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巨噬细胞:HIV-1感染中的一个治疗靶点。

The macrophage: a therapeutic target in HIV-1 infection.

作者信息

Kumar Amit, Herbein Georges

机构信息

Department of Virology, UPRES EA4266 Pathogens & Inflammation, University of Franche-Comte, SFR FED 4234, F-25030 Besançon, France.

Department of Virology, UPRES EA4266 Pathogens & Inflammation, University of Franche-Comte, SFR FED 4234, F-25030 Besançon, France ; Department of Virology, Hôpital Saint-Jacques, CHRU Besançon, 2 place Saint-Jacques, F-25030 Besançon cedex, France.

出版信息

Mol Cell Ther. 2014 Apr 2;2:10. doi: 10.1186/2052-8426-2-10. eCollection 2014.

Abstract

Human immunodeficiency virus (HIV) is still a serious global health concern responsible for more than 25 million deaths in last three decades. More than 34 million people are living with HIV infection. Macrophages and CD4+ T cells are the principal targets of HIV-1. The pathogenesis of HIV-1 takes different routes in macrophages and CD4+ T cells. Macrophages are resistant to the cytopathic effect of HIV-1 and produce virus for longer periods of time. In addition, macrophages being present in every organ system thus can disseminate virus to the different anatomical sites leading to the formation of viral sanctuaries. Complete cure of HIV-1 needs better understanding of viral pathogenesis in these reservoirs and implementation of knowledge into robust therapeutic products. In this review we will focus on the unique relationship between HIV-1 and macrophages. Furthermore, we will describe how successful antiretroviral therapy (ART) is in suppressing HIV and novel molecular and cellular strategies against HIV-1 in macrophages.

摘要

人类免疫缺陷病毒(HIV)仍然是一个严重的全球健康问题,在过去三十年中导致了超过2500万人死亡。超过3400万人感染了HIV。巨噬细胞和CD4+ T细胞是HIV-1的主要靶细胞。HIV-1在巨噬细胞和CD4+ T细胞中的发病机制有所不同。巨噬细胞对HIV-1的细胞病变效应具有抗性,并能长时间产生病毒。此外,巨噬细胞存在于每个器官系统中,因此可以将病毒传播到不同的解剖部位,导致病毒储存库的形成。彻底治愈HIV-1需要更好地了解这些储存库中的病毒发病机制,并将相关知识应用于强大的治疗产品中。在这篇综述中,我们将重点关注HIV-1与巨噬细胞之间的独特关系。此外,我们将描述成功的抗逆转录病毒疗法(ART)在抑制HIV方面的作用,以及针对巨噬细胞中HIV-1的新型分子和细胞策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/249c/4452058/0b39624bf2bb/40591_2013_13_Fig1_HTML.jpg

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