Cytotoxic T Lymphocytes and Vaccine DevelopmentView this Special Issue
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Hong Qin, Pramod N. Nehete, Hong He, Bharti Nehete, Stephanie Buchl, Soung-chul Cha, Jagannadha K. Sastry, Larry W. Kwak, "Prime-Boost Vaccination Using Chemokine-Fused gp120 DNA and HIV Envelope Peptides Activates Both Immediate and Long-Term Memory Cellular Responses in Rhesus Macaques", BioMed Research International, vol. 2010, Article ID 860160, 7 pages, 2010. https://doi.org/10.1155/2010/860160
Prime-Boost Vaccination Using Chemokine-Fused gp120 DNA and HIV Envelope Peptides Activates Both Immediate and Long-Term Memory Cellular Responses in Rhesus Macaques
HIV vaccine candidates with improved immunogenicity and induction of mucosal T-cell immunity are needed. A prime-boost strategy using a novel HIV glycoprotein 120 DNA vaccine was employed to immunize rhesus macaques. The DNA vaccine encoded a chimeric gp120 protein in fusion with monocyte chemoattractant protein-3, which was hypothesized to improve the ability of antigen-presenting cells to capture viral antigen through chemokine receptor-mediated endocytosis. DNA vaccination induced virus-reactive T cells in peripheral blood, detectable by T cell proliferation, INF ELISPOT and sustained IL-6 production, without humoral responses. With a peptide-cocktail vaccine containing a set of conserved polypeptides of HIV-1 envelope protein, given by nasogastric administration, primed T-cell immunity was significantly boosted. Surprisingly, long-term and peptide-specific mucosal memory T-cell immunity was detected in both vaccinated macaques after one year. Therefore, data from this investigation offer proof-of-principle for potential effectiveness of the prime-boost strategy with a chemokine-fused gp120 DNA and warrant further testing in the nonhuman primate models for developing as a potential HIV vaccine candidate in humans.
Acquired immunodeficiency syndrome (AIDS) is a life-threatening viral disease caused by a severely impaired immune defense mechanism resulting from devastation of CD4+ T lymphocytes by human immunodeficiency virus-1 (HIV-1). A fundamental concept in controlling AIDS development is to prevent the loss of CD4+ T cells, which may be achieved by inhibiting intracellular viral replication and eliminating virus-infected cells. A therapeutic HIV vaccine that aims at activating adaptive T-cell immunity to prevent intercellular spread of viruses is therefore required to curb the rapid worldwide spread of this disease. Although enormous efforts have been made to test a variety of vaccine strategies, the generation of an HIV vaccine with potent antiviral effects remains elusive. One major obstacle hampering vaccine development is the low magnitude of vaccine-elicited immunity. To overcome this issue, current attention is mainly focused on developing strategies to enhance the immunogenicity of HIV vaccine formulations and the induction of mucosal immunity. These attempts have included the delivery of HIV antigen genes by live recombinant adenovirus or mycobacterium, resulting in an improved HIV-specific immune response [1, 2]. The critical role of dendritic cells in initiating the adaptive immune response is well recognized by their function in capturing, processing, and presenting antigens. Other strategies that specifically target delivery of antigens to dendritic cells may therefore increase the potency of antigen-specific immune responses [3–5]. Chemokines are a family of chemotactic polypeptides that facilitate the homing of antigen-bearing dendritic cells to draining lymph nodes. Chemokine-induced signal transduction is triggered by the binding of chemokines with G-protein—coupled receptors and is subsequently terminated by the clathrin-mediated endocytosis of the chemokine-receptor complex. Given these features of chemokine receptors on dendritic cells, we previously described achievement of triggering potent T-cell responses by fusion of candidate, otherwise non-immunogenic antigens with chemokines, hypothesizing that the chemokine motif in the chimeric proteins would direct antigens to dendritic cells or other antigen-presenting cells in the body. Specifically, using HIV-1 89.6 envelope glycoprotein 120 as a model antigen, we verified that genetic fusion of this candidate HIV antigen with chemokines dramatically increased its immunogenicity in mice . Both systemic and mucosal HIV-specific T-cell immunities were elicited upon immunizing mice with plasmid DNA encoding the full-length gp120 gene fused with monocyte chemotactic protein-3 (MCP3). In the present proof-of-principle pilot study, we show for the first time that an MCP3-fused gp120 DNA vaccine elicited virus-specific T-cell immunity in rhesus macaques at a dose of only 20 g of plasmid DNA. The elicited T-cell response was boosted by nasal administration of a peptide-cocktail consisting of six highly conserved epitopes of the HIV-1 envelope protein. A highly desirable feature of this prime-boost strategy was the induction of long-term mucosal T-cell immunity.
