher · View at Google Scholar · View at Scopus
  123. N. S. Greenspan and L. J. N. Cooper, “Intermolecular cooperativity: a clue to why mice have IgG3?” Immunology Today, vol. 13, no. 5, pp. 164–168, 1992. View at Publisher · View at Google Scholar · View at Scopus
  124. F. D. Finkelman, J. Holmes, I. M. Katona et al., “Lymphokine control of in vivo immunoglobulin isotype selection,” Annual Review of Immunology, vol. 8, pp. 303–333, 1990. View at Publisher · View at Google Scholar · View at Scopus
  125. A. R. Foxwell, J. M. Kyd, and A. W. Cripps, “Nontypeable Haemophilus influenzae: pathogenesis and prevention,” Microbiology and Molecular Biology Reviews, vol. 62, no. 2, pp. 294–308, 1998. View at Google Scholar · View at Scopus
  126. M. R. Loeb and D. H. Smith, “Outer membrane protein composition in disease isolates of Haemophilus influenzae: pathogenic and epidemiological implications,” Infection and Immunity, vol. 30, no. 3, pp. 709–717, 1980. View at Google Scholar · View at Scopus
  127. S. J. Barenkamp, R. S. Munson Jr., and D. M. Granoff, “Subtyping isolates of Haemophilus influenzae type b by outer-membrane protein profiles,” The Journal of Infectious Diseases, vol. 143, no. 5, pp. 668–676, 1981. View at Publisher · View at Google Scholar · View at Scopus
  128. M. Comanducci, S. Bambini, B. Brunelli et al., “NadA, a novel vaccine candidate of Neisseria meningitidis,” Journal of Experimental Medicine, vol. 195, no. 11, pp. 1445–1454, 2002. View at Publisher · View at Google Scholar · View at Scopus
  129. C. A. Janeway, P. Travers, M. Walport, and M. Chlomchik, Immunobiology, Garland Science Publishing, New York, NY, USA, 6th edition, 2005.
  130. N. A. Mitchison, “T-cell-B-cell cooperation,” Nature Reviews Immunology, vol. 4, no. 4, pp. 308–312, 2004. View at Publisher · View at Google Scholar
  131. F. Y. Avci and D. L. Kasper, “How bacterial carbohydrates influence the adaptive immune system,” Annual Review of Immunology, vol. 28, pp. 107–130, 2010. View at Publisher · View at Google Scholar · View at Scopus
  132. B. A. Cobb, Q. Wang, A. O. Tzianabos, and D. L. Kasper, “Polysaccharide processing and presentation by the MHCII pathway,” Cell, vol. 117, no. 5, pp. 677–687, 2004. View at Publisher · View at Google Scholar · View at Scopus
  133. Á. G. Barrientos, J. M. de la Fuente, T. C. Rojas, A. Fernández, and S. Penadés, “Gold glyconanoparticles: synthetic polyvalent ligands mimicking glycocalyx-like surfaces as tools for glycobiological studies,” Chemistry—A European Journal, vol. 9, no. 9, pp. 1909–1921, 2003. View at Publisher · View at Google Scholar · View at Scopus
  134. F. Y. Avci, X. Li, M. Tsuji, and D. L. Kasper, “A mechanism for glycoconjugate vaccine activation of the adaptive immune system and its implications for vaccine design,” Nature Medicine, vol. 17, no. 12, pp. 1602–1609, 2011. View at Publisher · View at Google Scholar · View at Scopus
  135. H. Amir-Kroll, L. Riveron, M. E. Sarmiento, G. Sierra, A. Acosta, and I. R. Cohen, “A conjugate vaccine composed of a heat shock protein 60 T-cell epitope peptide (p458) and Neisseria meningitidis type B capsular polysaccharide,” Vaccine, vol. 24, no. 42-43, pp. 6555–6563, 2006. View at Publisher · View at Google Scholar · View at Scopus
  136. N. Cohen, M. Stolarsky-Bennun, H. Amir-Kroll et al., “Pneumococcal capsular polysaccharide is immunogenic when present on the surface of macrophages and dendritic cells: TLR4 signaling induced by a conjugate vaccine or by lipopolysaccharide is conducive,” The Journal of Immunology, vol. 180, no. 4, pp. 2409–2418, 2008. View at Publisher · View at Google Scholar · View at Scopus
