Department Emerging Pathogens and Vaccines, The John Curtin School of Medical Research, The Australian National University, Canberra, Australian Capital Territory, Australia.
Immunol Cell Biol. 2011 Mar;89(3):367-74. doi: 10.1038/icb.2010.118. Epub 2010 Oct 19.
Numerous human immunodeficiency virus (HIV)-1 vaccines have been developed over the last three decades, but to date an effective HIV-1 vaccine that can be used for prophylactic or therapeutic purposes in humans has not been identified. The failures and limited successes of HIV-1 vaccines have highlighted the gaps in our knowledge with regard to fundamental immunity against HIV-1 and have provided insights for vaccine strategies that may be implemented for designing more effective HIV-1 vaccines in the future. Recent studies have shown that robust mucosal immunity, high avidity and polyfunctional T cells, and broadly neutralizing antibodies are important factors governing the induction of protective immunity against HIV-1. Furthermore, optimization of vaccine delivery methods for DNA or live viral vector-based vaccines, elucidating the immune responses of individuals who remain resistant to HIV-1 infections and also understanding the core immune responses mediating protection against simian immunodeficiency viruses (SIV) and HIV-1 in animal models following vaccination, are key aspects to be regarded for designing more effective HIV-1 vaccines in the future.
在过去的三十年中,已经开发了许多人类免疫缺陷病毒 (HIV)-1 疫苗,但迄今为止,尚未发现可用于预防或治疗人类的有效 HIV-1 疫苗。HIV-1 疫苗的失败和有限成功突出表明,我们对针对 HIV-1 的基本免疫的了解存在差距,并为疫苗策略提供了见解,这些策略可能会在未来用于设计更有效的 HIV-1 疫苗。最近的研究表明,强大的粘膜免疫、高亲和力和多功能 T 细胞以及广泛中和抗体是控制诱导针对 HIV-1 的保护性免疫的重要因素。此外,优化针对 DNA 或活病毒载体疫苗的疫苗接种方法、阐明对 HIV-1 感染仍具有抵抗力的个体的免疫反应,以及了解在接种疫苗后动物模型中针对猴免疫缺陷病毒 (SIV) 和 HIV-1 进行保护的核心免疫反应,都是未来设计更有效的 HIV-1 疫苗需要考虑的关键方面。