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Updated: Jan 10, 2026

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Studying Interactions between Myeloid Cells and CAR T Cells In Vitro and In Vivo
Published on: July 25, 2025
733
CAR-macrophages in solid tumors: promise, progress, and prospects
Maram Alrehaili1, Pedro Silva Couto1, Rana Khalife1
1Department of Biochemical Engineering, Advanced Centre for Biochemical Engineering, University College London, London, UK.
NPJ Precision Oncology
|November 27, 2025
Summary
Chimeric antigen receptor macrophages (CAR-Ms) show promise for solid tumor immunotherapy by remodeling the tumor microenvironment. Overcoming challenges in cell expansion and engineering is key to their clinical success as an off-the-shelf therapy.
Area of Science:
- Immunotherapy
- Oncology
- Cellular Therapy
Background:
- Chimeric antigen receptor macrophages (CAR-Ms) are an emerging immunotherapy approach for solid tumors.
- CAR-Ms combine innate immune functions with engineered CAR signaling for direct tumor targeting and microenvironment modulation.
- Existing cell-based therapies face limitations, highlighting the need for novel strategies like CAR-Ms.
Purpose of the Study:
- To review recent advancements in CAR-M therapy for solid tumors.
- To discuss the biological rationale and preclinical findings supporting CAR-M efficacy.
- To identify technological innovations required for successful clinical translation of CAR-Ms.
Main Methods:
- Review of preclinical and clinical evidence on CAR-M therapy.
- Analysis of biological mechanisms of CAR-Ms in solid tumors.
- Discussion of technological challenges and innovations in CAR-M development.
Main Results:
- Preclinical and clinical data indicate significant promise for CAR-M therapy in solid tumors.
- CAR-Ms demonstrate potential to actively remodel the tumor microenvironment.
- CAR-Ms offer direct tumor cell targeting via CAR signaling.
Conclusions:
- CAR-M therapy is a promising immunotherapy strategy for solid tumors.
- Clinical translation is hindered by challenges in cell expansion, genetic engineering, and product quality.
- Technological innovations are crucial for developing CAR-Ms as a versatile, off-the-shelf immunotherapy for difficult-to-treat solid malignancies.
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