Belyakov Igor M, Ahlers Jeffrey D, Berzofsky Jay A
Molecular Immunogenetics and Vaccine Research, Section, Vaccine Branch, CCR, NCI, NIH, Bethesda, MD 20892, USA.
Expert Rev Vaccines. 2004 Aug;3(4 Suppl):S65-73. doi: 10.1586/14760584.3.4.s65.
Natural transmission of HIV occurs through mucosal surfaces. New information in immunology, virology and vaccinology has emerged regarding strategies for development of new mucosal vaccines against HIV. The intestinal mucosa represents a major site of HIV replication and amplification, and the initial site of CD4+ T-cell depletion. Local mucosal CD8+ cytotoxic T-lymphocytes (CTLs) and mucosal antibody can control AIDS virus replication within local tissues prior to systemic dissemination and can be more effective than a systemic immune response. Mucosal HIV vaccine delivery should be considered among the most effective immunization routes in the induction of mucosal antibody and CD8+ CTLs and protection against mucosal infection. New mucosal vaccine strategies, such as prime-boost, using a new generation of mucosal adjuvants, a synergistic combination of cytokines, chemokines, costimulatory molecules, CpG oligodeoxynucleotides, and targeting lymph nodes which drain mucosal sites, show promise to improve the efficacy of mucosal vaccines.
HIV的自然传播通过黏膜表面发生。关于开发新型抗HIV黏膜疫苗的策略,免疫学、病毒学和疫苗学领域已出现了新信息。肠道黏膜是HIV复制和扩增的主要部位,也是CD4+ T细胞耗竭的起始部位。局部黏膜CD8+ 细胞毒性T淋巴细胞(CTL)和黏膜抗体可在全身扩散之前控制局部组织内的艾滋病病毒复制,且比全身免疫反应更有效。黏膜HIV疫苗接种应被视为诱导黏膜抗体和CD8+ CTL以及预防黏膜感染的最有效免疫途径之一。新型黏膜疫苗策略,如采用新一代黏膜佐剂的初免-加强免疫、细胞因子、趋化因子、共刺激分子、CpG寡脱氧核苷酸的协同组合以及靶向引流黏膜部位的淋巴结,有望提高黏膜疫苗的效力。