Related Experiment Video
Updated: Jan 10, 2026

Studying Interactions between Myeloid Cells and CAR T Cells In Vitro and In Vivo
Published on: July 25, 2025
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.
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.
Insights
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.
Related Concept Videos
Tumor Progression
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Targeted Cancer Therapies
There are several types of targeted therapies against...
Tumor Immunotherapy
The Tumor Microenvironment

