- About this Journal
- Abstracting and Indexing
- Aims and Scope
- Article Processing Charges
- Articles in Press
- Author Guidelines
- Bibliographic Information
- Citations to this Journal
- Contact Information
- Editorial Board
- Editorial Workflow
- Free eTOC Alerts
- Publication Ethics
- Reviewers Acknowledgment
- Submit a Manuscript
- Subscription Information
- Table of Contents
Infectious Diseases in Obstetrics and Gynecology
Volume 2011 (2011), Article ID 963513, 9 pages
Chlamydia trachomatis Vaccine Research through the Years
Department of Molecular Biotechnology, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000 Ghent, Belgium
Received 17 January 2011; Revised 13 April 2011; Accepted 2 May 2011
Academic Editor: J. Paavonen
Copyright © 2011 Katelijn Schautteet 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.
Chlamydia trachomatis is a Gram-negative obligate intracellular bacterium. It is the leading cause of bacterial sexual transmitted infections (STIs). World Health Organization figures estimated that over 90 million new cases of genital C. trachomatis infections occur worldwide each year. A vaccination program is considered to be the best approach to reduce the prevalence of C. trachomatis infections, as it would be much cheaper and have a greater impact on controlling C. trachomatis infections worldwide rather than a screening program or treating infections with antibiotics. Currently, there are no vaccines available which effectively protect against a C. trachomatis genital infection despite the many efforts that have been made throughout the years. In this paper, the many attempts to develop a protective vaccine against a genital C. trachomatis infection will be reviewed.
Chlamydia trachomatis is a Gram-negative obligate intracellular bacterium. It is the leading cause of bacterial sexually transmitted disease in both developed and developing countries with more than 90 million new cases of genital C. trachomatis infections occurring each year . In the past years, an increase in the number of STIs and in particular of C. trachomatis infections has been observed in many, if not all, European countries . This increase might be attributed to changes in attitudes, increased awareness of healthcare workers, and improved diagnostics.
In the genital tract, infection with C. trachomatis is propagated within the single cell columnar layer of the epithelium in the urethra of men and the endocervix of women. Within the epithelial cells, C. trachomatis undergoes a unique biphasic developmental cycle consisting of an infectious, but metabolically inert, elementary body (EB) and a noninfectious, but metabolically active, reticulate body (RB). After completion of the developmental cycle, the EBs are released and infect neighboring epithelial cells, thereby spreading the infection.
Infection can result in acute inflammation characterized by redness, edema, and mucosal discharge and is diagnosed clinically as mucopurulent cervicitis in women and non-gonococcal urethritis in men [3, 4]. In women, infection can manifest as abnormal vaginal discharge and/or postcoital bleeding, while the infection is limited to the lower genital tract and irregular uterine bleeding and/or pelvic discomfort once the infection ascends to the upper genital tract . Symptoms in males are generally limited to dysuria and moderate clear to whitish discharge . While these symptoms signify an infection, the absence of such symptoms does not necessarily indicate the absence of infection. Up to 75% of women and 50% of men infected with C. trachomatis are asymptomatic [5, 6], and these infected people do not seek medical attention. If the infection remains untreated, it often results in pelvic inflammatory disease (PID), tubal scarring, ectopic pregnancy, and chronic pelvic pain in women which could lead to infertility, epididymitis in men, and infant pneumonia in children [7–10].
Although very effective antimicrobial therapy is available, a vaccination program is considered to be the best approach to reduce the prevalence of C. trachomatis infections. It would be much cheaper and have a greater impact on controlling C. trachomatis infections worldwide than a screening program or treating infections with antibiotics. Long-term induced immunity against STIs such as C. trachomatis would be preferable. However, since STIs have the highest incidence at the reproductive age, even short- to medium-term immunity would be of great benefit. Therefore, a C. trachomatis vaccine protecting at least women in their fertile period against complications would be a valuable tool in achieving a higher level of public health. Currently, there are no vaccines available against a C. trachomatis genital infection despite the many efforts that have been made throughout the years to develop a protective C. trachomatis vaccine. In this paper the many attempts to develop a protective vaccine against a genital C. trachomatis infection will be reviewed.
2. Chlamydia muridarum versus C. trachomatis Mouse Models
The most used animal model to study C. trachomatis female tract infections is the mouse model. The mouse is susceptible to C. muridarum mouse pneumonitis (MoPn), formerly known as the mouse biovar of C. trachomatis, and to human genital tract isolates of C. trachomatis. The genomes of these species share remarkable similarities in the content and order of genes and in the presence of putative virulence factors . An important difference between the species is the absence and presence of a tryptophan operon in the genome of C. trachomatis and C. muridarum, respectively [12, 13]. Consequently, these biovars have differential sensitivity to IFN-γ, a cytokine which plays an important role in the early clearance of chlamydia from the genital tract . Most likely the C. muridarum and the C. trachomatis strain will also differ in response to other cytokines.
There are also significant differences in virulence characteristics among both biovars. In contrast to human isolates, C. muridarum is able to cause severe upper genital tract pathology and a high incidence of infertility after a single infection in mice . In addition, the developmental cycle of C. muridarum is more rapid, its duration being approximately half that of human strains, and the strain is more prolific. Chlamydia muridarum can infect mice of various strains nearly equally, while infection of mice with C. trachomatis is highly dependable on the mouse strain. Overall, lower shedding and minimal to moderate inflammation can be noticed in mice infected with C. trachomatis. Furthermore, postinfection sequelae are less common. This is in accordance to the fact that upper genital tract progression followed by pathology, usually resulting from multiple infections, is only seen in a small percentage of women .
In contrast to C. muridarum infection, C. trachomatis infection was unaltered in the absence of CD4+ T cells. Mice infected with C. trachomatis developed protective immunity to rechallenge, but unlike C. muridarum infection, optimum resistance required multiple infectious challenges despite the generation of adaptive serum and local chlamydial specific immune responses. Thus, understanding the chlamydial pathogenic and host immunologic factors that result in a diminished protective role for CD4+ T cells in C. trachomatis murine infection might lead to new insights important to human immunity and vaccine development . It has been demonstrated that strong adaptive immune responses are generated when mice are infected with C. trachomatis serovars [3, 18, 19], but it has also been shown that these infections in mice can resolve in the absence of adaptive immunity, suggesting that innate immune responses alone can resolve infection . This is not necessarily a reason to invalidate the use of C. trachomatis serovars in murine studies of genital tract infection or in vaccine development. It could be that the rather mild infection seen in murine studies utilizing human C. trachomatis biovars may replicate some aspects of human infection. In order to resolve the murine C. muridarum genital infection and to protect against reinfection, adaptive immune responses are absolutely indispensable.
