Critical issues in mucosal immunity for HIV-1 vaccine development
- PMID: 18468671
- PMCID: PMC3014573
- DOI: 10.1016/j.jaci.2008.03.036
Critical issues in mucosal immunity for HIV-1 vaccine development
Abstract
Development of a safe and effective vaccine for HIV-1 infection is a critical global priority. However, the nature of host-virus interactions that lead to early immunosuppression and CD4 depletion, HIV-1 diversity, and the inability of the immune system to eliminate the latently infected CD4 pool of cells has to date thwarted successful vaccine development. Moreover, both the initial antibody-inducing vaccine (protein envelope gp120) and cell-mediated vaccine (recombinant adenovirus containing HIV-1 genes) strategies have failed in efficacy trials, and the latter cell-mediated vaccine appeared to have caused enhanced HIV-1 acquisition. Thus basic and translational research to understand why current vaccines have failed and elucidation of new mechanisms of virus control at mucosal surfaces is essential for eventual successful development of a preventive HIV-1 vaccine.
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References
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- Klausner RD, Fauci AS, Corey L, Nabel GJ, Gayle H, Berkley S, et al. Medicine. The need for a global HIV vaccine enterprise. Science. 2003;300:2036–9. - PubMed
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- Shattock RJ, Haynes BF, Pulendran B, Flores J, Esparza J on behalf of a Working Group convened by the Global HIV Vaccine Enterprise. Improving defences at the portal of entry: Mucosal and innate immunity (Summary Report from a Global HIV Vaccine Enterprise Working Group) PLoS Med. 2008;5:e81. - PMC - PubMed
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