2. Materials and Methods
2.1. Vaccination of Animals
The macaque study was performed under a protocol approved by the Institutional Animal Care and Use Committee of The University of Texas, M. D. Anderson Cancer Center. Two male rhesus macaques of Indian origin (designated J8 and J160) from the institution’s specific pathogen-free breeding colony at the Science Park campus in Bastrop, Texas were used for the study. The animal facility is fully accredited by the Association for Assessment and Accreditation of Laboratory Animal Care International. The plasmid DNA encoding MCP3-fused gp120 was generated as described in our previous studies . The DNA was precipitated in the presence of 1 m gold particles (BioRad, Hercules, CA) and the polycation spermide by the addition of calcium chloride. The DNA-attached gold particles were washed and resuspend in ethanol, coated onto the inner wall of Gold-Coat tubing (BioRad), dried and cut into 0.5” length cartridge. These cartridges were inserted into the cartridge holder of the Helio Gene Gun (BioRad). By helium discharge the DNA was directly delivered into skin. The particle-coated plasmid DNA was delivered intradermally using helium gene gun (BioRad) at 400 psi. A total amount of approximate 20 g DNA was evenly distributed at shaved areas on each arm or leg. The booster dose of the peptide-cocktail vaccine consists of six highly conserved HIV-1 envelope peptides (each at 100 g/dose/macaque). The peptide synthesis, amino acid sequence, and immunogenicity were reported previously [7–9]. The peptide-cocktail was administered by nasogastric route along with a mutant cholera toxin, CT2* (10 g/dose/monkey) that we reported previously to be a safe and effective mucosal adjuvant in murine and primate models [10, 11] in 600 L sterile PBS.
2.2. Collection of Samples
Peripheral venous blood samples collected in sodium heparin at different time points were centrifuged to separate plasma and buffy coat. Peripheral blood mononuclear cells (PBMC) were separated from buffy coat by centrifugation through Ficoll-Paque density gradients and were used for various immune assays. Also, serum samples were collected and stored at −C for analysis of the neutralizing antibody. The intraepithelial lymphocytes (IEL) from the colon biopsy sections of the macaques were isolated by using modifications of previously described procedures . Briefly, 10–15 samples of colon biopsy (2 mm each) were collected and rinsed in cold PBS. The tissue was treated with dithiothreitol (DTT, 1.5 mg/mL) in Hank’s balanced salt solution (HBSS) for 30 minute at RT with agitation to remove mucus. The tissue were then treated with 0.75 mM EDTA in Ca2+- and Mg2+-free HBSS at RT for 60 minute with stirring. After the treatment, the supernatants containing epithelial cells were removed and digested with 15 U of collagenase D and DNAse I in complete RPMI 1640 medium containing 100 U of penicillin and 100 U of streptomycin per ml, 5 ml L-glutamine, 5 ml HEPES buffer, and 10% FCS at C with rapid shaking for 2 hours. The resulting cell suspensions were passed through stainless steel screen cups to remove the residual tissue fragments. The cells were washed and resuspended in complete RPMI 1640 medium and enriched for lymphocytes by isotonic discontinuous Percoll (Sigma) density gradients (35 and 60% [vol/vol]) at 1,000 g for 20 minute at C. The lymphocyte band at the interface between the 35 and 60% Percoll layers was collected. Viability of lymphocytes was greater than 95% as determined by the Trypan blue dye exclusion method. Aliquots of freshly-isolated cells were stained with fluorescently-labeled antibodies for flow cytometry analysis.
