Klute Susanne, Sparrer Konstantin M J
Institute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany.
Viruses. 2024 Mar 25;16(4):500. doi: 10.3390/v16040500.
Autophagy has emerged as an integral part of the antiviral innate immune defenses, targeting viruses or their components for lysosomal degradation. Thus, successful viruses, like pandemic human immunodeficiency virus 1 (HIV-1), evolved strategies to counteract or even exploit autophagy for efficient replication. Here, we provide an overview of the intricate interplay between autophagy and HIV-1. We discuss the impact of autophagy on HIV-1 replication and report in detail how HIV-1 manipulates autophagy in infected cells and beyond. We also highlight tissue and cell-type specifics in the interplay between autophagy and HIV-1. In addition, we weigh exogenous modulation of autophagy as a putative double-edged sword against HIV-1 and discuss potential implications for future antiretroviral therapy and curative approaches. Taken together, we consider both antiviral and proviral roles of autophagy to illustrate the ambivalent role of autophagy in HIV-1 pathogenesis and therapy.
自噬已成为抗病毒固有免疫防御的一个组成部分,它将病毒或其成分靶向溶酶体进行降解。因此,像大流行的人类免疫缺陷病毒1型(HIV-1)这样成功的病毒,进化出了对抗甚至利用自噬以实现高效复制的策略。在此,我们概述自噬与HIV-1之间复杂的相互作用。我们讨论自噬对HIV-1复制的影响,并详细报告HIV-1如何在感染细胞及其他情况下操纵自噬。我们还强调了自噬与HIV-1相互作用中的组织和细胞类型特异性。此外,我们权衡了自噬的外源性调节作为对抗HIV-1的一把双刃剑,并讨论了其对未来抗逆转录病毒治疗和治愈方法的潜在影响。综上所述,我们考虑自噬的抗病毒和前病毒作用,以说明自噬在HIV-1发病机制和治疗中的矛盾作用。