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I 型干扰素在抗肿瘤免疫中的双重作用。

A Dual Role of Type I Interferons in Antitumor Immunity.

机构信息

Jiangsu Key Laboratory of Infection and Immunity, The Institutes of Biology and Medical Sciences, Soochow University, Suzhou, 215123, P. R. China.

Department of Surgery, School of Medicine, UC Davis, Davis, CA, 95817, USA.

出版信息

Adv Biosyst. 2020 Nov;4(11):e1900237. doi: 10.1002/adbi.201900237. Epub 2020 Mar 13.

Abstract

Type I interferons (IFN-Is) are a family of cytokines that exert direct antiviral effects and regulate innate and adaptive immune responses through direct and indirect mechanisms. It is generally believed that IFN-Is repress tumor development via restricting tumor proliferation and inducing antitumor immune responses. However, recent emerging evidence suggests that IFN-Is play a dual role in antitumor immunity. That is, in the early stage of tumorigenesis, IFN-Is promote the antitumor immune response by enhancing antigen presentation in antigen-presenting cells and activating CD8 T cells. However, in the late stage of tumor progression, persistent expression of IFN-Is induces the expression of immunosuppressive factors (PD-L1, IDO, and IL-10) on the surface of dendritic cells and other bone marrow cells and inhibits their antitumor immunity. This review outlines these dual functions of IFN-Is in antitumor immunity and elucidates the involved mechanisms, as well as their applications in tumor therapy.

摘要

I 型干扰素(IFN-Is)是一类细胞因子,通过直接和间接机制发挥直接抗病毒作用,并调节先天和适应性免疫反应。人们普遍认为,IFN-Is 通过限制肿瘤增殖和诱导抗肿瘤免疫反应来抑制肿瘤的发展。然而,最近的新证据表明,IFN-Is 在抗肿瘤免疫中发挥双重作用。也就是说,在肿瘤发生的早期,IFN-Is 通过增强抗原呈递细胞中的抗原呈递和激活 CD8 T 细胞来促进抗肿瘤免疫反应。然而,在肿瘤进展的晚期,IFN-Is 的持续表达诱导树突状细胞和其他骨髓细胞表面免疫抑制因子(PD-L1、IDO 和 IL-10)的表达,并抑制其抗肿瘤免疫。本综述概述了 IFN-Is 在抗肿瘤免疫中的这双重作用,并阐明了相关机制及其在肿瘤治疗中的应用。

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