2.3. Proliferation Assay
Proliferative responses of PBMC isolated from immunized macaques were determined using the standard [3H] thymidine incorporation assay as described earlier . Briefly, 100 L aliquots of the cell suspensions (1 × 105 cells in complete RPMI) were dispersed into triplicate wells of a round-bottom 96-well microtiter plate and incubated with the HIV-1 envelope peptides (10 g/mL final concentration) as a single mixture (designated as pep-mix) and the cell-free heat-inactivated SHI (equivalent to 50 ng/ml final concentration of p27) prepared by incubating for 60 minute at C. The proliferative response was calculated as the fold increase in radioactivity with the test antigen over that for cells cultured in the medium alone and is represented as the stimulation index (SI). The responses to peptides were considered positive when the SI values are 2.0 or greater, and also 2.0 above the value for the negative control peptide (from human papilloma virus at 10 mg/mL final concentration) or medium control used in the same experiment. No differences were observed between the negative control peptide and culture medium as control treatments.
2.4. Measurement of IFN-γ Production by ELISPOT Assay
PBMC isolated from immunized macaques were stimulated with the mixture of the HIV-1 envelope peptides and cell-free, heat-inactivated SHI for determining the antigen-specific interferon- (IFN-γ)–producing cells by the ELISPOT analyses, as reported earlier . The membranes were read by an independent agency (Zellnet Consulting Inc., New York, NY, USA) using the KS-ELISPOT automatic system (Carl Zeiss, Inc., Thornwood, NY, USA) for quantitative analyses of the number of IFN-γ spot forming cells (SFC) for 105 input PBMC. Responses were considered positive, according to criteria described in the literature , which is a minimum of five SFC per well and at least double the number obtained in cells cultured in the medium.
2.5. Cytokine Analysis by Cytokine Bead Array (CBA)
Single cell suspensions of PBMC from the immunized monkeys were cultured at a density of 1 × 105 per mL with or without the HIV-1 envelope peptide mixture and cell-free heat-inactivated SHI to detect antigen-specific cytokine production. Culture supernatants were collected 36 h after incubation, and the level of cytokines (IL-2, IL-4, IL-6, IL-10, IL-12p70, IFN-, and TNF-) was determined by cytometric bead array (CBA) kit (Lincoplex multiple cytokine assay, Millipore), according to manufacturer’s instructions. Antigen-specific cytokine production was measured as the cytokine concentration in culture supernatants of antigen-stimulated cells subtracting that without antigen.
2.6. Intracellular Cytokine Analyses
The PBMC along with lamina propria lymphocytes (LPL) isolated from the colon biopsies as previously described , were used for the analyses of antigen-specific intracellular cytokine production using the following antihuman monoclonal antibodies that cross-react with rhesus macaques: CD3 (clone SP34-2, PE-Cy7-labeled), CD8a (clone RPA-T8, Alexa 700-labeled), CD28 (clone L293, PerCP-Cy5.5-labeled), CD95 (clone DX2, APC-labeled), and IFN- (clone B27, FITC-labeled; all from BD Biosciences, San Jose, Calif, USA), CD4 (clone OKT4, Pacific blue-labeled; eBioScience, San Diego, Calif, USA), and Aqua (live/dead staining kit) from Invitrogen (Carlsbad, Calif, USA) to detect dead cells. The CD4+ and CD8+ T cells that produce IFN- in response to stimulation with various reagents were analyzed by the standard intracellular cytokine assay procedure, as previously described . Samples were collected on a three-laser CYAN ADP instrument (Dako Cytomation, Glostrup, Denmark) and analyzed using FloJo software (Tree Star, Ashland, OR). For data acquiring and analyzing, CD3+CD8+ or CD3+CD4+ T cells initially gated from live lymphocytes were further gated for CD95 memory phenotype. The gated CD4+ or CD8+ memory T cells were then analyzed for positive staining of IFN.
