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Rev活性决定了HIV-1感染的原代T细胞对CTL杀伤的敏感性。

Rev activity determines sensitivity of HIV-1-infected primary T cells to CTL killing.

作者信息

Bobbitt Kevin R, Addo Marylyn M, Altfeld Marcus, Filzen Tracey, Onafuwa Adewunmi A, Walker Bruce D, Collins Kathleen L

机构信息

Department of Internal Medicine, The University of Michigan, Ann Arbor, MI 48109, USA.

出版信息

Immunity. 2003 Feb;18(2):289-99. doi: 10.1016/s1074-7613(03)00031-1.

Abstract

The HIV Nef protein is thought to promote HIV immune evasion by downmodulating MHC-I and protecting infected cells from CTL killing. In addition, we demonstrated that Rev, an HIV regulatory protein needed for expression of the HIV late genes, can influence CTL killing. When Rev activity level was reduced by virtue of amino acid alterations in the Rev protein sequence, infected cells were more resistant to anti-Gag and anti-Env CTL killing. A screen of primary viral isolates revealed that viruses derived from asymptomatic, infected people had lower Rev activity, lower Gag levels, and greater resistance to anti-Gag CTL killing. Thus, rev alleles with low activity may have a selective advantage in infected people with effective immune responses.

摘要

HIV Nef蛋白被认为通过下调主要组织相容性复合体I类分子(MHC-I)以及保护受感染细胞免受细胞毒性T淋巴细胞(CTL)杀伤来促进HIV免疫逃逸。此外,我们证明了Rev(一种HIV晚期基因表达所需的HIV调节蛋白)可影响CTL杀伤。当Rev蛋白序列中的氨基酸改变导致Rev活性水平降低时,受感染细胞对针对Gag和Env的CTL杀伤更具抗性。对原发性病毒分离株的筛选显示,来自无症状感染者的病毒具有较低的Rev活性、较低的Gag水平以及对针对Gag的CTL杀伤更强的抗性。因此,低活性的rev等位基因在具有有效免疫反应的感染者中可能具有选择优势。

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