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Journal of Biomedicine and Biotechnology
Volume 2010 (2010), Article ID 591348, 8 pages
http://dx.doi.org/10.1155/2010/591348
Research Article

Development of Th1 Imprints to rBCG Expressing a Foreign Protein: Implications for Vaccination against HIV-1 and Diverse Influenza Strains

1Prince of Wales Clinical School, University of New South Wales, NSW2052 Sydney, Australia
2Department of Microbiology and Immunology, University of Saskatchewan, Saskatoon, SK, S7N5E5, Canada
3Department of Pathology and Laboratory Medicine, University of Saskatchewan, Saskatoon, SK, S7N0W8, Canada

Received 5 December 2009; Revised 14 March 2010; Accepted 22 March 2010

Academic Editor: Hanchun Yang

Copyright © 2010 Carl Power 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.

Abstract

We demonstrate here that immunizing naïve mice with low numbers of recombinant Bacille Calmette-Guérin (rBCG) expressing -galactosidase ( -gal) generates predominant Th1 responses to both BCG and -gal whereas infection with high numbers generates a mixed Th1/Th2 response to both BCG and -gal. Furthermore, the Th1 response to both BCG and -gal is stable when mice, pre-exposed to low numbers of rBCG, are challenged four months later with high numbers of rBCG. Thus the Th1/Th2 phenotypes of the immune responses to -gal and to BCG are “coherently” regulated. Such rBCG vectors, encoding antigens of pathogens preferentially susceptible to cell-mediated attack, may be useful in vaccinating against such pathogens. We discuss vaccination strategies employing rBCG vectors that are designed to provide protection against diverse influenza strains or numerous variants of HIV-1 and consider what further experiments are essential to explore the possibility of realizing such strategies.

1. Introduction

A rational approach to vaccination against a pathogen is contingent upon a knowledge of the immunological correlates that discriminate between immunity able to contain the pathogen and immunity that fails to do so. Effective vaccination must guarantee the former type of immunity under circumstance where the latter type of immunity would be generated upon natural infection of the naïve individual [1]. Effective vaccination of people, against a diversity of pathogens, is achieved through guaranteeing a rapid and large antibody, Th2 response upon natural infection by the pathogen. Such vaccination is effective only when antibody is able to contain the pathogen and/or neutralize the toxins the pathogen produces. However, there are other situations, following infection by some intracellular pathogens or the development of cancer, where the correlates of protection are a predominant cell-mediated, CTL, Th1 response and where responses with a substantial Th2, antibody component, are associated with chronic or progressive disease [2]. In these cases, it would appear that effective vaccination must generate a Th1 imprint upon the immune system that is stable upon natural infection by the pathogen [3].

Mycobacterium bovis is responsible for tuberculosis of cattle. An attenuated form of M. bovis, named BCG, is currently the only available vaccine against Mycobacterium tuberculosis, the pathogen primarily responsible for human tuberculosis. Billions of individuals worldwide have been inoculated with BCG in attempts to provide protection against tuberculosis and leprosy. Moreover, these bacteria can be used as vectors that express antigens of diverse pathogens to raise immunity against these antigens. Several recombinant BCG vectors have been constructed for vaccination against a variety of bacterial, viral, or parasitic pathogens [4].

There are several advantages in using rBCG vectors. Not only does BCG act as an adjuvant, but its slow replication allows for persistent, low level delivery of antigen to the host over a considerable time. Many observations show, in diverse systems, that chronic stimulation with low amounts of antigen can lead to the establishment of Th1 imprints [2, 3, 57]. Additionally, advances in expression and delivery of antigen by rBCG, hence increasing the availability of the encoded antigens to the host immune system, have allowed the development of vaccine vectors superior to those of the past [4]. We are also encouraged to explore the use of rBCG vectors in developing strategies of vaccination by the remarkable safety record of BCG as a vaccination agent [8].

A critical question, when considering the use of rBCG vectors to immunize against the encoded protein, is the relationship between the nature of the immune response to BCG and the nature of the response to the encoded protein. This is particularly critical in those cases where there are grounds for believing that the Th1/Th2 phenotype of the response to the encoded antigen is likely critical to the degree of protection provided by vaccination. It has been proposed that the Th1/Th2 phenotype of the responses to BCG and the encoded protein may be coordinately determined [1], a phenomenon referred to as coherence. We set out to explore whether, employing rBCG encoding -galactosidase as a model rBCG vector, the Th1/Th2 phenotypes of the immune responses to BCG and to -galactosidase are coherently regulated. Should this be the case, it would lay the foundation for further studies aimed at examining whether rBCG vectors could be employed to establish Th1 imprints against those pathogens preferentially susceptible to predominant cell-mediated, Th1 responses.

