Wikramaratna Paul S, Lourenço José, Klenerman Paul, Pybus Oliver G, Gupta Sunetra
Department of Zoology, University of Oxford, Oxford OX1 3PS, UK.
Nuffield Department of Clinical Medicine, University of Oxford, Oxford OX3 7BN, UK.
Philos Trans R Soc Lond B Biol Sci. 2015 Aug 19;370(1675). doi: 10.1098/rstb.2014.0290.
Despite substantial advances in our knowledge of immune responses against HIV-1 and of its evolution within the host, it remains unclear why control of the virus eventually breaks down. Here, we present a new theoretical framework for the infection dynamics of HIV-1 that combines antibody and CD8(+) T-cell responses, notably taking into account their different lifespans. Several apparent paradoxes in HIV pathogenesis and genetics of host susceptibility can be reconciled within this framework by assigning a crucial role to antibody responses in the control of viraemia. We argue that, although escape from or progressive loss of quality of CD8(+) T-cell responses can accelerate disease progression, the underlying cause of the breakdown of virus control is the loss of antibody induction due to depletion of CD4(+) T cells. Furthermore, strong antibody responses can prevent CD8(+) T-cell escape from occurring for an extended period, even in the presence of highly efficacious CD8(+) T-cell responses.
尽管我们在了解针对HIV-1的免疫反应及其在宿主体内的演变方面取得了重大进展,但病毒控制最终为何会失效仍不清楚。在此,我们提出了一个针对HIV-1感染动态的新理论框架,该框架结合了抗体和CD8(+) T细胞反应,尤其考虑到了它们不同的寿命。通过赋予抗体反应在控制病毒血症中关键作用,HIV发病机制和宿主易感性遗传学中的几个明显矛盾可以在这个框架内得到调和。我们认为,虽然CD8(+) T细胞反应的逃逸或质量的逐渐丧失会加速疾病进展,但病毒控制失效的根本原因是由于CD4(+) T细胞耗竭导致抗体诱导的丧失。此外,即使存在高效的CD8(+) T细胞反应,强烈的抗体反应也可以在较长时间内阻止CD8(+) T细胞逃逸的发生。