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CAR 巨噬细胞:实体瘤及其他疾病有前景的新型免疫疗法

英文原题:CAR Macrophages: a promising novel immunotherapy for solid tumors and beyond.

查看英文原题

CAR Macrophages: a promising novel immunotherapy for solid tumors and beyond.

PubMed 2024/08/23(内容时间) Biomark Res Q1 · IF 14.6(JCR 2025)

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中文摘要

随着过继性细胞疗法的出现,嵌合抗原受体(CAR)-T 细胞疗法在癌症治疗中获得了广泛应用,并已对某些血液系统恶性肿瘤显示出显著疗效。然而,由于 CAR-T 细胞疗法在治疗实体瘤方面的局限性,其他免疫细胞正被用 CAR 进行改造以解决这一问题。巨噬细胞已成为一种有前景的选择,因其具有广泛的免疫功能,包括抗原呈递、强大的肿瘤吞噬作用,尤其是向肿瘤微环境的活跃迁移。借助其独特优势,CAR-巨噬细胞(CAR-M)有望作为一种新型免疫疗法增强实体瘤治疗的效果,并可能克服与 CAR-T/NK 疗法相关的主要挑战。本综述概述了 CAR-M 的主要机制以及 CAR-M 疗法的最新进展,同时也讨论了其进一步应用。

展开英文摘要原文

With the advent of adoptive cellular therapy, chimeric antigen receptor (CAR)-T cell therapy has gained widespread application in cancer treatment and has demonstrated significant efficacy against certain hematologic malignancies.

However, due to the limitations of CAR-T cell therapy in treating solid tumors, other immune cells are being modified with CAR to address this issue. Macrophages have emerged as a promising option, owing to their extensive immune functions, which include antigen presentation, powerful tumor phagocytosis, and particularly active trafficking to the tumor microenvironment.

Leveraging their unique advantages, CAR-macrophages (CAR-M) are expected to enhance the effectiveness of solid tumor treatments as a novel form of immunotherapy, potentially overcoming major challenges associated with CAR-T/NK therapy. This review outlines the primary mechanism underlying CAR-M and recent progressions in CAR-M therapy, while also discussing their further applications.

论文信息

作者
Lu J、Ma Y、Li Q、Xu Y、Xue Y、Xu S
第一作者单位
National Key Lab of Immunity and Inflammation and Institute of Immunology, Naval Medical University/Second Military Medical University, Shanghai, 200433, China.China
通讯作者单位
National Key Lab of Immunity and Inflammation and Institute of Immunology, Naval Medical University/Second Military Medical University, Shanghai, 200433, China. xusheng@immunol.org.China
文献类型
综述
期刊
Biomarker research2024 Aug 23
原文标识
PubMed 39175095 · DOI 10.1186/s40364-024-00637-2