As there are considerable differences between the C. muridarum and the C. trachomatis murine model, it is difficult to make direct comparisons. In order to understand the pathogenesis of human chlamydial infections completely, it is absolutely necessary to thoroughly investigate chlamydial infection in its natural human host .
3. Protective Immune Responses to C. trachomatis
Information on the immune mechanisms of clearance of infection and resistance to reinfection has been provided in particular by mouse models of genital infection. T cells, especially major histocompatibility complex (MHC) class II-restricted CD4+ T cells, are required for protective immunity [21–24]. MHC class I-restricted CD8+ T cells, on the other hand, are not necessary for infection resolution or immunity to reinfection [21–24]. The protective role of antibody is less easily discernible than that of the cellular response, but important to vaccine development, it is as protective as CD4+ T cells in immunity to reinfection [22, 25]. Furthermore, Th1 cytokines, specifically IFN-γ and interleukin-12 (IL-12), are essential to induce a protective response [13, 26, 27]. In women, CD4+ T cells are indeed recruited to the cervix during active infection; however, CD8+ and dentritic cells are also recruited, and the relative proportions of these cells may be situational. Different studies involving women have confirmed that local Th1 cytokines, mainly IFN-γ, are associated with C. trachomatis infection (reviewed by ) although these studies have not been able to determine which specific responses lead to infection resolution versus persistence [29–31]. Serum and genital mucosal IgG and IgA antibodies to specific C. trachomatis proteins and to chlamydial EBs are usually detected during active infection in women [32–34]. These antibody responses in humans infected with C. trachomatis, including those measured in endocervical secretions, have not been found to correlate with protective immunity but appear to be markers of prior infection.
When developing a vaccine against genital C. trachomatis infections, it is important to take into account the unique properties of the genital tract. This mucosal site is unique among mucosal effector tissues, as it lacks organized lymphatics which can result in a delayed systemic response relative to other sites . Furthermore, the female genital tract is also subjected to hormonal regulation, and the effectiveness of intravaginal vaccination has been shown to be influenced by the phase of the menstrual cycle [35–37]. The immunological characteristics of the genital tract and the tropism of chlamydia for mucosal epithelial cells show that a C. trachomatis vaccine has to induce both mucosal and systemic protective responses.
4. Whole Organism Vaccines—First-Generation C. trachomatis Vaccines
Initial attempts to develop an effective vaccine for controlling both animal and human chlamydial infections began with the use of inactivated or live, attenuated whole organism preparations in the 1950s. These vaccines can offer a degree of protection but are far from ideal. Common problems are the cost and the complexity of production, the requirement for cold storage, the presence of antigens which can induce autoimmunity or immunopathology, and the limited efficacy in neonates with high levels of maternal antibodies .
4.1. Live Attenuated Organisms
The first vaccines that were used against Chlamydiaceae were live vaccines. With this method of immunization, attenuated or modified living chlamydial organisms were used. The development of attenuated strains usually happens by a number of passages of the wild-type strain in different types of cell cultures or by chemical mutagenesis. Due to the passages, one or more mutations could arise, resulting in a nonvirulent attenuated strain. Live attenuated vaccines can elicit humoral and cellular immunity, because they replicate in a manner analogous to the target pathogen, promoting the processing and presentation of antigens in a way that is most similar to the natural infection . On the other hand, they can also revert to the virulent wild-type strain resulting in disease or persistent infection. Whole-organism vaccination is unlikely to be attempted in the near future, because there is a risk of immunopathology, the large-scale production of pure chlamydiae is extremely difficult  and because of the possible spread of live Chlamydiaceae in the environment .
In the 1960s, unsuccessful vaccination trials with live attenuated vaccines against trachoma were performed in humans and primates . Four decades later, several authors have explored the possibility to vaccinate with live attenuated bacteria against genital C. trachomatis infection.
Peterson et al.  immunized mice intranasally or intraperitoneally with viable C. trachomatis, serovar E. Mice immunized intranasally with live C. trachomatis exhibited significant protection upon a vaginal infection, while intraperitoneally immunized mice did not. However, the protection was not complete. Su et al.  performed an experiment in mice to investigate the ability of a live attenuated C. trachomatis vaccine to prevent genital infection. Mice were treated with a subchlamydiacidal concentration of oxytetracycline following vaginal infection. Results showed that a self-limiting subclinical infection of the murine genital tract with C. trachomatis is as efficient as a clinically apparent acute infection in generating a protective anti-chlamydial immune response. Based on these results, the authors concluded that a live attenuated vaccine would be useful for the prevention of chlamydial STIs. Recently, Olivares-Zavaleta et al.  evaluated the protective immunity of the attenuated C. trachomatis L2 (25667R) strain in a murine model. They concluded that intravaginal vaccination with the live-attenuated strain L2 is safe, induces a systemic antibody and a CD4+ Th1-based immune response, but its protective efficacy is limited to reducing chlamydial burden at early time periods after-infection.
Recently, Yu et al.  vaccinated mice intranasally with live C. muridarum with or without CpG-containing oligodeoxynucleotide 1862. Immunization elicited widely disparate levels of protective immunity to genital tract challenge. Protection was correlated with the frequency of multifunctional T cells coexpressing IFN-γ and TNF-α with or without IL-2. These results suggest that IFN-γ producing CD4+ T cells that highly coexpress TNF- α may be the optimal effector cells for protective immunity.
In view of the safety aspects (possible return to the virulent wild type strain) and the risk for immunopathological damage, it seems unlikely that a live attenuated C. trachomatis vaccine will be allowed in humans.
