McElrath M J, Corey L, Greenberg P D, Matthews T J, Montefiori D C, Rowen L, Hood L, Mullins J I
Department of Medicine, University of Washington School of Medicine, Seattle 98195, USA.
Proc Natl Acad Sci U S A. 1996 Apr 30;93(9):3972-7. doi: 10.1073/pnas.93.9.3972.
With efforts underway to develop a preventive human immunodeficiency virus type 1 (HIV-1) vaccine, it remains unclear which immune responses are sufficient to protect against infection and whether prior HIV-1 immunity can alter the subsequent course of HIV-1 infection. We investigated these issues in the context of a volunteer who received six HIV-1LAI envelope immunizations and 10 weeks thereafter acquired HIV-1 infection through a high-risk sexual exposure. In contrast to nonvaccinated acutely infected individuals, anamnestic HIV-1-specific B- and T-cell responses appeared within 3 weeks in this individual, and neutralizing antibody preceded CD8+ cytotoxic responses. Despite an asymptomatic course and an initial low level of detectable infectious virus, a progressive CD4+ cell decline and dysfunction occurred within 2 years. Although vaccination elicited immunity to HIV-1 envelope, which was recalled upon HIV-1 exposure, it was insufficient to prevent infection and subsequent immunodeficiency.
随着开发预防1型人类免疫缺陷病毒(HIV-1)疫苗的工作正在进行,目前仍不清楚哪些免疫反应足以预防感染,以及先前的HIV-1免疫是否会改变随后的HIV-1感染进程。我们在一名志愿者的背景下研究了这些问题,该志愿者接受了6次HIV-1LAI包膜免疫接种,10周后通过高危性接触感染了HIV-1。与未接种疫苗的急性感染个体不同,该个体在3周内出现了记忆性HIV-1特异性B细胞和T细胞反应,中和抗体先于CD8+细胞毒性反应出现。尽管病程无症状且最初可检测到的感染性病毒水平较低,但在2年内仍出现了CD4+细胞的渐进性下降和功能障碍。虽然疫苗接种引发了对HIV-1包膜的免疫,在接触HIV-1时可被唤起,但这不足以预防感染和随后的免疫缺陷。