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树突状细胞与HIV特异性CD4+ T细胞:HIV抗原呈递、T细胞活化及病毒转移

Dendritic cells and HIV-specific CD4+ T cells: HIV antigen presentation, T-cell activation, and viral transfer.

作者信息

Moris Arnaud, Pajot Anthony, Blanchet Fabien, Guivel-Benhassine Florence, Salcedo Margarita, Schwartz Olivier

机构信息

Groupe Virus et Immunité, Unité de Recherche Associée (URA) Centre National de la Recherche Scientifique (CNRS) 1930, Paris, France.

出版信息

Blood. 2006 Sep 1;108(5):1643-51. doi: 10.1182/blood-2006-02-006361. Epub 2006 May 4.

Abstract

Human immunodeficiency virus (HIV)-specific CD4+ lymphocytes are preferentially infected in HIV-positive individuals. To study this preferential infection, we have derived several HIV-specific (HS) CD4+ clones. We show that in dendritic cells (DCs), HIV virion capture led to major histocompatibility complex class-II (MHC-II)-restricted viral antigen presentation and to activation of HS cells. In contrast, neither cell-free virions nor infected lymphocytes activated HS cells. In DCs, the dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin (DC-SIGN/CD209), which internalizes virions, promoted MHC-II presentation of HIV antigens. Activation of HS cells by HIV-exposed DCs triggered an efficient viral spread in lymphocytes. CD4+ clones with irrelevant antigenic specificities were not activated by HIV-exposed DCs and poorly supported viral replication under this setting. Our results unravel the mechanisms of MHC-II-restricted HIV antigen presentation by DCs and describe how HIV gains access to the very cells designed by the immune system to counteract this pathogen.

摘要

人类免疫缺陷病毒(HIV)特异性CD4+淋巴细胞在HIV阳性个体中优先被感染。为了研究这种优先感染,我们获得了几个HIV特异性(HS)CD4+克隆。我们发现,在树突状细胞(DC)中,HIV病毒体捕获导致主要组织相容性复合体II类(MHC-II)限制性病毒抗原呈递,并激活HS细胞。相比之下,游离病毒体和感染的淋巴细胞均未激活HS细胞。在DC中,内化病毒体的树突状细胞特异性细胞间黏附分子3结合非整合素(DC-SIGN/CD209)促进了HIV抗原的MHC-II呈递。暴露于HIV的DC激活HS细胞引发了淋巴细胞中高效的病毒传播。具有不相关抗原特异性的CD4+克隆未被暴露于HIV的DC激活,在此情况下对病毒复制的支持也很差。我们的结果揭示了DC进行MHC-II限制性HIV抗原呈递的机制,并描述了HIV如何进入免疫系统设计用来对抗这种病原体的细胞。

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