Natural killer cells, macrophages and dendritic cells as innate immune therapies for blood cancers

Innate immune cells are emerging as powerful allies in the fight against blood cancers. Natural Killer (NK) cells, macrophages, and dendritic cells (DCs)—once viewed mainly as supporting players—are now at the forefront of next-generation immunotherapies, owing to their rapid, antigen-independent tumor recognition and potent effector functions. This review highlights their distinct anti-tumor roles: NK cells’ cytotoxicity and “missing-self” recognition, the dual and adaptable nature of macrophages in the tumor microenvironment (TME), and the antigen-presenting capabilities of DCs that bridge innate and adaptive immunity. We further examine transformative therapeutic strategies, including adoptive NK cell transfer, CAR-engineered NK cells (CAR-NK), CAR-macrophages (CAR-M), and DC vaccines, with a focus on clinical outcomes and safety—particularly the encouraging toxicity profile of CAR-NK cells. Despite these advances, major challenges persist, including limited persistence and homing of infused cells, TME-driven immunosuppression, and potential on-target/off-tumor effects. To overcome these barriers, synergistic approaches that integrate innate immune therapies with checkpoint inhibitors, conventional treatments, innovative engineering, and precise modulation of the TME will be essential. These strategies hold the promise of translating scientific breakthroughs into durable, safe, and widely accessible treatments for patients with hematological malignancies.

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Publication Details

Journal
Annals of Hematology
Published
2026-03-02
DOI
https://doi.org/10.1007/s00277-026-06872-x
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
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Natural killer cells, macrophages and dendritic cells as innate immune therapies for blood cancers

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Natural killer cells, macrophages and dendritic cells as innate immune therapies for blood cancers

Gunjan Mukherjee, Ashish Singh Chauhan, R Roopashree, Saodat Musayeva, Jayshree Nellore, Sajida Hussein Ismael, Ghaleb Oriquat, Waleed K. Abdulsahib
article en

Abstract

Innate immune cells are emerging as powerful allies in the fight against blood cancers. Natural Killer (NK) cells, macrophages, and dendritic cells (DCs)—once viewed mainly as supporting players—are now at the forefront of next-generation immunotherapies, owing to their rapid, antigen-independent tumor recognition and potent effector functions. This review highlights their distinct anti-tumor roles: NK cells’ cytotoxicity and “missing-self” recognition, the dual and adaptable nature of macrophages in the tumor microenvironment (TME), and the antigen-presenting capabilities of DCs that bridge innate and adaptive immunity. We further examine transformative therapeutic strategies, including adoptive NK cell transfer, CAR-engineered NK cells (CAR-NK), CAR-macrophages (CAR-M), and DC vaccines, with a focus on clinical outcomes and safety—particularly the encouraging toxicity profile of CAR-NK cells. Despite these advances, major challenges persist, including limited persistence and homing of infused cells, TME-driven immunosuppression, and potential on-target/off-tumor effects. To overcome these barriers, synergistic approaches that integrate innate immune therapies with checkpoint inhibitors, conventional treatments, innovative engineering, and precise modulation of the TME will be essential. These strategies hold the promise of translating scientific breakthroughs into durable, safe, and widely accessible treatments for patients with hematological malignancies.

Annals of HematologyVol. 105(4)
Chandigarh University (IN), Al-Ahliyya Amman University (JO), Jain University (IN), Siksha O Anusandhan University (IN), Al-Turath University (IQ), Alsalam University College (IQ), Uttaranchal University (IN), Institute of Medical Sciences and Sum Hospital (IN), Termez State University (UZ), Sathyabama Institute of Science and Technology (IN)
Openalex Percentile: Top 37%
Immune Cell Function and Interaction
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