Riley James L, Montaner Luis J
Department of Microbiology and Center for Cellular Immunotherapies, University of Pennsylvania, and.
HIV-1 Immunopathogenesis Laboratory, Wistar Institute, Philadelphia, Pennsylvania.
J Infect Dis. 2017 Mar 15;215(suppl_3):S160-S171. doi: 10.1093/infdis/jix002.
Effective clearance of virally infected cells requires the sequential activity of innate and adaptive immunity effectors. In human immunodeficiency virus (HIV) infection, naturally induced cell-mediated immune responses rarely eradicate infection. However, optimized immune responses could potentially be leveraged in HIV cure efforts if epitope escape and lack of sustained effector memory responses were to be addressed. Here we review leading HIV cure strategies that harness cell-mediated control against HIV in stably suppressed antiretroviral-treated subjects. We focus on strategies that may maximize target recognition and eradication by the sequential activation of a reconstituted immune system, together with delivery of optimal T-cell responses that can eliminate the reservoir and serve as means to maintain control of HIV spread in the absence of antiretroviral therapy (ART). As evidenced by the evolution of ART, we argue that a combination of immune-based strategies will be a superior path to cell-mediated HIV control and eradication. Available data from several human pilot trials already identify target strategies that may maximize antiviral pressure by joining innate and engineered T cell responses toward testing for sustained HIV remission and/or cure.
有效清除病毒感染细胞需要固有免疫和适应性免疫效应器的顺序性活动。在人类免疫缺陷病毒(HIV)感染中,自然诱导的细胞介导免疫反应很少能根除感染。然而,如果能够解决表位逃逸和缺乏持续效应记忆反应的问题,优化后的免疫反应可能会在HIV治愈研究中发挥作用。在此,我们综述了在抗逆转录病毒治疗稳定抑制的受试者中利用细胞介导的控制来对抗HIV的主要HIV治愈策略。我们关注的策略是,通过重组免疫系统的顺序激活,以及提供能够消除病毒储存库并在无抗逆转录病毒治疗(ART)的情况下维持对HIV传播控制的最佳T细胞反应,来最大化靶标识别和根除。正如ART的发展所证明的,我们认为基于免疫的策略组合将是实现细胞介导的HIV控制和根除的更优途径。来自几项人体试点试验的现有数据已经确定了一些靶向策略,这些策略可以通过结合固有免疫和工程化T细胞反应来最大化抗病毒压力,以测试是否能实现持续的HIV缓解和/或治愈。