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嵌合抗原受体巨噬细胞:一种用于实体瘤及其他疾病的有前景的新型免疫疗法。

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

作者信息

Lu Jialin, Ma Yuqing, Li Qiuxin, Xu Yihuan, Xue Yiquan, Xu Sheng

机构信息

National Key Lab of Immunity and Inflammation and Institute of Immunology, Naval Medical University/Second Military Medical University, Shanghai, 200433, China.

Department of Gastroenterology, Changhai Hospital, Naval Medical University, Shanghai, 200433, China.

出版信息

Biomark Res. 2024 Aug 23;12(1):86. doi: 10.1186/s40364-024-00637-2.


DOI:10.1186/s40364-024-00637-2
PMID:39175095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11342599/
Abstract

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.

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得到了广泛应用,并已证明对某些血液系统恶性肿瘤具有显著疗效。然而,由于CAR-T细胞疗法在治疗实体瘤方面存在局限性,其他免疫细胞正被用CAR进行改造以解决这一问题。巨噬细胞因其广泛的免疫功能而成为一个有前景的选择,这些功能包括抗原呈递、强大的肿瘤吞噬作用,以及特别活跃地向肿瘤微环境迁移。利用其独特优势,CAR巨噬细胞(CAR-M)有望作为一种新型免疫疗法提高实体瘤治疗的有效性,有可能克服与CAR-T/NK疗法相关的主要挑战。本综述概述了CAR-M的主要作用机制以及CAR-M疗法的最新进展,同时也讨论了它们的进一步应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d227/11342599/7afa43f23799/40364_2024_637_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d227/11342599/f64808907c72/40364_2024_637_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d227/11342599/f9837e1a8871/40364_2024_637_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d227/11342599/e12e308b193a/40364_2024_637_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d227/11342599/7afa43f23799/40364_2024_637_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d227/11342599/f64808907c72/40364_2024_637_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d227/11342599/f9837e1a8871/40364_2024_637_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d227/11342599/e12e308b193a/40364_2024_637_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d227/11342599/7afa43f23799/40364_2024_637_Fig4_HTML.jpg

相似文献

[1]
CAR Macrophages: a promising novel immunotherapy for solid tumors and beyond.

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[2]
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[4]
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[5]
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[10]
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引用本文的文献

[1]
CAR-exosomes derived from immune cells: an emerging nanoscale vanguard in overcoming tumor immunotherapy hurdles.

Front Immunol. 2025-8-19

[2]
Emerging CAR immunotherapies: broadening therapeutic horizons beyond cancer.

Clin Exp Med. 2025-8-4

[3]
Engineering Innate Immunity: Recent Advances and Future Directions for CAR-NK and CAR-Macrophage Therapies in Solid Tumors.

Cancers (Basel). 2025-7-19

[4]
Recent advances and challenges of cellular immunotherapies in lung cancer treatment.

Exp Hematol Oncol. 2025-7-7

[5]
Advancing CAR-based cell therapies for solid tumours: challenges, therapeutic strategies, and perspectives.

Mol Cancer. 2025-7-7

[6]
Current challenges and emerging opportunities of chimeric antigen receptor-engineered cell immunotherapy.

Exp Hematol Oncol. 2025-7-2

[7]
Engineered immune cell therapies for solid tumors: pharmacological advances, clinical outcomes, and future directions.

Front Pharmacol. 2025-6-12

[8]
Unleashing the power of CAR-M therapy in solid tumors: a comprehensive review.

Front Immunol. 2025-6-12

[9]
Cell-Based Therapies for Solid Tumors: Challenges and Advances.

Int J Mol Sci. 2025-6-9

[10]
Advancing Breast Cancer Treatment: The Role of Immunotherapy and Cancer Vaccines in Overcoming Therapeutic Challenges.

Vaccines (Basel). 2025-3-24

本文引用的文献

[1]
Activating innate immune responses repolarizes hPSC-derived CAR macrophages to improve anti-tumor activity.

Cell Stem Cell. 2024-7-5

[2]
Human anti-PSCA CAR macrophages possess potent antitumor activity against pancreatic cancer.

Cell Stem Cell. 2024-6-6

[3]
Enhancing CAR Macrophage Efferocytosis Via Surface Engineered Lipid Nanoparticles Targeting LXR Signaling.

Adv Mater. 2024-5

[4]
Chimeric antigen receptor-modified macrophages ameliorate liver fibrosis in preclinical models.

J Hepatol. 2024-6

[5]
mRNA-Laden Lipid-Nanoparticle-Enabled CAR-Macrophage Engineering for the Eradication of Multidrug-Resistant Bacteria in a Sepsis Mouse Model.

ACS Nano. 2024-1-23

[6]
Generation of chimeric antigen receptor macrophages from human pluripotent stem cells to target glioblastoma.

Immunooncol Technol. 2023-10-4

[7]
Neutrophil activation and clonal CAR-T re-expansion underpinning cytokine release syndrome during ciltacabtagene autoleucel therapy in multiple myeloma.

Nat Commun. 2024-1-8

[8]
Scalable generation of functional human iPSC-derived CAR-macrophages that efficiently eradicate CD19-positive leukemia.

J Immunother Cancer. 2023-12-22

[9]
A second-generation M1-polarized CAR macrophage with antitumor efficacy.

Nat Immunol. 2024-1

[10]
The application of HER2 and CD47 CAR-macrophage in ovarian cancer.

J Transl Med. 2023-9-22

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