4.2. Inactivated or Killed Organisms
Because live vaccines are not always safe or available, research switched to the use of killed or inactivated organisms. Inactivation was done by heat or chemical treatment. Compared to live organisms, inactivated or killed vaccines also have some disadvantages. They may contain undesirable components like bacterial endotoxins, that can cause detrimental side effects, or nonprotective components that may reduce the degree of protection that is required. Their major disadvantage is that they are not able to replicate anymore, which stresses the need to revaccinate and to use adjuvants. Another consequence of their inability to replicate is that they are poor inducers of cell-mediated immunity although they can induce and adequate level of humoral immunity . Because a strong cell-mediated immunity is needed for clearance of chlamydial infections, inactivated or killed organisms seem to be less suitable for vaccine development against Chlamydiaceae.
Studies on inactivated or killed organism vaccines against genital C. trachomatis infection are rare. In this study, Peterson et al.  failed to elicit a protective response to a vaginal C. trachomatis infection in mice immunized intranasally and intraperitoneally with 1 × 106 UV inactivated inclusion forming units of C. trachomatis serovar E.
5. Subunit Vaccines—Second-Generation C. trachomatis Vaccines
In order to avoid harmful effect of the preparations containing the whole organism, it was proposed that a subunit vaccine was needed. Subunit vaccines are safer, they cannot revert to a virulent form, and undesirable antigens, which can induce immunopathology or inflammatory damage, can be avoided . Vaccine candidate antigens, or parts of antigens, may be represented as purified proteins, recombinant proteins or as synthetic proteins . But subunit vaccines have also some disadvantages. Like inactivated vaccines, they are poor inducers of cell-mediated immunity , which is very important in the defense against chlamydial infections. Furthermore, the use of adjuvants is being recommended.
5.1. Purified MOMP and COMC Preparations
Following the identification of the major outer membrane protein (MOMP) as the structurally and immunologically dominant protein in the chlamydial outer membrane , vaccine research mainly focused on this protein. Some results were encouraging while others rather disappointing. Pal et al.  found that a chlamydial outer membrane complex (COMC) preparation of C. muridarum could induce significantly protective immunity in mice against a genital challenge, while purified MOMP preparations could not. Some years later, the same research group immunized mice with a purified and refolded preparation of the C. muridarum MOMP in combination with Freund’s adjuvants. A significant level of protection was conferred in the vaccinated mice against a genital challenge . Cheng et al.  demonstrated the protective potential of native MOMP of a C. muridarum serovar in combination with novel adjuvants, the nontoxic subunit B of cholera toxin (CTB-CpG). Immunization elicited a significant antigen-specific antibody and cell-mediated immune response as well as protection against a pulmonary challenge with C. muridarum. Cunningham et al.  could demonstrate that immunization of mice with purified C. muridarum MOMP could induce neutralizing antibodies which leaded to reduced numbers of infected mice. Surprisingly, these antibodies also accelerated the development of severe oviduct pathology. Therefore, it is important to keep in mind that immunity can potentially induce pathology and this should be considered when designing vaccines.
Igietseme and Murdin  prepared a MOMP-ISCOM vaccine based on MOMP extracted from C. trachomatis serovar D. This vaccine was able to produce a Th1 antigen-specific immune response, and immunized mice cleared a vaginal infection within one week.
From these studies, it is clear that some preparations can induce more protection than others. This is probably due to the difference in extraction method which can influence the preservation of conformational MOMP epitopes, necessary for protection. Although vaccination with refolded, purified MOMP preparations have been reasonable successful, the major drawbacks of these vaccines are that they are very expensive and there are problems to grow chlamydia in bulk, which renders these kinds of vaccines commercially non-viable .
5.2. Recombinant Proteins
Nowadays, it is possible to produce high amounts of bacterial proteins by recombinant DNA technology which is cheaper and more cost effective. The genes, coding for protective antigens, will be expressed in prokaryotic or eukaryotic cells that will produce the desired recombinant protein. For chlamydial vaccines, recombinant MOMP (rMOMP) is generally used. However, the expression of full-length rMOMP in prokaryotic expression systems is generally toxic, and it is also difficult to produce rMOMP in a native form with intact, conformationally relevant epitopes . Moreover, the chlamydial MOMP is glycosylated [56, 57].
Different attempts were made to elicit protection against a C. trachomatis infection by rMOMP vaccination. Transcutaneous immunization with MOMP in combination with the cholera toxin and CpG oligodeoxynucleotides elicits IgG and IgA antibody response in the vaginal and cervical lavage fluid and an IgG antibody response in the serum. Furthermore, IFN-γ secreting T cells were activated in the draining lymph nodes. The immunization protocol resulted in enhanced clearance of C. muridarum following intravaginal challenge of mice . Pal et al.  demonstrated that immunisation with purified C. muridarum MOMP, co-administered with Borrelia burgdorferi Outer surface protein (Osp) A as adjuvant, can induce significant protection in mice against a C. muridarum genital infection. Sun et al.  compared vaccines based on recombinant (rMOMP) and native MOMP (nMOMP). The recombinant preparation based on C. muridarum MOMP can elicit a protective immune response in mice against an intranasal challenge. However, the degree of protection obtained with the rMOMP was not as robust as that achieved with an nMOMP preparation indicating that the structural conformation of the MOMP is important for inducing protection. Hickey et al.  showed that transcutaneous immunization of mice with rMOMP incorporated in lipid C, induces partial protection of both the respiratory and genital mucosae against challenge with C. muridarum. The efficacy of a recombinant vaccine is not only defined by the protein that is used but also by the administration routes. It has been proven that a combined systemic and mucosal vaccination with rMOMP provides better protection against a challenge with C. muridarum than either systemic or mucosal immunization alone . Systemic immunization of mice with rMOMP from C. trachomatis could reduce the number of animals developing severe salpingitis but failed to reduce chlamydial colonization of the lower genital tract. Mice, immunized with rMOMP directly into the Peyer’s patches (to stimulate mucosal immunity), shed fewer chlamydiae from the vagina, but showed little reduction in oviduct damage. Furthermore, the number of animals developing severe salpingitis could not be reduced. Although in both cases specific IgG and IgA antibody responses could be observed, they could not completely protect the mice .