2. Materials and Methods

2.1. Mice

Female mice were used in all experiments. BALB/cJ mice were obtained from the animal colony at the Department of Microbiology and Immunology, University of Saskatchewan. All mice were housed at the animal care facility within the Department and were at least 6 weeks old at the time of immunization. Animal care and treatment were in accordance with standards approved by the Canadian Council on Animal Care.

2.2. Growth and Enumeration of rBCG

Dr. Emil Skamene of McGill University provided M. bovis strain BCG Montreal. The mycobacteria were propagated in Dubos medium containing 0.5% bovine serum albumin and 0.05% Tween 80. Bacteria were enumerated by plating various dilutions on Dubos agar plates after sonication for five seconds at a power output of 5 and 50% duty cycle to break up clusters of bacteria. Colonies were counted fourteen days after plating, and consequently numbers of bacteria are expressed as cfu.

2.3. Immunizations

Fourteen-day cultures of BCG or rBCG were used for injections. The cells were pelleted by centrifugation at 8000 g for 30 minutes and washed three times by repeated resuspension in saline containing 0.05% Tween 80 followed by centrifugation at 8000 g for 20 minutes. After the final wash, the mycobacteria were resuspended in 1/100 of the original volume of culture, and serial dilutions were performed from this stock as needed. BCG immunizations were performed by either intradermal (i.d.) or intravenous (i.v.) route. For i.d. injection, hair was removed from the abdomen using a commercial depilatory two days prior to injection. Injections were done using a 1 cc syringe with a 30-gauge needle attached. Mice were anesthetized, and the skin of the abdomen was gently stretched to prevent it from bunching up in front of the needle. With the bevel of the needle facing upward, the needle was inserted several millimeters horizontally into the skin and 25–50  l of the BCG suspension containing the appropriate number of cfu was injected. For i.v. injection, the desired number of BCG cfu were injected in a 50  l volume into the lateral tail vein using a 28-gauge needle.

Mice were immunized by the i.p. route with recombinant -gal (Sigma Chemicals, St. Louis, MO), either as a soluble protein in phosphate-buffered saline (PBS) or adsorbed to the aluminum hydroxide gel adjuvant, Alhydrogel (Superfos Biosector, Vedbaek, Denmark) as indicated in the legend to Figure 6.

2.4. ELISPOT Assay for Detection and Enumeration of Antigen-Dependent IFN - and IL-4-Secreting Cells

The ELISPOT assay for enumeration of BCG-specific cytokine producing lymphocytes was performed on spleen cells as previously described in detail [9]. For detection of -gal-specific cytokine-producing cells, the procedure was identical except that purified soluble -gal (Sigma Chemicals) was used at 1  g/well for stimulation of lymphocytes.

2.5. Analysis of Antimycobacterial or Anti- -gal Antibodies by Enzyme Immunoassay

Blood from normal or infected mice was collected by tail bleeding into serum separator tubes (Becton Dickinson, Rutherford, NJ). After allowing the samples to clot for at least several hours, individual serum samples were harvested by centrifugation at approximately 5000 g for 60 seconds. Sera were stored at C until use. The IgG1 and IgG2a serum antibody titers were determined using an ELISA. Immulon-4 96-well polystyrene plates (Dynatech Laboratories, Chantilly, VA) were coated with either BCG antigen or with soluble -gal antigen at a concentration of 1  g/well in 100  l of PBS and the procedure was performed as described in [10]. The titer was determined by plotting optical density against the log of the dilution factor for each sample. The endpoint titer was assigned as the point on the line at which the optical density was 0.5 above the value for wells to which no serum was added.

2.6. Mycobacterial Expression Vectors

Dr. Mark Hanson of MedImmune, Gaithersberg, MA, kindly provided the mycobacterial expression vector pMV361::LacZ [11]. Vector pMV361 is a chromosomal integrating vector in which inserted genes are expressed as a fusion protein with the first six amino acids of the mycobacterial heat shock protein 60 (Hsp60).

