Skip to content
DraconiticResearch
Search Sources API
220,595 studies31 sourcesUpdated 34 min ago
Peer-reviewedCC BY-NC-ND 4.0Journal of Translational Medicine

CAR-Macrophage therapy for digestive system tumors: mechanisms, engineering and translational prospects

  1. 1The Second Hospital of Lanzhou University (Second Clinical Medical College), No. 82, Cuiyingmen, Chengguan District, Lanzhou City, Gansu Province China
  2. 2Gansu Province Key Laboratory of Environmental Oncology, Lanzhou City, Gansu Province China
  3. 3Department of General Surgery, The Second Hospital of Lanzhou University (Second Clinical Medical College), Lanzhou University, Lanzhou City, Gansu Province China

Abstract

Chimeric antigen receptor T-cell (CAR-T) therapy has achieved remarkable outcomes in the treatment of hematological malignancies, yet its efficacy is severely compromised in digestive system tumors. The inherent physical barriers and immunosuppressive tumor microenvironment (TME) of digestive tumors hinder the infiltration and effector function of antitumor immune cells, greatly limiting the efficacy of conventional immunotherapies and creating an urgent demand for novel targeted immunotherapeutic strategies. As pivotal resident immune cells in the TME, macrophages possess powerful phagocytic activity and antigen-presenting ability, making them ideal candidates for tumor immunotherapy. Chimeric antigen receptor macrophages (CAR-Ms) can penetrate and remodel the immunosuppressive TME and directly eliminate tumor cells, exhibiting unique advantages and great application potential for the treatment of digestive system tumors. Herein, we provide a comprehensive narrative review of the latest research advances in CAR-M therapy for digestive system tumors. This review mainly focuses on the cellular origins, innovative engineering and genetic modification strategies, and underlying antitumor mechanisms of CAR-Ms, as well as systematically discusses the current challenges and future prospects of CAR-M-based digestive tumor therapy. We aim to provide valuable theoretical references for the development and clinical translation of novel immunotherapies for digestive system tumors. With the rapid development of precision immunomedicine, CAR-M therapy is expected to become a promising alternative therapeutic strategy for clinical digestive system tumors treatment.

Related

  1. Plant-derived extracellular vesicles in musculoskeletal disorders: a narrative review of mechanisms, therapeutic efficacy, and translational prospects
    Qixuan Jiang, Lei Chen, Junyan Li +7
    Frontiers in PharmacologyPeer-reviewedCC BY 4.0Pharmacology & toxicologyFrontiersCrossref
  2. Tanshinone IIA in colorectal cancer: preclinical mechanisms, therapeutic sensitization, and translational prospects
    Siqin Li, Jingzhi Zhang, Xiaoyu Zhang +6
    Frontiers in PharmacologyPeer-reviewedCC BY 4.0Pharmacology & toxicologyFrontiersCrossref
  3. Mechanisms and Clinical Translational Prospects of the Microbiota–Gut–Lung Axis in Connective Tissue Disease-Associated Interstitial Lung Disease
    Junxia Hu, Shiwen Ke, Lisha Mo +3
    BiomoleculesPeer-reviewedCC BY 4.0Full textGeneral medicineCrossrefEurope PMC
  4. Selenium Nanoparticles in Atherosclerosis and Non-Alcoholic Fatty Liver Disease: A Comprehensive Review of Therapeutic Mechanisms, Targeted Delivery, and Translational Prospects
    Keqian Chen, Shu-Zhi Wang
    International Journal of NanomedicinePeer-reviewedCC BY-NC 4.0Full textGeneral medicineDOAJPMC
  5. Engineering CAR-T cell therapies for digestive tract cancer: advances, challenges, and strategies to overcome tumor heterogeneity and immunosuppressive barriers.
    Qiaoyan Qu, Jintan Xiao, Bingjian Zhao +1
    Neoplasia (New York, N.Y.)Peer-reviewedCC BY-NC-NDFull textOncologyEurope PMC
BibTeX
@article{wu2026carmacrophage,
  title = {{CAR-Macrophage therapy for digestive system tumors: mechanisms, engineering and translational prospects}},
  author = {Wenzhang Wu and Daijun Wang and Yumin Li},
  journal = {Journal of Translational Medicine},
  year = {2026},
  month = jul,
  doi = {10.1186/s12967-026-08543-x},
  url = {https://doi.org/10.1186/s12967-026-08543-x},
  note = {CC BY-NC-ND 4.0},
}
RIS
TY  - JOUR
TI  - CAR-Macrophage therapy for digestive system tumors: mechanisms, engineering and translational prospects
AU  - Wenzhang Wu
AU  - Daijun Wang
AU  - Yumin Li
PY  - 2026
DA  - 2026/07/07
JO  - Journal of Translational Medicine
DO  - 10.1186/s12967-026-08543-x
UR  - https://doi.org/10.1186/s12967-026-08543-x
AB  - Chimeric antigen receptor T-cell (CAR-T) therapy has achieved remarkable outcomes in the treatment of hematological malignancies, yet its efficacy is severely compromised in digestive system tumors. The inherent physical barriers and immunosuppressive tumor microenvironment (TME) of digestive tumors hinder the infiltration and effector function of antitumor immune cells, greatly limiting the efficacy of conventional immunotherapies and creating an urgent demand for novel targeted immunotherapeutic strategies. As pivotal resident immune cells in the TME, macrophages possess powerful phagocytic activity and antigen-presenting ability, making them ideal candidates for tumor immunotherapy. Chimeric antigen receptor macrophages (CAR-Ms) can penetrate and remodel the immunosuppressive TME and directly eliminate tumor cells, exhibiting unique advantages and great application potential for the treatment of digestive system tumors. Herein, we provide a comprehensive narrative review of the latest research advances in CAR-M therapy for digestive system tumors. This review mainly focuses on the cellular origins, innovative engineering and genetic modification strategies, and underlying antitumor mechanisms of CAR-Ms, as well as systematically discusses the current challenges and future prospects of CAR-M-based digestive tumor therapy. We aim to provide valuable theoretical references for the development and clinical translation of novel immunotherapies for digestive system tumors. With the rapid development of precision immunomedicine, CAR-M therapy is expected to become a promising alternative therapeutic strategy for clinical digestive system tumors treatment.
SN  - 1479-5876
ER  -