Shiver John W, Emini Emilio A
Vaccine Research, Merck Research Laboratories, West Point, Pennsylvania 19486, USA.
Annu Rev Med. 2004;55:355-72. doi: 10.1146/annurev.med.55.091902.104344.
An increasing body of evidence suggests that a vaccine that elicits anti-HIV-1 cellular immunity could provide the basis for an effective AIDS vaccine. Comparative immunization experiments testing a variety of vaccine approaches have demonstrated that replication-incompetent adenovirus vectors are an effective means for eliciting cytotoxic T-lymphocyte (CTL) immune responses against HIV-1 antigens. These immune responses effectively control viremia in nonhuman primates following challenge with simian AIDS viruses. Such data, coupled with epidemiology studies that identify HIV-1 gag, pol, and nef as the best antigens for broadly directed cellular immune responses, provide guidance for the development of a potential AIDS vaccine.
越来越多的证据表明,一种能引发抗HIV-1细胞免疫的疫苗可为有效的艾滋病疫苗奠定基础。对多种疫苗方法进行测试的比较免疫实验表明,无复制能力的腺病毒载体是引发针对HIV-1抗原的细胞毒性T淋巴细胞(CTL)免疫反应的有效手段。在用猿类艾滋病病毒攻击后,这些免疫反应能有效控制非人灵长类动物的病毒血症。这些数据,再加上将HIV-1 gag、pol和nef确定为广泛定向细胞免疫反应最佳抗原的流行病学研究,为潜在艾滋病疫苗的研发提供了指导。