← 返回

基于巨噬细胞的肿瘤免疫治疗:挑战与机遇

英文原题:Macrophage-based cancer immunotherapy: Challenges and opportunities.

查看英文原题

Macrophage-based cancer immunotherapy: Challenges and opportunities.

PubMed 2024/08/03(内容时间) Exp Cell Res Q2 · IF 3.5(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

巨噬细胞在肿瘤微环境(TME)中发挥着关键作用,其功能多样,既包括促进肿瘤生长和转移,也包括协调抗肿瘤免疫应答。其可塑性使它们能够采取不同的激活状态,通常称为M1样(促炎性)和M2样(抗炎性或促肿瘤性),显著影响肿瘤进展和治疗反应。利用巨噬细胞在癌症免疫治疗中的潜力已成为一种有前景的策略,针对这些细胞直接靶向或调节其在TME内功能的兴趣日益增加。本综述探讨了巨噬细胞、TME与免疫治疗方法之间复杂的相互作用。我们讨论了肿瘤相关巨噬细胞(TAMs)的动态表型和功能异质性、它们对疾病进展的影响,以及它们对免疫治疗应答的机制。此外,我们重点介绍了基于巨噬细胞的免疫治疗策略的最新进展,包括巨噬细胞靶向药物、过继细胞转移和工程化方法。理解巨噬细胞与TME之间复杂的串扰对于开发有效的免疫治疗干预措施至关重要,这些措施利用巨噬细胞的免疫调节功能来增强抗肿瘤免疫并改善癌症患者的临床结局。

展开英文摘要原文

Macrophages play crucial roles in the tumor microenvironment (TME), exerting diverse functions ranging from promoting tumor growth and metastasis to orchestrating anti-tumor immune responses. Their plasticity allows them to adopt distinct activation states, often called M1-like (pro-inflammatory) and M2-like (anti-inflammatory or pro-tumoral), significantly influencing tumor progression and response to therapy.

Harnessing the potential of macrophages in cancer immunotherapy has emerged as a promising strategy, with increasing interest in targeting these cells directly or modulating their functions within the TME. This review explores the intricate interplay between macrophages, the TME, and immunotherapeutic approaches.

We discuss the dynamic phenotypic and functional heterogeneity of tumor-associated macrophages (TAMs), their impact on disease progression, and the mechanisms underlying their response to immunotherapy.

Furthermore, we highlight recent advancements in macrophage-based immunotherapeutic strategies, including macrophage-targeting agents, adoptive cell transfer, and engineering approaches. Understanding the complex crosstalk between macrophages and the TME is essential for developing effective immunotherapeutic interventions that exploit the immunomodulatory functions of macrophages to enhance anti-tumor immunity and improve clinical outcomes for cancer patients.

论文信息

作者
Bai H、Feng L、Schmid F
第一作者单位
Division of Natural and Applied Sciences, Duke Kunshan University, Kunshan, Jiangsu, 215316, China; Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 21205, USA. Electronic address: hbai23@jh.edu.China
通讯作者单位
School of Biomedical Sciences, Carleton University, Ottawa, Canada. Electronic address: rmgi363667@outlook.com.Canada
文献类型
综述
期刊
Experimental cell research2024 Sep 1
原文标识
PubMed 39103071 · DOI 10.1016/j.yexcr.2024.114198