Although most recombinant vaccines are based on MOMP, other proteins can also be viable vaccine candidates. In 2007, a novel vaccination strategy using a secreted protein, chlamydial protease-like activity factor (CPAF) was developed by Murthy et al. . Intranasal immunization using recombinant CPAF (rCPAF) accompanied by interleukin-12 (IL-12) was used to assess the protective immunity against genital C. muridarum infection in BALB/c mice. rCPAF + IL-12-vaccinated mice displayed significantly reduced bacterial shedding upon chlamydial challenge and accelerated resolution of infection compared to mock-immunized animals. Moreover, rCPAF + IL-12-immunized animals exhibited protection against pathological consequences of chlamydial infection. These results demonstrate for the first time that a secreted chlamydial protein, CPAF, is a viable vaccine candidate that should be considered for induction of efficacious, antichlamydial immunity. The chlamydial proteins OmcB and rl16 have been identified as human B and T cell targets during chlamydial infections in humans [65, 66]. Vaccination of mice with a fusion protein (CTH1) composed of those two antigens promoted a CD4+ T-cell dependent protective response but lacks a CD4 independent protective mechanism for complete protection .
5.3. Synthetic Peptides
Today, computer-based methods to predict antigenic domains or epitopes are available. Synthetic production of these epitopes makes it possible to produce synthetic peptides which correspond with the important immunogenic domains on the antigens. On the other hand, we have to take into account that a lot of antigenic determinants need conformational or three-dimensional structures, like in the complete protein, to elicit an immune response.
Studies with MOMP peptides and oligopeptide vaccines showed variable results with maximum partial protection. Preliminary studies in mice indicated that intradermal injection of a peptide from a conserved region of the MOMP of C. trachomatis, conferred some protection against the development of salpingitis . In contrast to these findings, Su et al.  found that parenteral immunization of mice with an alum-adsorbed synthetic oligopeptide of the C. trachomatis MOMP, was ineffective in preventing chlamydial genital tract infection although mice produced high levels of antichlamydial serum IgG neutralizing antibodies. Therefore, DNA vaccination which induces both humoral and cellular immune responses can be an alternative method to protect animals from chlamydial infections.
6. DNA Vaccines—Third-Generation C. trachomatis Vaccines
DNA immunization represents a novel approach to vaccine and immunotherapeutic development. Injection of plasmid DNA encoding a foreign gene of interest can result in the subsequent expression of the foreign gene product and the induction of an immune response within the host. DNA vaccines have a number of advantages when compared with alternative vaccination strategies . They encode multiple immunogenic epitopes and evoke both humoral and cell-mediated immune responses. The immunogenic epitopes are presented to the immune system in their native form. Therefore, DNA vaccines exhibit the advantages of attenuated vaccines without the safety problems associated with the in vivo replication and possible reversion to a virulent form. Due to the endogenous production of the antigen, a more balanced Th1/Th2 like immune response is elicited . Plasmid vectors can be rapidly constructed and easily tested. Large-scale manufacturing procedures are available and the DNA can be easily and inexpensively purified to homogeneity, resulting in lower costs to develop and manufacture this type of vaccine [42, 72]. This makes this strategy applicable as a human vaccine approach in underdeveloped countries and as a veterinary vaccine strategy, where the cost per dose is of major economic concern. In addition, DNA is more thermostable than vaccine strategies which require a cold chain for storage , and it should exhibit a longer shelf-life because of the improved stability. The production of combination vaccines employing DNA is also simplified. DNA also allows a more simplified and effective quality control process that provides additional cost benefits.
In addition, there are some concerns and potential disadvantages of DNA vaccines. Firstly, the DNA could possibly integrate into the host chromosome. This has not been proven yet, and it is thought that the chance that this will happen is lower than the spontaneous mutation frequency . A second concern of DNA vaccination is the possibility of generating antibodies to DNA. Immune responses to DNA occur in autoimmune diseases, and the possibility exists that bacterial DNA injection could induce an immune response that might cross-react with host DNA . Thirdly, long-term expression of injected DNA into muscle cells may have an effect on immune responses to subsequent vaccination with different DNA, and the immune responses to protective epitopes associated with this second immunization can be compromised. The fourth disadvantage is that DNA vaccination strategies are unsuccessful when evaluating non-protein-based antigens, such as bacterial polysaccharides and lipids . Other possible disadvantages are the low transfection and expression efficiency of DNA vaccines, certainly in large animals and humans . However, by using various combinations of delivery systems and different adjuvants, the immune response can be enhanced. In the past, different studies have evaluated the protective potential of DNA vaccines against chlamydial infections.
6.1. C. trachomatis DNA Vaccination
The first attempt to generate an MOMP-based DNA vaccine against a genital chlamydial challenge was disappointing . This vaccine encoded the MOMP gene of C. muridarum. Only modest immune response was elicited, but no protection could be established against infection or disease. Because DNA immunization alone did not generate immune responses or protection to the same extent as those induced by using live organisms, combinational vaccines were evaluated. DNA priming followed by boosting with immune-stimulating complexes (ISCOM) of MOMP protein (MOMP ISCOM) in mice resulted in higher protection when compared to mice given MOMP ISCOM immunization alone . In 2010 and 2011, Schautteet et al. [78, 79] studied the ability of a DNA vaccine based on C. trachomatis MOMP to protect against genital C. trachomatis infection in a recently developed pig model . When administrating the vaccine to the vaginal mucosa, a cellular immune response was induced which elicited significant protection in pigs. The infection could not be cleared completely . When the DNA vaccine was administered combined to the nasal and vaginal mucosa of the pig, both cellular and humoral immune responses were induced which contributed to the significant protection of pigs against a genital C. trachomatis infection .
Since a couple of years, other genes than ompA were evaluated for their potential as vaccine candidates. DNA immunization with the pgp3 gene of C. trachomatis could inhibit the spread of the infection from the lower to the upper genital tract . The pgp3 gene encodes a 28 kDa polypeptide found on the pCT plasmid of C. trachomatis which may provide a function related to chlamydial cell physiology . Ifere et al.  developed a DNA vaccine composed of MOMP and the porin B protein (PorB) of C. trachomatis. A recombinant Vibrio Cholerae ghost (rVCG) was used as carrier and delivery system. Significant higher levels of Th1 response and secretory IgA and IgG2a were induced by immunization. Furthermore, all animals which were immunized with the multisubunit vaccine completely resolved the infection two weeks after challenge. In 2008, a pORF5 DNA vaccine was evaluated for its protective immunity in a mouse model of genital chlamydial infection. The vaccinated mice displayed significantly reduced bacterial shedding upon chlamydial challenge and an accelerated resolution of the infection. Furthermore, the immunized mice also exhibited protection against pathological consequences of chlamydial infection. These results demonstrate the potential of the pORF5 DNA vaccine to elicit protective immunity against a genital chlamydial challenge .
