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抗逆转录病毒药物疗法改变了1型人类免疫缺陷病毒特异性T细胞反应的概况,并将免疫显性细胞毒性T淋巴细胞反应从Gag转移到Pol。

Antiretroviral drug therapy alters the profile of human immunodeficiency virus type 1-specific T-cell responses and shifts the immunodominant cytotoxic T-lymphocyte response from Gag to Pol.

作者信息

Karlsson A C, Chapman J M, Heiken B D, Hoh R, Kallas E G, Martin J N, Hecht F M, Deeks S G, Nixon D F

机构信息

Gladstone Institute of Virology and Immunology, University of California, San Francisco, California 94141, USA.

出版信息

J Virol. 2007 Oct;81(20):11543-8. doi: 10.1128/JVI.00779-07. Epub 2007 Aug 1.

Abstract

Antiretroviral drug therapy and cytotoxic T lymphocytes (CTL) both exert selective pressures on human immunodeficiency virus type 1, which influence viral evolution. Compared to chronically infected, antiretroviral-untreated patients, most chronically infected, treated patients with detectable viremia lack a cellular immune response against the Gag 77-85(SL9) epitope but show a new immunodominant response against an epitope in protease PR 76-84. Hence, mutations induced by antiretroviral therapy likely alter the profile of epitopes presented to T cells and thus the direction of the response. The consequences of dual pressures from treatment and CTL need to be considered in monitoring of drug therapy.

摘要

抗逆转录病毒药物疗法和细胞毒性T淋巴细胞(CTL)都会对1型人类免疫缺陷病毒施加选择性压力,从而影响病毒的进化。与未经抗逆转录病毒治疗的慢性感染患者相比,大多数接受治疗且病毒血症可检测到的慢性感染患者缺乏针对Gag 77-85(SL9)表位的细胞免疫反应,但对蛋白酶PR 76-84中的一个表位表现出新的免疫显性反应。因此,抗逆转录病毒疗法诱导的突变可能会改变呈递给T细胞的表位谱,进而改变免疫反应的方向。在药物治疗监测中需要考虑治疗和CTL双重压力的后果。

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