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肿瘤相关巨噬细胞调节 PD-1/PD-L1 免疫抑制。

Tumor-Associated Macrophages Regulate PD-1/PD-L1 Immunosuppression.

机构信息

Department of Medical Oncology and Cancer Institute, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

Front Immunol. 2022 May 3;13:874589. doi: 10.3389/fimmu.2022.874589. eCollection 2022.

Abstract

Anti-programmed cell death 1 (PD-1) or anti-PD-ligand (L) 1 drugs, as classic immune checkpoint inhibitors, are considered promising treatment strategies for tumors. In clinical practice, some cancer patients experience drug resistance and disease progression in the process of anti-PD-1/PD-L1 immunotherapy. Tumor-associated macrophages (TAMs) play key roles in regulating PD-1/PD-L1 immunosuppression by inhibiting the recruitment and function of T cells through cytokines, superficial immune checkpoint ligands, and exosomes. There are several therapies available to recover the anticancer efficacy of PD-1/PD-L1 inhibitors by targeting TAMs, including the inhibition of TAM differentiation and re-education of TAM activation. In this review, we will summarize the roles and mechanisms of TAMs in PD-1/PD-L1 blocker resistance. Furthermore, we will discuss the therapies that were designed to deplete TAMs, re-educate TAMs, and intervene with chemokines secreted by TAMs and exosomes from M1 macrophages, providing more potential options to improve the efficacy of PD-1/PD-L1 inhibitors.

摘要

抗程序性细胞死亡 1(PD-1)或抗 PD-配体 1(PD-L1)药物作为经典免疫检查点抑制剂,被认为是肿瘤治疗的有前途的策略。在临床实践中,一些癌症患者在接受抗 PD-1/PD-L1 免疫治疗的过程中会出现耐药和疾病进展。肿瘤相关巨噬细胞(TAMs)通过细胞因子、表面免疫检查点配体和外泌体抑制 T 细胞的募集和功能,在调节 PD-1/PD-L1 免疫抑制方面发挥关键作用。有几种方法可用于通过靶向 TAMs 来恢复 PD-1/PD-L1 抑制剂的抗癌疗效,包括抑制 TAM 分化和重新教育 TAM 激活。在这篇综述中,我们将总结 TAMs 在 PD-1/PD-L1 阻滞剂耐药中的作用和机制。此外,我们将讨论旨在消耗 TAMs、重新教育 TAMs 以及干预 TAMs 分泌的趋化因子和 M1 巨噬细胞来源的外泌体的疗法,为提高 PD-1/PD-L1 抑制剂的疗效提供更多潜在选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22f5/9110638/55967581fa7f/fimmu-13-874589-g001.jpg

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