7. Impact of a C. trachomatis Vaccine
Recently, a mathematical model has been developed that simulates transmission in a heterosexual population by linking the within-host biology of susceptibility and the chlamydia-infected individuals to their sexual behavior and partnership dynamics . The model tracks the infection time course, disease progression, and dynamic infectiousness of infected individuals and the transmission to others. The authors have demonstrated that if a fully protective vaccine is available, and this will be administered to adolescents before their sexual debut, epidemics of chlamydia infection could be eradicated within 20 years. Furthermore, it is likely that targeting 100% of one sex (females) will have a greater epidemiological impact than administering vaccines to 50% of both sexes. If lifelong sterilizing immunity cannot be achieved, a chlamydia vaccine should be effective for at least 10 years in order to lead to population-level eradication. Based on the information generated by this mathematical model, the candidate vaccines should protect individuals by raising the infectiousness threshold and secondary reduce the peak load and the duration of the infection in vaccinated individuals who become infected.
Vaccination could be substantially more effective than other biomedical interventions in controlling epidemics of chlamydia infection. Currently, the best public health intervention available is increasing the rate of screening and treating infected individuals. Administrating a protective vaccine to adolescents before their first sexual experience could induce a significant reduction in prevalence which could not be obtained by screening teenagers, even with a coverage of 100% . Unfortunately, no protective vaccines, either fully or partially, are available although there have been many attempts to develop one. The reasons for the variability in success are still unclear but are probably a consequence of different immunization protocols and a reflection of the different protective mechanisms required for the different infections .
- WHO, Global Prevalence and Incidence of Selected Sexually Transmitted Diseases: Overviews and Estimates, World Health Organization, Geneva, Switzerland, 1996.
- C. Bébéar and B. de Barbeyrac, “Genital Chlamydia trachomatis infections,” Clinical Microbiology and Infection, vol. 15, no. 1, pp. 4–10, 2009.
- R. C. Brunham and J. Rey-Ladino, “Immunology of Chlamydia infection: implications for a Chlamydia trachomatis vaccine,” Nature Reviews Immunology, vol. 5, no. 2, pp. 149–161, 2005.
- J. F. Peipert, “Genital chlamydial infections,” New England Journal of Medicine, vol. 349, no. 25, pp. 2424–2430, 2003.
- G. F. Gonzales, G. Muñoz, R. Sánchez et al., “Update on the impact of Chlamydia trachomatis infection on male fertility,” Andrologia, vol. 36, no. 1, pp. 1–23, 2004.
- W. E. Stamm, “Chlamydia trachomatis infections: progress and problems,” Journal of Infectious Diseases, vol. 179, no. 2, pp. S380–383, 1999.
- A. I. A. Ibrahim, A. Refeidi, and A. A. El Mekki, “Etiology and clinical features of acute epididymo-orchitis,” Annals of Saudi Medicine, vol. 16, no. 2, pp. 171–174, 1996.
- D. Taylor-Robinson and B. J. Thomas, “The role of Chlamydia trachomatis in genital-tract and associated diseases,” Journal of Clinical Pathology, vol. 33, no. 3, pp. 205–233, 1980.
- A. E. Washington and P. Katz, “Cost of and payment source for pelvic inflammatory disease: trends and projections, 1983 through 2000,” Journal of the American Medical Association, vol. 266, no. 18, pp. 2565–2569, 1991.
- L. Westrom, R. Joesoef, G. Reynolds, A. Hagdu, and S. E. Thompson, “Pelvic inflammatory disease and fertility: a cohort study of 1,844 women with laparoscopically verified disease and 657 control women with normal laparoscopic results,” Sexually Transmitted Diseases, vol. 19, no. 4, pp. 185–192, 1992.
- R. J. Belland, M. A. Scidmore, D. D. Crane et al., “Chlamydia trachomatis cytotoxicity associated with complete and partial cytotoxin genes,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 24, pp. 13984–13989, 2001.
- D. E. Nelson, D. P. Virok, H. Wood et al., “Chlamydial IFN-γ immune evasion is linked to host infection tropism,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 30, pp. 10658–10663, 2005.
- L. L. Perry, H. Su, K. Feilzer et al., “Differential sensitivity of distinct Chlamydia trachomatis isolates to IFN-γ-mediated inhibition,” Journal of Immunology, vol. 162, no. 6, pp. 3541–3548, 1999.
- M. Johansson, K. Schön, M. Ward, and N. Lycke, “Genital tract infection with Chlamydia trachomatis fails to induce protective immunity in gamma interferon receptor-deficient mice despite a strong local immunoglobulin a response,” Infection and Immunity, vol. 65, no. 3, pp. 1032–1044, 1997.
- J. M. Lyons, J. I. Ito, A. S. Peña, and S. A. Morré, “Differences in growth characteristics and elementary body associated cytotoxicity between Chlamydia trachomatis oculogenital serovars D and H and Chlamydia muridarum,” Journal of Clinical Pathology, vol. 58, no. 4, pp. 397–401, 2005.
- I. G. M. van Valkengoed, S. A. Morré, A. J. C. van den Brule, C. J. L. M. Meijer, L. M. Bouter, and A. J. P. Boeke, “Overestimation of complication rates in evaluations of Chlamydia trachomatis screening programmes—implications for cost-effectiveness analyses,” International Journal of Epidemiology, vol. 33, no. 2, pp. 416–425, 2004.
- S. G. Morrison, C. M. Farris, G. L. Sturdevant, W. M. Whitmire, and R. P. Morrison, “Murine Chlamydia trachomatis genital infection is unaltered by depletion of CD4+ T cells and diminished adaptive immunity,” Journal of Infectious Diseases, vol. 203, no. 8, pp. 1120–1128, 2011.
- R. C. Brunham, D. J. Zhang, X. Yang, and G. M. McClarty, “The potential for vaccine development against chlamydial infection and disease,” Journal of Infectious Diseases, vol. 181, no. 6, pp. S538–S543, 2000.
