Litcius/Paper detail

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

Maram Alrehaili, Pedro Silva Couto, Rana Khalife, Qasim A. Rafiq

2025npj Precision Oncology20 citationsDOIOpen Access PDF

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.

Topics & Concepts

Chimeric antigen receptorImmunotherapyTranslation (biology)Computational biologyComputer scienceRisk analysis (engineering)NanotechnologyKey (lock)MedicineTumor microenvironmentProduct (mathematics)Biochemical engineeringSolid tumorOff the shelfInnate immune systemCell therapyImmunologyComponent (thermodynamics)BiologyClinical PracticeEngineering ethicsFrontierEngineeringTumor cellsCancer researchCAR-T cell therapy researchImmune cells in cancerPhagocytosis and Immune Regulation