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免疫检查点阻断剂耐药机制概述

A Highlight of the Mechanisms of Immune Checkpoint Blocker Resistance.

作者信息

Huang Qian, Lei Yanna, Li Xiaoying, Guo Fukun, Liu Ming

机构信息

Laboratory of Signal Transduction and Molecular Targeted Therapy, Department of Medical Oncology, West China Hospital, Sichuan University, Chengdu, China.

Division of Experimental Hematology and Cancer Biology, Children's Hospital Medical Center, Cincinnati, OH, United States.

出版信息

Front Cell Dev Biol. 2020 Dec 4;8:580140. doi: 10.3389/fcell.2020.580140. eCollection 2020.

DOI:10.3389/fcell.2020.580140
PMID:33344447
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7746821/
Abstract

In recent years, as our understanding of tumor immunology is continuously improved, immunotherapy has come to the center stage of cancer therapy and is deemed as the most promising approach for cancer control. Although immunotherapy, particularly immune checkpoint blockade (ICB), has achieved a milestone in several types of tumors, the majority of cancer patients do not benefit from immunotherapy. The dismal outcome of cancer immunotherapy is mainly due to primary or acquired resistance arising from tumor immune evasion. Exploring the mechanisms of tumor immune evasion in the course of immunotherapy may identify biological targets to conquer tumor resistance to immunotherapy. In this review, we highlight tumor cell-intrinsic and -extrinsic factors that may underlie tumor resistance to immune checkpoint blockers. Targeting these factors in combination with immune checkpoint blockers points to the future direction of cancer immunotherapy.

摘要

近年来,随着我们对肿瘤免疫学的认识不断提高,免疫疗法已成为癌症治疗的核心,并被视为控制癌症最有前景的方法。尽管免疫疗法,尤其是免疫检查点阻断(ICB)在几种类型的肿瘤治疗中取得了里程碑式的进展,但大多数癌症患者并未从免疫疗法中获益。癌症免疫疗法令人沮丧的结果主要是由于肿瘤免疫逃逸产生的原发性或获得性耐药。在免疫治疗过程中探索肿瘤免疫逃逸的机制可能会识别出克服肿瘤对免疫治疗耐药性的生物学靶点。在这篇综述中,我们重点介绍了可能导致肿瘤对免疫检查点阻滞剂耐药的肿瘤细胞内在和外在因素。将这些因素与免疫检查点阻滞剂联合靶向治疗指明了癌症免疫治疗的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8f8/7746821/437b936f5640/fcell-08-580140-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8f8/7746821/437b936f5640/fcell-08-580140-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8f8/7746821/437b936f5640/fcell-08-580140-g001.jpg

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本文引用的文献

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ADORA1 Inhibition Promotes Tumor Immune Evasion by Regulating the ATF3-PD-L1 Axis.ADORA1 抑制通过调节 ATF3-PD-L1 轴促进肿瘤免疫逃逸。
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Recent insight into the role of FBXW7 as a tumor suppressor.近期对 FBXW7 作为肿瘤抑制因子的作用的深入了解。
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The role of macrophages in the tumor microenvironment and tumor metabolism.巨噬细胞在肿瘤微环境和肿瘤代谢中的作用。
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Harnessing the Immune System with Cancer Vaccines: From Prevention to Therapeutics.利用癌症疫苗激发免疫系统:从预防到治疗
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Mechanisms of Immunotherapy Resistance in Cutaneous Melanoma: Recognizing a Shapeshifter.皮肤黑色素瘤免疫治疗耐药机制:认识一个善变者。
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Disrupting cancer angiogenesis and immune checkpoint networks for improved tumor immunity.破坏癌症血管生成和免疫检查点网络以增强肿瘤免疫。
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Tumor promoting roles of IL-10, TGF-β, IL-4, and IL-35: Its implications in cancer immunotherapy.白细胞介素-10、转化生长因子-β、白细胞介素-4和白细胞介素-35的肿瘤促进作用:其在癌症免疫治疗中的意义。
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