- L. Hafner, K. Beagley, and P. Timms, “Chlamydia trachomatis infection: host immune responses and potential vaccines,” Mucosal Immunology, vol. 1, no. 2, pp. 116–130, 2008.
- S. A. Morré, J. M. Lyons, J. Ito, and R. P. Morrison, “Murine models of Chlamydia trachomatis genital tract infection: use of mouse pneumonitis strain versus human strains,” Infection and Immunity, vol. 68, no. 12, pp. 7209–7211, 2000.
- R. P. Morrison, K. Feilzer, and D. B. Tumas, “Gene knockout mice establish a primary protective role for major histocompatibility complex class II-restricted responses in Chlamydia trachomatis genital tract infection,” Infection and Immunity, vol. 63, no. 12, pp. 4661–4668, 1995.
- S. G. Morrison, H. Su, H. D. Caldwell, and R. P. Morrison, “Immunity to murine Chlamydia trachomatis genital tract reinfection involves B cells and CD4(+) T cells but not CD8(+) T cells,” Infection and Immunity, vol. 68, no. 12, pp. 6979–6987, 2000.
- S. G. Morrison and R. P. Morrison, “Resolution of secondary Chlamydia trachomatis genital tract infection in immune mice with depletion of both CD4(+) and CD8(+) T cells,” Infection and Immunity, vol. 69, no. 4, pp. 2643–2649, 2001.
- H. Su and H. D. Caldwell, “CD4(+) T cells play a significant role in adoptive immunity to Chlamydia trachomatis infection of the mouse genital tract,” Infection and Immunity, vol. 63, no. 9, pp. 3302–3308, 1995.
- S. G. Morrison and R. P. Morrison, “A predominant role for antibody in acquired immunity to chlamydial genital tract reinfection,” Journal of Immunology, vol. 175, no. 11, pp. 7536–7542, 2005.
- T. W. Cotter, K. H. Ramsey, G. S. Miranpuri, C. E. Poulsen, and G. I. Byrne, “Dissemination of Chlamydia trachomatis chronic genital tract infection in gamma interferon gene knockout mice,” Infection and Immunity, vol. 65, no. 6, pp. 2145–2152, 1997.
- L. L. Perry, K. Feilzer, and H. D. Caldwell, “Immunity to Chlamydia trachomatis is mediated by T helper 1 cells through IFN-γ-dependent and -independent pathways,” Journal of Immunology, vol. 158, no. 7, pp. 3344–3352, 1997.
- B. E. Batteiger, F. Xu, R. E. Johnson, and M. L. Rekart, “Protective immunity to Chlamydia trachomatis genital infection: evidence from human studies,” Journal of Infectious Diseases, vol. 201, supplement 2, pp. S178–S189, 2010.
- T. Agrawal, V. Vats, P. K. Wallace, S. Salhan, and A. Mittal, “Cervical cytokine responses in women with primary or recurrent chlamydial infection,” Journal of Interferon and Cytokine Research, vol. 27, no. 3, pp. 221–226, 2007.
- J. N. Arno, V. A. Ricker, B. E. Batteiger, B. P. Katz, V. A. Caine, and R. B. Jones, “Interferon-γ in endocervical secretions of women infected with Chlamydia trachomatis,” Journal of Infectious Diseases, vol. 162, no. 6, pp. 1385–1389, 1990.
- W. M. Geisler, “Duration of untreated, uncomplicated Chlamydia trachomatis genital infection and factors associated with chlamydia resolution: a review of human studies,” Journal of Infectious Diseases, vol. 201, supplement 2, pp. S104–S113, 2010.
- T. Agrawal, V. Vats, S. Salhan, and A. Mittal, “Mucosal and peripheral immune responses to chlamydial heat shock proteins in women infected with Chlamydia trachomatis,” Clinical and Experimental Immunology, vol. 148, no. 3, pp. 461–468, 2007.
- S. Ghaem-Maghami, G. Ratti, M. Ghaem-Maghami et al., “Mucosal and systemic immune responses to plasmid protein pgp3 in patients with genital and ocular Chlamydia trachomatis infection,” Clinical and Experimental Immunology, vol. 132, no. 3, pp. 436–442, 2003.
- M. S. Pate, S. R. Hedges, D. A. Sibley, M. W. Russell, E. W. Hook, and J. Mestecky, “Urethral cytokine and immune responses in Chlamydia trachomatis-infected males,” Infection and Immunity, vol. 69, no. 11, pp. 7178–7181, 2001.
- J. Mestecky, Z. Moldoveanu, and M. W. Russell, “Immunologic uniqueness of the genital tract: challenge for vaccine development,” American Journal of Reproductive Immunology, vol. 53, no. 5, pp. 208–214, 2005.
- E. L. Johansson, L. Wassén, J. Holmgren, M. Jertborn, and A. Rudin, “Nasal and vaginal vaccinations have differential effects on antibody responses in vaginal and cervical secretions in humans,” Infection and Immunity, vol. 69, no. 12, pp. 7481–7486, 2001.
- P. A. Kozlowski, S. B. Williams, R. M. Lynch et al., “Differential induction of mucosal and systemic antibody responses in women after nasal, rectal, or vaginal immunization: influence of the menstrual cycle,” Journal of Immunology, vol. 169, no. 1, pp. 566–574, 2002.
- S. Van Drunen Littel-Van Den Hurk, V. Gerdts, B. I. Loehr et al., “Recent advances in the use of DNA vaccines for the treatment of diseases of farmed animals,” Advanced Drug Delivery Reviews, vol. 43, no. 1, pp. 13–28, 2000.
- R. C. Brunham, D. J. Zhang, X. Yang, and G. M. McClarty, “The potential for vaccine development against chlamydial infection and disease,” Journal of Infectious Diseases, vol. 181, no. 6, supplement 3, pp. S538–S543, 2000.
- A. J. Stagg, “Vaccines against Chlamydia: approaches and progress,” Molecular Medicine Today, vol. 4, no. 4, pp. 166–173, 1998.
- P. E. Shewen, R. C. Povey, and M. R. Wilson, “A comparison of the efficacy of a live and four inactivated vaccine preparations for the protection of cats against experimental challenge with Chlamydia psittaci,” Canadian Journal of Comparative Medicine, vol. 44, no. 3, pp. 244–251, 1980.