2.7. Transformation of Competent M. bovis BCG

The method of Parish and Stoker [12] was used to prepare electroporation-competent BCG. Transformation of competent BCG was performed by electroporation using the Gene Pulser II (BioRad). Electroporation-competent BCG was removed from the freezer and immediately placed on ice for several minutes to allow samples to thaw. One microgram of plasmid DNA was added to the tube, and the contents were mixed and placed on ice for ten minutes. The mixture was transferred to a chilled, 2 mm gap electroporation cuvette (VWR scientific, Toronto, ON). The bacteria were subjected to a pulse of 3.5 kV, 25  F, at a resistance of 1000  [12]. The cuvette was incubated on ice for ten minutes before the contents were transferred to a separate tube and diluted with 3 ml of Middlebrook 7H9 media (Difco, Detroit, MI) with 0.5% Tween 80 and OADC supplement (Difco). The mixture was incubated at C for 3 h to allow for antibiotic expression. Cells were harvested by centrifugation at 3000 g for ten minutes and plated on Middlebrook 7H10 agar plates with OADC and 10  g/ml of kanamycin [12]. The plates were sealed with parafilm and incubated at C for 21–28 days to allow colonies to grow.

3. Results

Figures 1 and 2 show the number of BCG- and -gal-specific IFN - and IL-4-producing cells in the spleens of mice nine weeks after immunization with different doses of rBCG (either rBCG gal or rBCGHgag). Immunization with both low and high doses of rBCG gal induced not only BCG-specific but also -gal-specific cytokine-producing cells, indicating that the -gal is expressed in vivo at a level sufficient to induce an immune response. The immune response to different doses of rBCG given by i.v. (Figure 1) and i.d. (Figure 2) immunization is qualitatively different. Regardless of the route, high doses of rBCG gal induce a mixed IFN and IL-4 response while lower doses induce a predominantly IFN response to both BCG and the expressed -gal antigen. Although the numbers of -gal-specific spot forming cells are low in rBCG gal immunized mice, they represent a significant portion of the response to the rBCG gal, particularly in mice immunized by the i.d. route. Mice immunized with BCG transformed with a control vector BCGHgag, not expressing -gal (Figure 1(d)), show no response to -gal while cells from unimmunized control mice (shown in Figure 2(d)) do not respond to either the BCG-lysate antigen or to the -gal antigen. Only mice immunized with the high doses of rBCG gal had significant antibody titers to -gal (data not shown), indicating that the antibody response is indeed attributable to immunization with rBCG gal, and that only higher doses induce antibody production. Similarly, high doses of rBCG were required for induction of BCG-specific antibody production, demonstrating that the humoral response to -gal follows that induced for the BCG.

fig1
Figure 1: Immune response of four individual mice per group after i.v. immunization with different doses of recombinant BCG (rBCG gal) or control rBCG expressing HIV gag protein (rBCGHgag). Immunization dose is indicated below each graph. Mice were immunized as indicated under each graph. After 9 weeks, the mice were killed and the number of -gal- and BCG-specific IFN - and IL-4-producing cells in their spleens was determined by ELISPOT assay. The response in mice given a high dose of BCG transformed with a control vector containing the HIV gag sequence is also shown. Open bars—IFN response to BCG; Black bars—IFN response to -gal; Dark gray bars—IL-4 response to BCG; Light gray bars—IL-4 response to -gal. All values were corrected for background by subtracting the number of spots observed in wells without antigen. Results are representative of two independent experiments.
fig2
Figure 2: Immune response of four individual mice per group after i.d. immunization with different doses of recombinant BCG gal. Mice were immunized as indicated under each graph, with an unimmunized control shown. After 9 weeks, the mice were killed and the number of -gal- and BCG-specific IFN - and IL-4-producing cells in their spleens was determined by ELISPOT assay. Open bars—IFN response to BCG; Black bars—IFN response to -gal; Dark gray bars—IL-4 response to BCG; Light gray bars—IL-4 response to β-gal. All values were corrected for background by subtracting the number of spots observed in wells without antigen. Results are representative of two independent experiments.

We wished to determine if low-dose immunization with rBCG gal could establish immune deviation such that the IFN -dominant response initially induced by the low-dose vaccination would be maintained upon subsequent challenge with a dose of rBCG gal that induces a mixed IFN /IL-4 response in naïve mice. Mice immunized with different doses of rBCG by the i.d. route were challenged four months later with a high dose of rBCG gal, also given intradermally. The immune response was assayed at 16 weeks postchallenge. Mice that were immunized with low doses by the i.d. route (Figure 3) maintained a dominant IFN response to BCG antigen and to -gal after the challenge, which was distinct from the mixed IFN /IL-4 response of control mice that received only the challenge dose, demonstrating immune deviation toward a cell-mediated response. The ratio of IFN - to IL-4-producing cells (means within each group) are depicted in Figure 4. Even after challenge with the high dose of rBCG gal, the mice that were immunized previously with a low dose of rBCG have a tenfold higher IFN response compared to control mice or those mice given only the high challenge dose. These results demonstrate that, once established, the dominant IFN response induced by low-dose vaccination is not easily deviated to an IL-4 response upon challenge. The anti- -gal serum antibody titers from the mice of Figure 3 are shown in Figure 5. Note the prominence of IgG2a antibody in the serum of mice immunized with a low dose of rBCG before challenge, compared to the control mice given only the high dose. This is consistent with the prominence of IFN -producing cells in mice pretreated with low doses of rBCG, as class switching to IgG2a is associated with IFN production in mice [3].

