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作为特洛伊外泌体的HIV:免疫悖论得到解释了吗?

HIV As Trojan Exosome: Immunological Paradox Explained?

作者信息

Hildreth James E K

机构信息

Department of Internal Medicine, School of Medicine, Meharry Medical College, Nashville, TN, United States.

出版信息

Front Immunol. 2017 Dec 1;8:1715. doi: 10.3389/fimmu.2017.01715. eCollection 2017.

Abstract

The HIV pandemic is still a major global challenge, despite the widespread availability of antiretroviral drugs. An effective vaccine would be the ideal approach to bringing the pandemic to an end. However, developing an effective HIV vaccine has proven to be an elusive goal. Three major human HIV vaccine trials revealed a strong trend toward greater risk of infection among vaccine recipients versus controls. A similar observation was made in a macaque SIV vaccine study. The mechanism explaining this phenomenon is not known. Here, a model is presented that may explain the troubling results of vaccine studies and an immunological paradox of HIV pathogenesis: preferential infection of HIV-specific T cells. The central hypothesis of this perspective is that as "Trojan exosomes" HIV particles can directly activate HIV-specific T cells enhancing their susceptibility to infection. Understanding the biology of HIV as an exosome may provide insights that enable novel approaches to vaccine development.

摘要

尽管抗逆转录病毒药物已广泛可得,但艾滋病疫情仍是一项重大的全球挑战。有效的疫苗将是终结这一疫情的理想方法。然而,事实证明,研发一种有效的艾滋病疫苗是一个难以实现的目标。三项主要的人类艾滋病疫苗试验显示,与对照组相比,疫苗接种者感染风险有大幅增加的强烈趋势。在一项猕猴猴免疫缺陷病毒(SIV)疫苗研究中也有类似的观察结果。解释这一现象的机制尚不清楚。在此,我们提出一个模型,该模型或许可以解释疫苗研究中令人困扰的结果以及艾滋病发病机制中的一个免疫悖论:艾滋病特异性T细胞的优先感染。这一观点的核心假设是,作为“特洛伊外泌体”,艾滋病病毒颗粒可直接激活艾滋病特异性T细胞,增强其感染易感性。将艾滋病病毒理解为外泌体的生物学特性,可能会为疫苗研发的新方法提供思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/376a/5716971/2dd88d86cc81/fimmu-08-01715-g001.jpg

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