Kramski Marit, Stratov Ivan, Kent Stephen J
Department of Microbiology and Immunology, The University of Melbourne, The Peter Doherty Institute of Infection and Immunity, Melbourne, Victoria, Australia.
AIDS. 2015 Jan 14;29(2):137-44. doi: 10.1097/QAD.0000000000000523.
There is growing interest in the role of anti-HIV antibody-dependent cellular cytotoxicity (ADCC) antibodies in the prevention and control of HIV infection. Passive transfer studies in macaques support a role for the Fc region of antibodies in assisting in the prevention of simian-human immunodeficiency virus (SHIV) infection. The Thai RV144 HIV-1 vaccine trial induced anti-HIV ADCC antibodies that may have played a role in the partial protection observed. Several observational studies support a role for ADCC antibodies in slowing HIV disease progression. However, HIV evolves to escape ADCC antibodies and chronic HIV infections causes dysfunction of effector cells such as natural killer (NK) cells that mediate the ADCC functions. Further, four recent studies show that the HIV-1 Vpu protein, by promoting release of virions, reduces the capacity of ADCC antibodies to recognize HIV-infected cells. The review dissects some of the recent research on HIV-specific ADCC antibodies and discusses mechanisms to further harness ADCC antibodies in the prevention and control of HIV infection.
抗HIV抗体依赖性细胞毒性(ADCC)抗体在HIV感染的预防和控制中的作用正受到越来越多的关注。在猕猴身上进行的被动转移研究支持抗体的Fc区域在协助预防猿猴-人类免疫缺陷病毒(SHIV)感染中发挥作用。泰国RV144 HIV-1疫苗试验诱导出了抗HIV ADCC抗体,这些抗体可能在观察到的部分保护作用中发挥了作用。几项观察性研究支持ADCC抗体在减缓HIV疾病进展中发挥作用。然而,HIV会发生进化以逃避ADCC抗体,并且慢性HIV感染会导致介导ADCC功能的效应细胞(如自然杀伤(NK)细胞)功能障碍。此外,最近的四项研究表明,HIV-1 Vpu蛋白通过促进病毒粒子的释放,降低了ADCC抗体识别HIV感染细胞的能力。这篇综述剖析了一些关于HIV特异性ADCC抗体的最新研究,并讨论了在HIV感染的预防和控制中进一步利用ADCC抗体的机制。