Shi Yin, Wan Yanmin, Xu Jianqing
Bing Du Xue Bao. 2015 May;31(3):299-306.
Human immunodeficiency virus type 1 (HIV-1)-specific cytotoxic T lymphocytes (CTLs) play a critical role in the control of HIV-1 infection and replication. HIV-1 evades CTL mediated pressure through viral escape mutations within targeted CTLs epitopes or flanking regions, but this process is usually associated with a viral fitness cost. The mutated epitopes may weaken the level of the original CTL responses, however, the immune system holds potential to mount denovo responses towards those newly emerged epitopes. This article briefly summarizes recent research progress regarding the competition between HIV-1's escape mutations and host CTL responses.
1型人类免疫缺陷病毒(HIV-1)特异性细胞毒性T淋巴细胞(CTL)在控制HIV-1感染和复制中起关键作用。HIV-1通过靶向CTL表位或侧翼区域内的病毒逃逸突变来逃避CTL介导的压力,但这一过程通常伴随着病毒适应性代价。突变的表位可能会削弱原始CTL反应的水平,然而,免疫系统有潜力对那些新出现的表位产生重新反应。本文简要总结了关于HIV-1逃逸突变与宿主CTL反应之间竞争的最新研究进展。