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跨膜蛋白会导致由人类免疫缺陷病毒1型(HIV-1)和其他逆转录病毒引起的免疫缺陷。

The transmembrane proteins contribute to immunodeficiencies induced by HIV-1 and other retroviruses.

作者信息

Denner Joachim

机构信息

Robert Koch Institute, Berlin, Germany.

出版信息

AIDS. 2014 May 15;28(8):1081-90. doi: 10.1097/QAD.0000000000000195.

Abstract

Many microorganisms including retroviruses suppress the immune system of the infected host in order to maintain infection. Unfortunately, it is still unclear how retroviruses induce immunosuppression. There is increasing evidence of a common mechanism based on their transmembrane envelope proteins. This review therefore summarizes evidence of the involvement of the transmembrane envelope proteins in the immunopathogenesis of different retroviruses including HIV-1. Mutations in the immunosuppressive (isu) domain of the transmembrane envelope protein of several retroviruses abrogate the immunosuppressive activities in vitro and in vivo. Most importantly, virus sequences with such abrogating mutations were never found in HIV-1-infected individuals despite the fact that the mutated viruses are replication-competent. However, there is also evidence for additional, perhaps even divergent, strategies for each retrovirus. For example, in contrast to many other retroviruses, the HIV directly interacts with immune cells and infects them. In addition, HIV uses several accessory proteins to evade the immune response. Furthermore, the possible contribution of the transmembrane envelope proteins of endogenous retroviruses to immunosuppression when expressed on tumor cells or in the placenta is analyzed.

摘要

包括逆转录病毒在内的许多微生物会抑制受感染宿主的免疫系统以维持感染。不幸的是,逆转录病毒如何诱导免疫抑制仍不清楚。越来越多的证据表明存在一种基于其跨膜包膜蛋白的共同机制。因此,本综述总结了跨膜包膜蛋白参与包括HIV-1在内的不同逆转录病毒免疫发病机制的证据。几种逆转录病毒跨膜包膜蛋白的免疫抑制(isu)结构域中的突变在体外和体内消除了免疫抑制活性。最重要的是,尽管突变病毒具有复制能力,但在HIV-1感染个体中从未发现具有这种消除突变的病毒序列。然而,也有证据表明每种逆转录病毒还有其他甚至可能不同的策略。例如,与许多其他逆转录病毒不同,HIV直接与免疫细胞相互作用并感染它们。此外,HIV利用几种辅助蛋白来逃避免疫反应。此外,还分析了内源性逆转录病毒的跨膜包膜蛋白在肿瘤细胞或胎盘中表达时对免疫抑制的可能作用。

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