  137. S. Könen-Waisman, A. Cohen, M. Fridkin, and I. R. Cohen, “Self heat-shock protein (hsp60) peptide serves in a conjugate vaccine against a lethal pneumococcal infection,” Journal of Infectious Diseases, vol. 179, no. 2, pp. 403–413, 1999. View at Publisher · View at Google Scholar · View at Scopus
  138. F. Falugi, R. Petracca, M. Mariani et al., “Rationally designed strings of promiscuous CD4+ T cell epitopes provide help to Haemophilus influenzae type b oligosaccharide: a model for new conjugate vaccines,” European Journal of Immunology, vol. 31, no. 12, pp. 3816–3824, 2001. View at Publisher · View at Google Scholar · View at Scopus
  139. K. Baraldo, E. Mori, A. Bartoloni et al., “Combined conjugate vaccines: enhanced immunogenicity with the N19 polyepitope as a carrier protein,” Infection and Immunity, vol. 73, no. 9, pp. 5835–5841, 2005. View at Publisher · View at Google Scholar · View at Scopus
  140. R. Rana, J. Dalal, D. Singh et al., “Development and characterization of Haemophilus influenzae type b conjugate vaccine prepared using different polysaccharide chain lengths,” Vaccine, vol. 33, no. 23, pp. 2646–2654, 2015. View at Publisher · View at Google Scholar
  141. A. Bardotti, G. Averani, F. Berti et al., “Physicochemical characterisation of glycoconjugate vaccines for prevention of meningococcal diseases,” Vaccine, vol. 26, no. 18, pp. 2284–2296, 2008. View at Publisher · View at Google Scholar · View at Scopus
  142. M. Bröker, P. M. Dull, R. Rappuoli, and P. Costantino, “Chemistry of a new investigational quadrivalent meningococcal conjugate vaccine that is immunogenic at all ages,” Vaccine, vol. 27, no. 41, pp. 5574–5580, 2009. View at Publisher · View at Google Scholar · View at Scopus
  143. P. Costantino, R. Rappuoli, and F. Berti, “The design of semi-synthetic and synthetic glycoconjugate vaccines,” Expert Opinion on Drug Discovery, vol. 6, no. 10, pp. 1045–1066, 2011. View at Publisher · View at Google Scholar · View at Scopus
  144. E. Altindis, “Antibacterial vaccine research in 21st century: from inoculation to genomics approaches,” Current Topics in Medicinal Chemistry, vol. 13, no. 20, pp. 2638–2646, 2013. View at Publisher · View at Google Scholar · View at Scopus
  145. M. N. Baeshen, A. M. Al-Hejin, R. S. Bora et al., “Production of biopharmaceuticals in E. coli: current scenario and future perspectives,” Journal of Microbiology and Biotechnology, vol. 25, no. 7, pp. 953–962, 2015. View at Publisher · View at Google Scholar
  146. N. A. Baeshen, M. N. Baeshen, A. Sheikh et al., “Cell factories for insulin production,” Microbial Cell Factories, vol. 13, article 141, 2014. View at Publisher · View at Google Scholar · View at Scopus
  147. N. A. El-Baky and E. M. Redwan, “Therapeutic alpha-interferons protein: structure, production, and biosimilar,” Preparative Biochemistry & Biotechnology, vol. 45, no. 2, pp. 109–127, 2015. View at Publisher · View at Google Scholar · View at Scopus
  148. N. A. El-Baky, V. N. Uversky, and E. M. Redwan, “Human consensus interferons: bridging the natural and artificial cytokines with intrinsic disorder,” Cytokine & Growth Factor Reviews, vol. 26, no. 6, pp. 637–645, 2015. View at Publisher · View at Google Scholar
  149. E.-R. M. Redwan, “Cumulative updating of approved biopharmaceuticals,” Human Antibodies, vol. 16, no. 3-4, pp. 137–158, 2007. View at Google Scholar · View at Scopus
  150. E.-R. M. Redwan, “Animal-derived pharmaceutical proteins,” Journal of Immunoassay and Immunochemistry, vol. 30, no. 3, pp. 262–290, 2009. View at Publisher · View at Google Scholar · View at Scopus
  151. Y. Liao, E. M. El-Fakkarany, B. Lönnerdal, and E. M. Redwan, “Inhibitory effects of native/recombinant full-length camel lactoferrin and its N/C lobes on hepatitis C virus infection of Huh7.5 cells,” Journal of Medical Microbiology, vol. 61, part 3, pp. 375–383, 2012. View at Publisher · View at Google Scholar