3. Results and Discussion
We used nonhuman primates to evaluate the translational potential for the chemokine-fusion strategy in the development of a novel HIV vaccine. Two macaques immunized with the plasmid DNA encoding MCP3-gp120 fusions demonstrated virus-reactive T-cell immunity at week 12, evidenced by the proliferation of T cells (Figure 1(a)) and IFN- producing cells in response to in vitro stimulation with heat-inactivated SHI (Figure 1(b)). Peptide-cocktail vaccine boosted the viral-reactive T-cell immunity, as evidenced by the significant elevation of IFN- producing cells in response to the heat-inactivated SHI in one of the two monkeys (Figure 1(b) #J160). The peptide-cocktail-specific response was readily detected after peptide boost, confirming the immunogenicity of the peptide-cocktail vaccine (Figure 1(c)). The macaque (#J8) that was weakly responsive to the peptide boost (Figure 1(b) #J8) also showed a low magnitude of peptide-cocktail-specific systemic cellular responses (Figure 1(c)). PBMC cultured with medium or treated with irrelevant human papilloma virus peptide failed to show positive responses (data not shown). We were unable to detect antibody responses, either by neutralization assay or by Western blot (data not shown).
To further investigate changes in the DNA vaccine-induced microenvironment that may facilitate the development of memory immunity, we monitored virus-reactive, PBMC cytokine induction throughout the entire prime-boost schedule. Strikingly, among a panel of cytokines including IL-2, IL-4, IL-6, IL-10, IL-12p70, IFN-, and TNF-α, production of IL-6 was found to be significantly increased upon initial vaccination with MCP-3-fused gp120 plasmid DNA. Of interest, immune cells harvested from the monkey #J160 during the boost period (W32–39) were considerably more active in producing IL-6, compared with PBMC collected from the macaque #J8 (Figure 1(d)).
We analyzed colon biopsy samples collected from the macaques one year after the final peptide-cocktail boost. During this year-long rest period the two vaccinated macaques received no further treatment. Surprisingly, antigen-specific CD4 and CD8 memory T cells were detected in lamina propria lymphocytes (LPL) isolated from the colon, suggesting long-term mucosal immunity. Specifically, after in vitro stimulation with the peptide-mix, subsets of IFN--producing CD3+CD4+CD95+ and CD3+CD8+CD95+ T cells were readily detected in both vaccinated macaques (Figure 2). The memory T cell response was found only in LPL samples, but not in PBMC (Figure 2). These results suggest that the immunization regimen induced mucosal memory cellular immune responses, which likely resulted from directly delivering viral antigen to the gastrointestinal mucosa by nasogastric administration of the peptide-cocktail.
Growing evidence has emphasized the central role of cellular immunity in the control of HIV infection. For example, the prevalence of virus-specific cytotoxic T cells has been associated with reduced viral RNA load and delayed clinical progression of the disease . In nonhuman primate models, depletion of CD8+ T lymphocytes resulted in marked viral replication in chronically infected animals . It is thus important to focus development of HIV vaccines that generate cellular immunity for therapeutic benefit. In this pilot study, we observed that the MCP3-fused gp120 DNA vaccine elicited the viral-reactive T-cell immunity in rhesus macaques that were vaccinated with as little as 20 g of plasmid DNA by gene gun injection. Although the individual response in terms of immunity potency was not robust, the immunogenicity of MCP3-gp120 fusions DNA vaccine in a nonhuman primate model was supported from the data obtained. Thus, future studies are warranted to confirm and extend the data from the proof-of-principle study employing bigger cohort of animals combined with determining protective efficacy against viral challenge. Furthermore, optimizing DNA delivery may also help to enhance the immunogenicity of the vaccine strategy. For example, we currently developed an immune potentiating strategy by inducing a sterile inflammation at vaccination sites, which significantly potentiated DNA vaccine-induced adaptive immunity . Nevertheless, the take-home message that MCP3-gp120 DNA vaccine induced T-cell immunity in macaques provides us with a rationale to further optimize the chemokine-fusion strategy for designing the next generation of HIV vaccines.
