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MHC-I基因型与HIV/SIV感染疾病进展的关联

Association of MHC-I genotypes with disease progression in HIV/SIV infections.

作者信息

Nomura Takushi, Matano Tetsuro

机构信息

AIDS Research Center, National Institute of Infectious Diseases, Tokyo, Japan.

出版信息

Front Microbiol. 2012 Jun 29;3:234. doi: 10.3389/fmicb.2012.00234. eCollection 2012.

Abstract

Virus-specific cytotoxic T lymphocytes (CTLs) are major effectors in acquired immune responses against viral infection. Virus-specific CTLs recognize specific viral peptides presented by major histocompatibility complex class-I (MHC-I) on the surface of virus-infected target cells via their T cell receptor (TCR) and eliminate target cells by both direct and indirect mechanisms. In human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) infections, host immune responses fail to contain the virus and allow persistent viral replication, leading to AIDS progression. CTL responses exert strong suppressive pressure on HIV/SIV replication and cumulative studies have indicated association of HLA/MHC-I genotypes with rapid or slow AIDS progression.

摘要

病毒特异性细胞毒性T淋巴细胞(CTLs)是针对病毒感染的获得性免疫反应中的主要效应细胞。病毒特异性CTLs通过其T细胞受体(TCR)识别病毒感染靶细胞表面由主要组织相容性复合体I类(MHC-I)呈递的特定病毒肽,并通过直接和间接机制清除靶细胞。在人类免疫缺陷病毒(HIV)和猴免疫缺陷病毒(SIV)感染中,宿主免疫反应无法控制病毒,导致病毒持续复制,进而导致艾滋病进展。CTL反应对HIV/SIV复制施加强大的抑制压力,累积研究表明HLA/MHC-I基因型与艾滋病快速或缓慢进展有关。

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