- D. Longbottom and M. Livingstone, “Vaccination against chlamydial infections of man and animals,” Veterinary Journal, vol. 171, no. 2, pp. 263–275, 2006.
- E. M. Peterson, J. Z. You, V. Motin, and L. M. De La Maza, “Intranasal immunization with Chlamydia trachomatis, serovar E, protects from a subsequent vaginal challenge with the homologous serovar,” Vaccine, vol. 17, no. 22, pp. 2901–2907, 1999.
- H. Su, R. Messer, W. Whitmire, S. Hughes, and H. D. Caldwell, “Subclinical chlamydial infection of the female mouse genital tract generates a potent protective immune response: implications for development of live attenuated chlamydial vaccine strains,” Infection and Immunity, vol. 68, no. 1, pp. 192–196, 2000.
- N. Olivares-Zavaleta, W. Whitmire, D. Gardner, and H. D. Caldwell, “Immunization with the attenuated plasmidless Chlamydia trachomatis L2(25667R) strain provides partial protection in a murine model of female genitourinary tract infection,” Vaccine, vol. 28, no. 6, pp. 1454–1462, 2010.
- H. Yu, K. P. Karunakaran, I. Kelly et al., “Immunization with live and dead Chlamydia muridarum induces different levels of protective immunity in a murine genital tract model: correlation with MHC class II peptide presentation and multifunctional Th1 cells,” Journal of Immunology, vol. 186, no. 6, pp. 3615–3621, 2011.
- C. Olive, I. Toth, and D. Jackson, “Technological advances in antigen delivery and synthetic peptide vaccine developmental strategies,” Mini Reviews in Medicinal Chemistry, vol. 1, no. 4, pp. 429–438, 2001.
- J. Hess, U. Schaible, B. Raupach, and S. H. E. Kaufmann, “Exploiting the immune system: toward new vaccines against intracellular bacteria,” Advances in Immunology, vol. 75, pp. 1–88, 2000.
- H. D. Caldwell, J. Kromhout, and J. Schachter, “Purification and partial characterization of the major outer membrane protein of Chlamydia trachomatis,” Infection and Immunity, vol. 31, no. 3, pp. 1161–1176, 1981.
- S. Pal, I. Theodor, E. M. Peterson, and L. M. De la Maza, “Immunization with an acellular vaccine consisting of the outer membrane complex of Chlamydia trachomatis induces protection against a genital challenge,” Infection and Immunity, vol. 65, no. 8, pp. 3361–3369, 1997.
- S. Pal, I. Theodor, E. M. Peterson, and L. M. De la Maza, “Immunization with the Chlamydia trachomatis mouse pneumonitis major outer membrane protein can elicit a protective immune response against a genital challenge,” Infection and Immunity, vol. 69, no. 10, pp. 6240–6247, 2001.
- C. Cheng, I. Bettahi, M. I. Cruz-Fisher et al., “Induction of protective immunity by vaccination against Chlamydia trachomatis using the major outer membrane protein adjuvanted with CpG oligodeoxynucleotide coupled to the nontoxic B subunit of cholera toxin,” Vaccine, vol. 27, no. 44, pp. 6239–6246, 2009.
- K. A. Cunningham, A. J. Carey, L. Hafner, P. Timms, and K. W. Beagley, “Chlamydia muridarum major outer membrane protein-specific antibodies inhibit in vitro infection but enhance pathology in vivo,” American Journal of Reproductive Immunology, vol. 65, no. 2, pp. 118–126, 2011.
- J. U. Igietseme and A. Murdin, “Induction of protective immunity against Chlamydia trachomatis genital infection by a vaccine based on major outer membrane protein-lipophilic immune response-stimulating complexes,” Infection and Immunity, vol. 68, no. 12, pp. 6798–6806, 2000.
- D. Longbottom, “Chlamydial vaccine development,” Journal of Medical Microbiology, vol. 52, no. 7, pp. 537–540, 2003.
- C. Escalante-Ochoa, R. Ducatelle, and F. Haesebrouck, “The intracellular life of Chlamydia psittaci: how do the bacteria interact with the host cell?” FEMS Microbiology Reviews, vol. 22, no. 2, pp. 65–78, 1998.
- A. F. Swanson and C. C. Kuo, “Evidence that the major outer membrane protein of Chlamydia trachomatis is glycosylated,” Infection and Immunity, vol. 59, no. 6, pp. 2120–2125, 1991.
- L. J. Berry, D. K. Hickey, K. A. Skelding et al., “Transcutaneous immunization with combined cholera toxin and CpG adjuvant protects against Chlamydia muridarum genital tract infection,” Infection and Immunity, vol. 72, no. 2, pp. 1019–1028, 2004.
- S. Pal, C. J. Luke, A. G. Barbour, E. M. Peterson, and L. M. De La Maza, “Immunization with the Chlamydia trachomatis major outer membrane protein, using the outer surface protein A of Borrelia burgdorferi as an adjuvant, can induce protection against a chlamydial genital challenge,” Vaccine, vol. 21, no. 13-14, pp. 1455–1465, 2003.
- G. Sun, S. Pal, J. Weiland, E. M. Peterson, and L. M. de la Maza, “Protection against an intranasal challenge by vaccines formulated with native and recombinant preparations of the Chlamydia trachomatis major outer membrane protein,” Vaccine, vol. 27, no. 36, pp. 5020–5025, 2009.
- D. K. Hickey, F. E. Aldwell, and K. W. Beagley, “Transcutaneous immunization with a novel lipid-based adjuvant protects against Chlamydia genital and respiratory infections,” Vaccine, vol. 27, no. 44, pp. 6217–6225, 2009.
- P. Ralli-Jain, D. Tifrea, C. Cheng, S. Pal, and L. M. de la Maza, “Enhancement of the protective efficacy of a Chlamydia trachomatis recombinant vaccine by combining systemic and mucosal routes for immunization,” Vaccine, vol. 28, no. 48, pp. 7659–7666, 2010.
- M. Tuffrey, F. Alexander, W. Conlan, C. Woods, and M. Ward, “Heterotypic protection of mice against chlamydial salpingitis and colonization of the lower genital tract with a human serovar F isolate of Chlamydia trachomatis by prior immunization with recombinant serovar L1 major outer-membrane protein,” Journal of General Microbiology, vol. 138, no. 8, pp. 1707–1715, 1992.
