Cytokine regulation of HIV expression.

Lymphokine research Pub Date : 1990-01-01
A S Fauci
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Abstract

Infection with the human immunodeficiency virus (HIV) is characterized by a long and variable asymptomatic phase followed by the development of the acquired immunodeficiency syndrome (AIDS) in a substantial proportion of individuals within 10 years. An understanding of the mechanism by which the infection progresses in vivo to an ultimate destruction of the immune system is essential to the design of rational approaches to anti-viral therapy, immune reconstitution, and vaccine development. To delineate these complex processes, we have established an in vitro model of latent or chronic HIV infection and have used this model to examine ways in which HIV replication can be upregulated. We have shown that cytokines are important mediators of HIV replication in chronically HIV-infected cells. Thus, the virus has incorporated itself into the human immune system and utilizes for its own propagation many of the cellular and molecular mechanisms which the immune system uses to maintain its homeostatic regulation. Studies in this area will not only shed important light on the immunopathogenesis of HIV, but will certainly lead to greater depth in our understanding of the normal function of the human immune system.

细胞因子调控HIV表达。
人类免疫缺陷病毒(HIV)感染的特点是一个漫长而多变的无症状阶段,随后在10年内发展为获得性免疫缺陷综合征(艾滋病)。了解感染在体内发展到最终破坏免疫系统的机制,对于设计合理的抗病毒治疗方法、免疫重建和疫苗开发至关重要。为了描述这些复杂的过程,我们建立了一个潜伏或慢性HIV感染的体外模型,并使用该模型来研究HIV复制上调的方式。我们已经证明细胞因子是慢性HIV感染细胞中HIV复制的重要介质。因此,病毒已将自身纳入人体免疫系统,并利用免疫系统用于维持其稳态调节的许多细胞和分子机制进行自身繁殖。这一领域的研究不仅将为HIV的免疫发病机制提供重要的线索,而且必将使我们对人类免疫系统的正常功能有更深入的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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