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CCL19 and CCR7 Expression Signaling Pathways and Adjuvant Functions in Viral Infection and Prevention

机译:CCL19和CCR7在病毒感染和预防中的表达信号通路和佐剂功能

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摘要

Chemokine (C–C motif) ligand 19 (CCL19) is a critical regulator of the induction of T cell activation, immune tolerance, and inflammatory responses during continuous immune surveillance, homeostasis, and development. Migration of CC-chemokine receptor 7 (CCR7)-expressing cells to secondary lymphoid organs is a crucial step in the onset of adaptive immunity, which is initiated by a complex interaction between CCR7 and its cognate ligands. Recent advances in knowledge regarding the response of the CCL19-CCR7 axis to viral infections have elucidated the complex network of interplay among the invading virus, target cells and host immune responses. Viruses use various strategies to evade or delay the cytokine response, gaining additional time to replicate in the host. In this review, we summarize the impacts of CCL19 and CCR7 expression on the regulation of viral pathogenesis with an emphasis on the corresponding signaling pathways and adjuvant mechanisms. We present and discuss the expression, signaling adaptor proteins and effects of CCL19 and CCR7 as these molecules differentially impact different viral infections and viral life cycles in host homeostatic strategies. The underlying mechanisms discussed in this review may assist in the design of novel agents to modulate chemokine activity for viral prevention.
机译:趋化因子(CC主题)配体19(CCL19)是在持续免疫监视,体内稳态和发育过程中诱导T细胞活化,免疫耐受和炎症反应的关键调节剂。 CC趋化因子受体7(CCR7)表达细胞向次级淋巴器官的迁移是适应性免疫发作的关键步骤,适应性免疫是由CCR7及其同源配体之间的复杂相互作用引发的。关于CCL19-CCR7轴对病毒感染的反应的最新知识进展阐明了入侵病毒,靶细胞和宿主免疫反应之间相互作用的复杂网络。病毒使用各种策略来逃避或延迟细胞因子的反应,从而在宿主中获得更多的复制时间。在这篇综述中,我们总结了CCL19和CCR7表达对病毒发病机制调控的影响,重点是相应的信号通路和佐剂机制。我们提出并讨论了表达,信号转导接头蛋白以及CCL19和CCR7的作用,因为这些分子在宿主体内稳态策略中差异地影响了不同的病毒感染和病毒生命周期。在这篇综述中讨论的潜在机制可能有助于设计新型药物来调节趋化因子的活性以预防病毒。

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