hiv编码蛋白在心血管疾病中的作用

IF 4.7 2区 生物学 Q2 CELL BIOLOGY
Laszlo Kovacs, Beryl N Khakina, Eric J Belin de Chantemèle
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引用次数: 0

摘要

由于抗逆转录病毒联合治疗(cART)的疗效,一度被认为是绝症的人类免疫缺陷病毒(HIV)感染已转变为一种慢性、可控制的疾病。因此,机会性感染的死亡率大幅下降,心血管疾病现在成为艾滋病毒感染者死亡的主要原因。与吸烟、血脂异常、代谢综合征和抗逆转录病毒联合治疗(cART)等传统危险因素一起,hiv编码蛋白已成为心血管病理的直接病因。这些病毒蛋白通过导致内皮细胞激活、慢性炎症、氧化应激和血管重塑的机制发挥致病作用。虽然许多研究已经调查了这种病毒蛋白对培养细胞的直接影响,但所报道的改变的病理生理相关性通常仍有待在体内环境中建立。这篇小型综述提供了这些蛋白在hiv相关心血管(CV)并发症中的作用的简要概述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of HIV-encoded proteins in cardiovascular disease.

Thanks to the efficacy of combination antiretroviral therapy (cART), human immunodeficiency virus (HIV) infection, once considered a terminal diagnosis, has transformed into a chronic, manageable condition. Consequently, mortality from opportunistic infections has significantly declined, with cardiovascular disease now emerging as the leading cause of death among people living with HIV (PLWH). Along with traditional risk factors like smoking, dyslipidemia, metabolic syndrome, and combination antiretroviral therapy (cART), HIV-encoded proteins have emerged as direct etiologies of cardiovascular pathology. These viral proteins have been shown to exert pathogenic effects through mechanisms that result in endothelial activation, chronic inflammation, oxidative stress, and vascular remodeling. Although many studies have investigated the direct effects of these viral proteins on cells in culture, the pathophysiological relevance of the alterations reported often remains to be established in an in vivo setting. This mini-review provides a brief overview of the role of these proteins in HIV-related cardiovascular (CV) complications.

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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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