Tumor-associated macrophages (TAMs): Constructing an immunosuppressive microenvironment bridge for pancreatic ductal adenocarcinoma (PDAC)

Runjie Liu , Jianang Li , Liang Liu , Wenquan Wang , Jinbin Jia
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Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a fatal disease with increasing incidences worldwide. The overall 5-year survival rate remains low, underscoring the urgent need for effective therapies. Despite the promising efficacy of immunotherapy for various solid tumors, its benefits for pancreatic cancer have been disappointing. This is largely because of the complex and unique mechanisms of immune evasion inherent in PDAC. Emerging evidence has highlighted the pivotal role of tumor-associated macrophages (TAMs) in facilitating the immune escape of PDAC. TAMs significantly contribute to forming an immunosuppressive microenvironment, which hinders the effectiveness of immunotherapeutic approaches. They achieve this through multiple pathways, including the secretion of cytokines and the promotion or inhibition of multiple immune cells. In this review, we summarized the main pathways through which TAMs form an immunosuppressive microenvironment in PDAC. We also examined the current status and recent progress of immunotherapy strategies that specifically target macrophages. By understanding these mechanisms and exploring targeted therapies, we aimed to shed light on potential avenues for improving the treatment outcomes of this devastating disease.

Abstract Image

肿瘤相关巨噬细胞(TAMs):为胰腺导管腺癌(PDAC)搭建免疫抑制微环境桥梁
胰腺导管腺癌(Pancreatic ductal adencarcinoma, PDAC)是一种世界范围内发病率不断上升的致命性疾病。总体5年生存率仍然很低,强调迫切需要有效的治疗。尽管免疫疗法对各种实体瘤有很好的疗效,但它对胰腺癌的疗效却令人失望。这主要是因为PDAC固有的复杂和独特的免疫逃避机制。新出现的证据强调了肿瘤相关巨噬细胞(tam)在促进PDAC免疫逃逸中的关键作用。tam明显有助于形成免疫抑制微环境,这阻碍了免疫治疗方法的有效性。它们通过多种途径实现这一目标,包括分泌细胞因子和促进或抑制多种免疫细胞。本文综述了tam在PDAC中形成免疫抑制微环境的主要途径。我们还研究了特异性靶向巨噬细胞的免疫治疗策略的现状和最新进展。通过了解这些机制和探索靶向治疗,我们旨在揭示改善这种毁灭性疾病治疗结果的潜在途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer pathogenesis and therapy
Cancer pathogenesis and therapy Surgery, Radiology and Imaging, Cancer Research, Oncology
CiteScore
0.80
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54 days
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