fig3
Figure 3: Immune response of individual mice vaccinated with different doses of rBCGβgal after subsequent i.d. challenge with a high dose of rBCGβgal. Each group of mice was initially given an i.d. vaccination dose of rBCGβgal as indicated below each graph with a control group receiving challenge dose only shown. After 4 months, the mice were challenged with approximately 2 107 rBCGβgal cfu given i.d. After an additional 16 weeks, the mice were killed and the number of β-gal- and BCG-specific IFNγ- and IL-4-producing cells in their spleens was determined by ELISPOT assay. Open bars—IFNγ response to BCG; Black bars—IFNγ response to β-gal; Dark gray bars—IL-4 response to BCG; Light gray—IL-4 response to β-gal. All values were corrected for background by subtracting the number of spots observed in wells without antigen. Results are representative of two independent experiments.
591348.fig.004
Figure 4: Ratio of IFN to IL-4 spots in the mice depicted in Figure 3. Ratios were calculated as the mean number of antigen-specific IFN spots/the mean number of IL-4 spots within each group of mice. Open circles and filled circles represent BCG- and gal-specific IFN  : IL-4 ratios, respectively.
fig5
Figure 5: Serum antibody responses of mice to β-gal after immunization with different doses of rBCG by the i.d. route, and subsequent challenge with a high dose of rBCG by the same route. Mice were immunized initially with doses indicated below each graph with age-matched control mice receiving only challenge dose shown. After 16 weeks, all groups were challenged with 2 107 rBCG given i.d. Serum was collected at the time the mice were killed, 16 weeks after the challenge. Open bars show IgG1 titers while black bars depict IgG2a titers.
fig6
Figure 6: Number of IFNγ- and IL-4-producing cells in mice immunized i.p. with soluble β-gal (A) and β-gal adsorbed to alum as an adjuvant (B). Soluble β-gal was administered twice five days apart, while β-gal/alum was administered only once. Dose of β-gal administered in each experiment is indicated (10  g or 100  g). Mice were killed 11 days after the initial injection, and antigen-specific cytokine-producing spleen cells were enumerated by ELISPOT assay. Open bars represent IFNγ spots and black bars represent IL-4 spots. Results are representative of three separate experiments.

We compared the immune response to -gal in mice immunized with rBCG gal and in mice immunized with purified -gal using other methods that might be acceptable for immunization of humans. Figure 6 shows the immune response in mice immunized with purified -gal given in alum as an adjuvant. In both cases, immunization was by the i.p. route. Soluble -gal did not induce a significant immune response in any of the mice immunized with this preparation (data not shown). -gal in alum, however, induced predominantly IL-4-producing cells in mice, at even the low dose used. This is not unexpected as alum is particularly effective at inducing Th2 responses [13]. However, these results exemplify potential problems in achieving a desirable Th1 response in humans with current vaccination procedures.

4. Discussion

Previous studies have shown that the Th1/Th2 phenotype of the immune response to BCG, generated in very young and in adult mice, depends upon the dose of BCG administered, as assessed following infection by several different routes [10]. Infection with relatively low numbers of BCG generates a predominant Th1 response and with higher numbers a mixed Th1/Th2 response. Here we show that the Th1/Th2 phenotypes of the immune responses to BCG and to -gal similarly depend upon the number of rBCG employed for infection and that the Th1/Th2 phenotypes of the responses to BCG and to -gal appear to be coherent. Our studies show that rBCG can be used to preferentially generate a Th1 response to the encoded antigen by infecting with relatively low doses of rBCG. We now consider the potential use of this strategy in vaccination against HIV-1 and influenza viruses.

