» Articles » PMID: 32853984

CAR-NK Cells: A Promising Cellular Immunotherapy for Cancer

Overview
Journal EBioMedicine
Date 2020 Aug 28
PMID 32853984
Citations 355
Authors
Affiliations
Soon will be listed here.
Abstract

Natural Killer (NK) cells and CD8 cytotoxic T cells are two types of immune cells that can kill target cells through similar cytotoxic mechanisms. With the remarkable success of chimeric antigen receptor (CAR)-engineered T (CAR-T) cells for treating haematological malignancies, there is a rapid growing interest in developing CAR-engineered NK (CAR-NK) cells for cancer therapy. Compared to CAR-T cells, CAR-NK cells could offer some significant advantages, including: (1) better safety, such as a lack or minimal cytokine release syndrome and neurotoxicity in autologous setting and graft-versus-host disease in allogenic setting, (2) multiple mechanisms for activating cytotoxic activity, and (3) high feasibility for 'off-the-shelf' manufacturing. CAR-NK cells could be engineered to target diverse antigens, enhance proliferation and persistence in vivo, increase infiltration into solid tumours, overcome resistant tumour microenvironment, and ultimately achieve an effective anti-tumour response. In this review, we focus on recent progress in genetic engineering and clinical application of CAR-NK cells, and discuss current challenges and future promise of CAR-NK cells as a novel cellular immunotherapy in cancer.

Citing Articles

Current Landscape and Future Directions in Cancer Immunotherapy: Therapies, Trials, and Challenges.

Bandara S, Raveendran S Cancers (Basel). 2025; 17(5).

PMID: 40075668 PMC: 11899461. DOI: 10.3390/cancers17050821.


Targeting HER2-Positive Solid Tumors with CAR NK Cells: CD44 Expression Is a Critical Modulator of HER2-Specific CAR NK Cell Efficacy.

Gergely B, Vereb M, Rebenku I, Vereb G, Szoor A Cancers (Basel). 2025; 17(5).

PMID: 40075578 PMC: 11898473. DOI: 10.3390/cancers17050731.


Bone marrow immune cells and drug resistance in acute myeloid leukemia.

Zhang M, Yang Y, Liu J, Guo L, Guo Q, Liu W Exp Biol Med (Maywood). 2025; 250:10235.

PMID: 40008144 PMC: 11851207. DOI: 10.3389/ebm.2025.10235.


Identification of CKAP2 as a Potential Target for Prevention of Gastric Cancer Progression: A Multi-Omics Study.

Liu X, Zhang W, Wang H, Yang W Int J Mol Sci. 2025; 26(4).

PMID: 40004022 PMC: 11855583. DOI: 10.3390/ijms26041557.


Advancing Immunotherapy in Pancreatic Cancer: A Brief Review of Emerging Adoptive Cell Therapies.

Sherpally D, Manne A Cancers (Basel). 2025; 17(4).

PMID: 40002184 PMC: 11853216. DOI: 10.3390/cancers17040589.


References
1.
Hunter B, Jacobson C . CAR T-Cell Associated Neurotoxicity: Mechanisms, Clinicopathologic Correlates, and Future Directions. J Natl Cancer Inst. 2019; 111(7):646-654. DOI: 10.1093/jnci/djz017. View

2.
Floch V, Audrezet M, Guillaume C, Gobin E, Le Bolch G, Clement J . Transgene expression kinetics after transfection with cationic phosphonolipids in hematopoietic non adherent cells. Biochim Biophys Acta. 1998; 1371(1):53-70. DOI: 10.1016/s0005-2736(98)00002-9. View

3.
Guven H, Konstantinidis K, Alici E, Aints A, Abedi-Valugerdi M, Christensson B . Efficient gene transfer into primary human natural killer cells by retroviral transduction. Exp Hematol. 2005; 33(11):1320-8. DOI: 10.1016/j.exphem.2005.07.006. View

4.
Li Y, Hermanson D, Moriarity B, Kaufman D . Human iPSC-Derived Natural Killer Cells Engineered with Chimeric Antigen Receptors Enhance Anti-tumor Activity. Cell Stem Cell. 2018; 23(2):181-192.e5. PMC: 6084450. DOI: 10.1016/j.stem.2018.06.002. View

5.
Lanier L . Up on the tightrope: natural killer cell activation and inhibition. Nat Immunol. 2008; 9(5):495-502. PMC: 2669298. DOI: 10.1038/ni1581. View