  152. E.-R. M. Redwan, A. Fahmy, A. E. Hanafy, N. A. EL-Baky, and S. M. A. Sallam, “Ovine anti-rabies antibody production and evaluation,” Comparative Immunology, Microbiology and Infectious Diseases, vol. 32, no. 1, pp. 9–19, 2009. View at Publisher · View at Google Scholar · View at Scopus
  153. E.-R. M. Redwan, S. M. Matar, G. A. El-Aziz, and E. A. Serour, “Synthesis of the human insulin gene: protein expression, scaling up and bioactivity,” Preparative Biochemistry and Biotechnology, vol. 38, no. 1, pp. 24–39, 2008. View at Publisher · View at Google Scholar · View at Scopus
  154. N. Jenkins, “Modifications of therapeutic proteins: challenges and prospects,” Cytotechnology, vol. 53, no. 1–3, pp. 121–125, 2007. View at Publisher · View at Google Scholar · View at Scopus
  155. G. Walsh and R. Jefferis, “Post-translational modifications in the context of therapeutic proteins,” Nature Biotechnology, vol. 24, no. 10, pp. 1241–1252, 2006. View at Publisher · View at Google Scholar · View at Scopus
  156. J. Ihssen, M. Kowarik, S. Dilettoso, C. Tanner, M. Wacker, and L. Thöny-Meyer, “Production of glycoprotein vaccines in Escherichia coli,” Microbial Cell Factories, vol. 9, article 61, 2010. View at Publisher · View at Google Scholar · View at Scopus
  157. M. Kowarik, S. Numao, M. F. Feldman et al., “N-linked glycosylation of folded proteins by the bacterial oligosaccharyltransferase,” Science, vol. 314, no. 5802, pp. 1148–1150, 2006. View at Publisher · View at Google Scholar · View at Scopus
  158. V. S. Terra, D. C. Mills, L. E. Yates, S. Abouelhadid, J. Cuccui, and B. W. Wren, “Recent developments in bacterial protein glycan coupling technology and glycoconjugate vaccine design,” Journal of Medical Microbiology, vol. 61, no. 7, pp. 919–926, 2012. View at Publisher · View at Google Scholar · View at Scopus
  159. M. Wacker, D. Linton, P. G. Hitchen et al., “N-linked glycosylation in Campylobacter jejuni and its functional transfer into E. coli,” Science, vol. 298, no. 5599, pp. 1790–1793, 2002. View at Publisher · View at Google Scholar · View at Scopus
  160. A. A. Ollis, S. Zhang, A. C. Fisher, and M. P. DeLisa, “Engineered oligosaccharyltransferases with greatly relaxed acceptor-site specificity,” Nature Chemical Biology, vol. 10, no. 10, pp. 816–822, 2014. View at Publisher · View at Google Scholar · View at Scopus
  161. J. D. Valderrama-Rincon, A. C. Fisher, J. H. Merritt et al., “An engineered eukaryotic protein glycosylation pathway in Escherichia coli,” Nature Chemical Biology, vol. 8, no. 5, pp. 434–436, 2012. View at Publisher · View at Google Scholar · View at Scopus
  162. J. Cuccui and B. Wren, “Hijacking bacterial glycosylation for the production of glycoconjugates, from vaccines to humanised glycoproteins,” The Journal of Pharmacy and Pharmacology, vol. 67, no. 3, pp. 338–350, 2015. View at Publisher · View at Google Scholar
  163. J. H. Merritt, A. A. Ollis, A. C. Fisher, and M. P. Delisa, “Glycans-by-design: engineering bacteria for the biosynthesis of complex glycans and glycoconjugates,” Biotechnology and Bioengineering, vol. 110, no. 6, pp. 1550–1564, 2013. View at Publisher · View at Google Scholar · View at Scopus
  164. M. Wetter, M. Kowarik, M. Steffen, P. Carranza, G. Corradin, and M. Wacker, “Engineering, conjugation, and immunogenicity assessment of Escherichia coli O121 O antigen for its potential use as a typhoid vaccine component,” Glycoconjugate Journal, vol. 30, no. 5, pp. 511–522, 2013. View at Publisher · View at Google Scholar · View at Scopus
  165. A. C. Fisher, C. H. Haitjema, C. Guarino et al., “Production of secretory and extracellular N-linked glycoproteins in Escherichia coli,” Applied and Environmental Microbiology, vol. 77, no. 3, pp. 871–881, 2011. View at Publisher · View at Google Scholar · View at Scopus