趋化因子受体:与HIV-1和病毒编码趋化因子的相互作用

Silvano Sozzani , Paola Allavena , Annunciata Vecchi , Jo Van Damme , Alberto Mantovani
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引用次数: 6

摘要

趋化因子是一个蛋白质超家族,在免疫和炎症反应以及病毒感染中发挥核心作用。大约有50种不同的趋化因子被分为四个亚家族,CXC, CC, C和CX3C。趋化因子受体可作为人类免疫缺陷病毒(HIV)-1感染的进入/融合共受体,细胞因子对受体表达的调节可能与病毒感染有关。趋化因子的翻译后加工可以深刻地影响它们与受体的相互作用。丝氨酸蛋白酶CD26/二肽基肽酶IV (CD26/DPP IV)可去除几种趋化因子中nh2末端的二肽,并深刻影响其生物活性。卡波西肉瘤(KS)相关疱疹病毒8编码三种与CC趋化因子MIP簇同源的趋化因子样蛋白。这些病毒趋化因子对某些趋化因子受体具有部分激动剂活性,可能具有受体拮抗剂的功能。这种生物活性可能代表了病毒开发的一种策略,以破坏免疫,损害有效抗病毒免疫反应的产生。
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Chemokine receptors: interaction with HIV-1 and viral-encoded chemokines

Chemokines are a superfamily of proteins that play a central role in immune and inflammatory reactions and in viral infections. About 50 different chemokines divided in four subfamilies are known, CXC, CC, C, and CX3C. Chemokine receptors can function as entry/fusion co-receptors for human immunodeficiency virus (HIV)-1 infection, and regulation of receptor expression by cytokines may be relevant for viral infection. Posttranslational processing of chemokines can profoundly affect their interaction with receptors. The serine protease CD26/dipeptidyl-peptidase IV (CD26/DPP IV) removes NH2-terminal dipeptides from several chemokines and profoundly affect their biological activity. Kaposi's sarcoma (KS)-associated herpes virus 8 encodes for three chemokine-like proteins that show homology with MIP cluster of CC chemokines. These viral chemokines possess a partial agonist activity for certain chemokine receptors and may function as receptor antagonists. This biological activity could represent a strategy developed by the virus to subvert immunity impairing the generation of an effective anti-viral immune response.

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