Jones Norman G, DeCamp Allan, Gilbert Peter, Peterson Michael L, Gurwith Marc, Cao Huyen
California Department of Public Health, Richmond, CA 94804, United States.
Vaccine. 2009 Feb 11;27(7):1136-40. doi: 10.1016/j.vaccine.2008.11.071. Epub 2008 Dec 9.
Correlates of immune protection from HIV vaccines remain undefined. The first HIV vaccine efficacy trial in the US and Europe VAX004, was designed to assess whether rgp120 envelope subunits (AIDSVAX B/B, VaxGen) can induce partial or complete protection from HIV-1 infection. No effectiveness in the reduction of either the acquisition of infection or levels of plasma viremia after HIV infection was noted. We found evidence of vaccine-specific CD8+ T cells in volunteers who received the vaccine, regardless of behavioral risk. Surprisingly, the CD8-response is significantly higher in participants who would go on to contract HIV infection. These results suggest that AIDSVAX immunization may boost preexisting immune responses-due to pre-infection exposure, and a vaccine-induced immune profile may serve as a biological marker for HIV susceptibility.
HIV疫苗免疫保护的相关因素仍不明确。美国和欧洲的首个HIV疫苗疗效试验VAX004旨在评估重组gp120包膜亚单位(AIDSVAX B/B,VaxGen公司)能否诱导对HIV-1感染的部分或完全保护。未发现该疫苗在降低感染发生率或HIV感染后血浆病毒血症水平方面有任何效果。我们发现,无论行为风险如何,接种疫苗的志愿者体内存在疫苗特异性CD8+T细胞。令人惊讶的是,后续感染HIV的参与者的CD8反应明显更高。这些结果表明,AIDSVAX免疫接种可能会增强因感染前暴露而预先存在的免疫反应,并且疫苗诱导的免疫谱可能作为HIV易感性的生物学标志物。