Facts and Hopes of Chimeric Antigen Receptor–Redirected NK T Cells

Chimeric antigen receptor (CAR)-engineered invariant NK T cells (CAR-NKT) are a novel cell platform for cancer immunotherapy. Unlike conventional T cells, NKTs are characterized by innate antitumor properties, minimal alloreactivity, and a unique ability to modulate the tumor microenvironment. This article provides a comprehensive overview of preclinical and early clinical studies evaluating CAR-NKTs in both autologous and allogeneic clinical settings. We discuss the contributions of CAR signaling domains, cytokine coexpression, and other functional measures that correlate with CAR-NKT persistence, function, and metabolic fitness. We also discuss the critical role of immunocompetent animal models in elucidating the interactions of CAR-NKTs with the tumor microenvironment and other components of the immune system. Finally, we review strategies that combine CAR-NKTs with other therapeutic approaches to promote potential synergistic benefits in patients with cancer.

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Publication Details

Journal
Clinical Cancer Research
Published
2025-10-21
DOI
https://doi.org/10.1158/1078-0432.ccr-25-0197
Citations
1
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
0.80
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article

Facts and Hopes of Chimeric Antigen Receptor–Redirected NK T Cells

Amy N. Courtney, Gianpietro Dotti, Ying Wang, Gengwen Tian et al.
1 citations
Clinical Cancer Research
Immune Cell Function and Interaction
0.80
article

Facts and Hopes of Chimeric Antigen Receptor–Redirected NK T Cells

Amy N. Courtney, Gianpietro Dotti, Ying Wang, Gengwen Tian, Leonid S. Metelitsa, Xin Zhou
article en
1 citations

Abstract

Chimeric antigen receptor (CAR)-engineered invariant NK T cells (CAR-NKT) are a novel cell platform for cancer immunotherapy. Unlike conventional T cells, NKTs are characterized by innate antitumor properties, minimal alloreactivity, and a unique ability to modulate the tumor microenvironment. This article provides a comprehensive overview of preclinical and early clinical studies evaluating CAR-NKTs in both autologous and allogeneic clinical settings. We discuss the contributions of CAR signaling domains, cytokine coexpression, and other functional measures that correlate with CAR-NKT persistence, function, and metabolic fitness. We also discuss the critical role of immunocompetent animal models in elucidating the interactions of CAR-NKTs with the tumor microenvironment and other components of the immune system. Finally, we review strategies that combine CAR-NKTs with other therapeutic approaches to promote potential synergistic benefits in patients with cancer.

Clinical Cancer ResearchVol. 31(24)
University of North Carolina at Chapel Hill (US), Baylor College of Medicine (US), China Academy of Chinese Medical Sciences (CN), Children's Cancer Center (US), UNC Lineberger Comprehensive Cancer Center
Openalex Percentile: Top 22%
Immune Cell Function and Interaction
0.80
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