In looking at current views, it appears that there are two main, contradictory, positions as to how effective vaccination against HIV-1 might be achieved. Most suggest the combination of cell-mediated immunity, in the form of CTL and neutralizing antibody, will provide optimal protection. Thus, vaccination should ensure such a response is mounted upon natural exposure to the virus. It is well known that neutralizing antibody can be generated, but that HIV-1 has a means of generating viral variants very quickly. As such, neutralizing antibody generated against the original variant encountered will be effective against this particular variant, but usually is ineffective against newly arising variants that become dominant through the course of the infection.

The contrasting view we favor is that vaccination, in order to be effective, must guarantee a predominant Th1 response, associated with potent CTL generation, upon HIV-1 infection. We think three lines of reasoning support this view. Firstly, there are highly exposed and infected individuals who produce predominant and stable Th1, CTL responses, but who are symptom-free. A prime illustration of such a group is a cohort of female sex workers in Nairobi, whose immune state has been extensively characterized [14, 15]. What is additionally remarkable about this group of individuals is that they do not seroconvert and remain healthy over many years despite numerous exposures to major viral variants or clades of HIV-1 due to the nature of their work. Secondly, all individuals infected with HIV-1 are healthy during the period when their immune system mounts a predominant Th1, CTL response, before they seroconvert and enter the progressive stages of disease [16]. Both observations strongly support the idea that a predominant Th1, CTL response can contain HIV-1. Why then not aim for having the best of both worlds, both CTL and neutralizing antibody, as most suggest? It is an assumption, and one that we feel is highly questionable, that this is possible. Distinct CD T cell subsets tend to inhibit each others’ generation and often each others’ effector activities [1]. It may not be possible to have the best of both worlds, involving a mixed Th1/Th2 response, with optimal production of CTL immunity and neutralizing antibody. We think it best to conclude, in accordance with natural situations in which the virus is contained, and infected individuals remain symptom-free, that a predominant Th1, CTL response is optimally protective. We employ this proposition as a starting point for considering how effective vaccination might be achieved.

In the case of influenza virus, that causes an acute infection, it seems antibody can be highly protective. Antibody is usually not produced in sufficient amounts upon infection of naïve individuals to prevent pathological symptoms, which is why immunization against the virus causing the current epidemic is effective in preventing illness. Individuals who have been infected during the last epidemic, but not immunized against the virus causing the current epidemic, are highly primed to produce antibody. The antibody produced is highly effective in neutralizing the influenza strain causing the previous epidemic, but not the virus causing the current epidemic. This makes eminent sense from an epidemiological point of view. It is just because the current influenza strain can stimulate the production of this antibody, ineffective in its own neutralization, that the virus can multiply unimpeded in the individual, primed by a previous infection, with the consequential spread of the virus through the population. An appreciation of these facts underlies the formulation of current policy. The aim is to achieve immunization against the strain causing the current epidemic as soon as it has been identified. This policy is sound, but its realization is extremely expensive and poses considerable logistical problems, clearly illustrated throughout the most recent influenza H1N1 pandemic.

The CTL response against influenza involves, in large measure, a response against peptides derived from viral proteins that do not vary greatly between strains, such as peptides derived from the nuclear protein, NP [17]. The possibility might therefore be considered that vaccination resulting in a sustained and effective CTL response upon infection by diverse variants might be effective against all variants. An intriguing report supports this possibility. DNA immunization of mice against NP results in a predominant Th1, CTL response on challenge with different viral variants and resistance [18]. Thus generating stable Th1 imprints against influenza might result in protection against diverse viral variants.

The observations reported here and our considerations on how vaccines against diverse clades of HIV-1 and strains of influenza might be achieved by causing Th1 imprints lead us to suggest that attempts at realizing a low-dose rBCG vaccination strategy is worthy of further exploration. We showed in this paper that infection with low numbers of rBCG generated not only predominant Th1 responses but also Th1 imprints as assessed by the predominant Th1 responses observed upon a subsequent challenge with a high number of rBCG that generate mixed Th1/Th2 responses in naïve animals. We consider the next important step in assessing the plausibility of this strategy will be to examine whether rBCG can provide protection against a pathogenic infection. There are mouse models of influenza infection. We hope to examine, employing established systems, whether infection of mice with low numbers of rBCG vectors, encoding conserved proteins of influenza virus, can generate Th1 imprints, as assessed by infection with a normally pathogenic challenge of influenza virus, and whether such imprints provide protection against diverse viral variants.

Acknowledgments

The authors thank Dr. Mark Hansen for providing the mycobacterial plasmids and D. Yurkowski for valuable technical assistance. This work was supported by a CIHR grant held by Peter Bretscher.

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