In contrast to activation of T-cell immunity, the fusion vaccine failed to induce antibody response. This may imply that antigen cross-presentation mechanism was predominantly responsible for the observed adaptive immunity. A striking feature of the chemokine fusion strategy is its receptor-mediated endocytosis that facilitates loading antigens to the MHC Class I pathway and thus polarizes Th1 response . Accordingly, we also observed in mice that chemokine-chicken ovalbumin fusion vaccine stimulated expansion of adoptively transferred antigen-specific CD8+ (OT-I), but not CD4+ (OT-II) T cells (unpublished data).
Mucosal entry is a major route of HIV infection. A recent clinical study suggests that blocking mucosal viral transmission would be critical to the prevention of systemic spread of HIV . The local mucosal immunity brings an additional beneficial influence to disease control. Therefore, an ideal HIV vaccine should be designed to activate both systemic and local immune responses. Our current study showed that nasogastric administration of multivalent antigen peptides not only boosted the genetic fusion-primed T cell immunity, but also elicited mucosal immunity. The antigen-specific, long-lasting T cell immunity was readily detected a year later after final vaccination, which renders our prime-boost strategy with an extra advantage in the aspect of prophylactic value.
Cytokines produced in the microenvironment may be mechanistically associated with the elicited immune response. Of particular interest in the current study was the significant increase in IL-6 upon vaccination with chemokine-fused gp120 plasmid DNA. This T-cell—derived cytokine was initially identified as a B-cell growth and differentiation factor  and was subsequently discovered to have a variety of biological activities, such as stimulating differentiation of myeloid precursors, activating T cells by enhancing IL-2 responsiveness, and regulating acute phase reaction [21–23]. The stimulatory function of IL-6 on diverse immune cells renders this cytokine a potential immune adjuvant in the development of adaptive immune response. The current study does not allow us to differentiate the mechanism that caused the production of IL-6. Since IL-6 is not constitutively produced by T cells, rather it is the consequence of tissue damage as seen in the case of viral or bacterial infection, we speculate that the viral gp120 protein component in the fusion construct of the DNA vaccine might be the stimulator for IL-6 production. Regardless of the underlining mechanism, our observation that sustained IL-6 production was correlated with vaccine boosting suggests a potential role of this cytokine in the maintenance of long-term memory immunity.
Future studies exploring the use of the chemokine-fusion strategy to develop vaccines targeting other HIV antigens including pol and gag gene products may be worthwhile. It has been reported that multivalent vaccines demonstrated superior antiviral effect over single antigen-derived vaccines . Combined with more efficient vaccinia viral vectors , we expect that DNA vaccines encoding multivalent HIV antigens fused with chemokines would be promising candidates for HIV vaccines.
The authors declare no competing financial interests.
H. Qin and P. N. Nehete equally contributed to the work. We thank Dr. D. Montefiori (Duke University Medical Center, Durham, NC) for the support in performing neutralizing antibody studies, and Dr. Ashok Chopra (The University of Texas Medical Branch, Galveston, TX) for providing the purified preparation of the mutant cholera toxin, CT. This work was supported by a translational research grant from Leukemia and Lymphoma Society (LWK), RO1 (AI 426969) and R21(AI 065402) grants from NIAID (KJS).
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