CAR-macrophages in solid tumors: promise, progress, and prospects

Chimeric antigen receptor macrophages (CAR-Ms) represent a promising frontier in immunotherapy, leveraging both innate and engineered capabilities to combat solid tumors. CAR-Ms can actively remodel the tumor microenvironment while directly targeting tumor cells through CAR signaling, making them a potential alternative to existing cell-based therapies. Pre-clinical and clinical evidence suggests that CAR-M therapy holds significant promise for treating solid tumors. However, its clinical translation remains challenging due to restricted cell expansion, genetic engineering complexities, and variability in product quality. This article reviews recent advances in the CAR-M field, discussing the biological rationale behind this approach, key preclinical findings, and technological innovations necessary to facilitate clinical success as a versatile, off the shelf immunotherapy for hard-to-treat solid malignancies.

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Institutions

Publication Details

Journal
npj Precision Oncology
Published
2025-11-27
DOI
https://doi.org/10.1038/s41698-025-01170-7
Citations
11
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
11.50

Funders

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article

CAR-macrophages in solid tumors: promise, progress, and prospects

Qasim A. Rafiq, Rana Khalife, Pedro Silva Couto, Maram Alrehaili
11 citations
npj Precision Oncology
CAR-T cell therapy research
11.50
article

CAR-macrophages in solid tumors: promise, progress, and prospects

Qasim A. Rafiq, Rana Khalife, Pedro Silva Couto, Maram Alrehaili
article en
11 citations

Abstract

Chimeric antigen receptor macrophages (CAR-Ms) represent a promising frontier in immunotherapy, leveraging both innate and engineered capabilities to combat solid tumors. CAR-Ms can actively remodel the tumor microenvironment while directly targeting tumor cells through CAR signaling, making them a potential alternative to existing cell-based therapies. Pre-clinical and clinical evidence suggests that CAR-M therapy holds significant promise for treating solid tumors. However, its clinical translation remains challenging due to restricted cell expansion, genetic engineering complexities, and variability in product quality. This article reviews recent advances in the CAR-M field, discussing the biological rationale behind this approach, key preclinical findings, and technological innovations necessary to facilitate clinical success as a versatile, off the shelf immunotherapy for hard-to-treat solid malignancies.

npj Precision OncologyVol. 9(1)
Biochemical Society (GB), University College London (GB)
UK Research and Innovation, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 1%
CAR-T cell therapy research
11.50
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