Tomaras G D, Greenberg M L
Department of Surgery, Center for AIDS Research, Duke University Medical Center, Durham, NC 27710, USA.
Front Biosci. 2001 Mar 1;6:D575-98. doi: 10.2741/tomaras.
The development of cellular immune responses in primary human immunodeficiency virus type-1 (HIV-1) infection is accompanied by a dramatic decrease in plasma viremia and resolution of the acute clinical syndrome. The full nature of the immunological response and its consequences on HIV pathogenesis is still largely a mystery, but significant progress has been achieved in the characterization of some of the players involved. Several studies indicate that noncytolytic HIV suppression by CD8+ T lymphocytes may be inversely associated with viral load suggesting that this antiviral activity is important in host control of HIV replication. This review focuses on this antiviral activity by CD8+ T lymphocytes, which is distinct from that activity elicited by some cytolytic CD8+ T lymphocytes (CTLs).
在原发性人类免疫缺陷病毒1型(HIV-1)感染中,细胞免疫反应的发展伴随着血浆病毒血症的显著下降和急性临床综合征的消退。免疫反应的全貌及其对HIV发病机制的影响在很大程度上仍是个谜,但在对一些相关参与者的特征描述方面已取得了重大进展。多项研究表明,CD8+ T淋巴细胞对HIV的非细胞溶解性抑制可能与病毒载量呈负相关,这表明这种抗病毒活性在宿主控制HIV复制中很重要。本综述重点关注CD8+ T淋巴细胞的这种抗病毒活性,它不同于某些细胞溶解性CD8+ T淋巴细胞(CTL)所引发的活性。