- A. K. Murthy, J. P. Chambers, P. A. Meier, G. Zhong, and B. P. Arulanandam, “Intranasal vaccination with a secreted chlamydial protein enhances resolution of genital Chlamydia muridarum infection, protects against oviduct pathology, and is highly dependent upon endogenous gamma interferon production,” Infection and Immunity, vol. 75, no. 2, pp. 666–676, 2007.
- F. Follmann, A. W. Olsen, K. T. Jensen, P. R. Hansen, P. Andersen, and M. Theisen, “Antigenic profiling of a Chlamydia trachomatis gene-expression library,” Journal of Infectious Diseases, vol. 197, no. 6, pp. 897–905, 2008.
- A. W. Olsen, F. Follmann, K. Jensen et al., “Identification of CT521 as a frequent target of Th1 cells in patients with urogenital Chlamydia trachomatis infection,” Journal of Infectious Diseases, vol. 194, no. 9, pp. 1258–1266, 2006.
- D. K. Hickey, F. E. Aldwell, and K. W. Beagley, “Oral immunization with a novel lipid-based adjuvant protects against genital Chlamydia infection,” Vaccine, vol. 28, no. 7, pp. 1668–1672, 2010.
- S. C. Knight, S. Iqball, C. Woods, A. Stagg, M. E. Ward, and M. Tuffrey, “A peptide of Chlamydia trachomatis shown to be a primary T-cell epitope in vitro induces cell-mediated immunity in vivo,” Immunology, vol. 85, no. 1, pp. 8–15, 1995.
- H. Su, M. Parnell, and H. D. Caldwell, “Protective efficacy of a parenterally administered MOMP-derived synthetic oligopeptide vaccine in a murine model of Chlamydia trachomatis genital tract infection: serum neutralizing IgG antibodies do not protect against chlamydial genital tract infection,” Vaccine, vol. 13, no. 11, pp. 1023–1032, 1995.
- A. M. Watts and R. C. Kennedy, “DNA vaccination strategies against infectious diseases,” International Journal for Parasitology, vol. 29, no. 8, pp. 1149–1163, 1999.
- J. B. Ulmer, T. M. Fu, R. R. Deck et al., “Protective CD4(+) and CD8(+) T cells against influenza virus induced by vaccination with nucleoprotein DNA,” Journal of Virology, vol. 72, no. 7, pp. 5648–5653, 1998.
- V. Dufour, “DNA vaccines: new applications for veterinary medicine,” Veterinary Sciences Tomorrow, vol. 1, pp. 1–19, 2001.
- H. C. J. Ertl and Z. Q. Xiang, “Genetic immunization,” Viral Immunology, vol. 9, no. 1, pp. 1–9, 1996.
- T. Martin, S. E. Parker, R. Hedstrom et al., “Plasmid DNA malaria vaccine: the potential for genomic integration after intramuscular injection,” Human Gene Therapy, vol. 10, no. 5, pp. 759–768, 1999.
- L. A. Babiuk, R. Pontarollo, S. Babiuk, B. Loehr, and S. Van Drunen Littel-van den Hurk, “Induction of immune responses by DNA vaccines in large animals,” Vaccine, vol. 21, no. 7-8, pp. 649–658, 2003.
- S. Pal, K. M. Barnhart, Q. Wei, A. M. Abai, E. M. Peterson, and L. M. De La Maza, “Vaccination of mice with DNA plasmids coding for the Chlamydia trachomatis major outer membrane protein elicits an immune response but fails to protect against a genital challenge,” Vaccine, vol. 17, no. 5, pp. 459–465, 1999.
- D. J. Zhang, X. Yang, C. Shen, H. Lu, A. Murdin, and R. C. Brunham, “Priming with Chlamydia trachomatis major outer membrane protein (MOMP) DNA followed by MOMP ISCOM boosting enhances protection and is associated with increased immunoglobulin A and Th1 cellular immune responses,” Infection and Immunity, vol. 68, no. 6, pp. 3074–3078, 2000.
- K. Schautteet, Epidemiological Research on Chlamydiaceae in Pigs and Evaluation of a Chlamydia trachomatis DNA vaccine, Ghent University, Ghent, Belgium, 2010.
- K. Schautteet, E. Stuyven, D. S. A. Beeckman et al., “Protection of pigs against Chlamydia trachomatis challenge by administration of a MOMP-based DNA vaccine in the vaginal mucosa,” Vaccine, vol. 29, no. 7, pp. 1399–1407, 2011.
- D. Vanrompay, T. Q. T. Hoang, L. De Vos et al., “Specific-pathogen-free pigs as an animal model for studying Chlamydia trachomatis genital infection,” Infection and Immunity, vol. 73, no. 12, pp. 8317–8321, 2005.
- M. Donati, V. Sambri, M. Comanducci et al., “DNA immunization with pgp3 gene of Chlamydia trachomatis inhibits the spread of chlamydial infection from the lower to the upper genital tract in C3H/HeN mice,” Vaccine, vol. 21, no. 11-12, pp. 1089–1093, 2003.
- M. Comanducci, R. Cevenini, A. Moroni et al., “Expression of a plasmid gene of Chlamydia trachomatis encoding a novel 28 kDa antigen,” Journal of General Microbiology, vol. 139, no. 5, pp. 1083–1092, 1993.
- G. O. Ifere, Q. He, J. U. Igietseme et al., “Immunogenicity and protection against genital Chlamydia infection and its complications by a multisubunit candidate vaccine,” Journal of Microbiology, Immunology and Infection, vol. 40, no. 3, pp. 188–200, 2007.
- Z. Li, S. Wang, Y. Wu, G. Zhong, and D. Chen, “Immunization with chlamydial plasmid protein pORF5 DNA vaccine induces protective immunity against genital chlamydial infection in mice,” Science in China C, vol. 51, no. 11, pp. 973–980, 2008.
- R. T. Gray, K. W. Beagley, P. Timms, and D. P. Wilson, “Modeling the impact of potential vaccines on epidemics of sexually transmitted Chlamydia trachomatis infection,” Journal of Infectious Diseases, vol. 199, no. 11, pp. 1680–1688, 2009.