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自噬与Ⅰ型干扰素应答在固有抗病毒免疫中的相互作用。

Crosstalk between Autophagy and Type I Interferon Responses in Innate Antiviral Immunity.

机构信息

Department of Microbiology, Anhui Medical University, Hefei 230032, China.

Wuhu Interferon Bio-Products Industry Research Institute Co., Ltd., Wuhu 241000, China.

出版信息

Viruses. 2019 Feb 1;11(2):132. doi: 10.3390/v11020132.

Abstract

Autophagy exhibits dual effects during viral infections, promoting the clearance of viral components and activating the immune system to produce antiviral cytokines. However, some viruses impair immune defenses by collaborating with autophagy. Mounting evidence suggests that the interaction between autophagy and innate immunity is critical to understanding the contradictory roles of autophagy. Type I interferon (IFN-I) is a crucial antiviral factor, and studies have indicated that autophagy affects IFN-I responses by regulating IFN-I and its receptors expression. Similarly, IFN-I and interferon-stimulated gene (ISG) products can harness autophagy to regulate antiviral immunity. Crosstalk between autophagy and IFN-I responses could be a vital aspect of the molecular mechanisms involving autophagy in innate antiviral immunity. This review briefly summarizes the approaches by which autophagy regulates antiviral IFN-I responses and highlights the recent advances on the mechanisms by which IFN-I and ISG products employ autophagy against viruses.

摘要

自噬在病毒感染过程中表现出双重作用,既能促进病毒成分的清除,又能激活免疫系统产生抗病毒细胞因子。然而,一些病毒通过与自噬合作来破坏免疫防御。越来越多的证据表明,自噬与先天免疫之间的相互作用对于理解自噬的矛盾作用至关重要。I 型干扰素(IFN-I)是一种重要的抗病毒因子,研究表明自噬通过调节 IFN-I 及其受体的表达来影响 IFN-I 反应。同样,IFN-I 和干扰素刺激基因(ISG)产物可以利用自噬来调节抗病毒免疫。自噬与 IFN-I 反应之间的串扰可能是自噬参与先天抗病毒免疫的分子机制的一个重要方面。本文简要总结了自噬调节抗病毒 IFN-I 反应的途径,并强调了 IFN-I 和 ISG 产物利用自噬对抗病毒的机制的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322e/6409909/342068fb1f7c/viruses-11-00132-g001.jpg

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