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Chimeric antigen receptor-natural killer cells: a promising sword against insidious tumor cells.

作者信息

Hojjatipour Tahereh, Sharifzadeh Zahra, Maali Amirhosein, Azad Mehdi

机构信息

Department of Hematology and Blood Transfusion, Students Research Center, School of Allied Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Department of Immunology, Pasteur Institute of Iran, Tehran, Iran.

出版信息

Hum Cell. 2023 Nov;36(6):1843-1864. doi: 10.1007/s13577-023-00948-w. Epub 2023 Jul 21.


DOI:10.1007/s13577-023-00948-w
PMID:37477869
Abstract

Natural killer (NK) cells are a critical component of innate immunity, particularly in initial cancer recognition and inhibition of additional tumor growth or metastasis propagation. NK cells recognize transformed cells without prior sensitization via stimulatory receptors and rapidly eradicate them. However, the protective tumor microenvironment facilitates tumor escaping via induction of an exhaustion state in immune cells, including NK cells. Hence, genetic manipulation of NK cells for specific identification of tumor-associated antigens or a more robust response against tumor cells is a promising strategy for NK cells' tumoricidal augmentation. Regarding the remarkable achievement of engineered CAR-T cells in treating hematologic malignancies, there is evolving interest in CAR-NK cell recruitment in cancer immunotherapy. Innate functionality of NK cells, higher safety, superior in vivo maintenance, and the off-the-shelf potential move CAR-NK-based therapy superior to CAR-T cells treatment. In this review, we have comprehensively discussed the recent genetic manipulations of CAR-NK cell manufacturing regarding different domains of CAR constructs and their following delivery systems into diverse sources of NK cells. Then highlight the preclinical and clinical investigations of CAR-NK cells and examine the current challenges and prospects as an optimistic remedy in cancer immunotherapy.

摘要

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[2]
sBCMA Plasma Level Dynamics and Anti-BCMA CAR-T-Cell Treatment in Relapsed Multiple Myeloma.

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[3]
Directing CAR NK Cells via the Metabolic Incorporation of CAR Ligands into Malignant Cell Glycans.

ACS Chem Biol. 2022-6-17

[4]
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[5]
CD34 progenitor-derived NK cell and gemcitabine combination therapy increases killing of ovarian cancer cells in NOD/SCID/IL2Rg mice.

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[6]
Chimeric Antigen Receptor-T Cells: A Pharmaceutical Scope.

Front Pharmacol. 2021-8-20

[7]
Bactericidal fully human single-chain fragment variable antibodies protect mice against methicillin-resistant bacteraemia.

Clin Transl Immunology. 2021-6-29

[8]
Induced pluripotent stem cell technology: trends in molecular biology, from genetics to epigenetics.

Epigenomics. 2021-4

[9]
Transcription Factors Associated With IL-15 Cytokine Signaling During NK Cell Development.

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[10]
Current status and perspective of CAR-T and CAR-NK cell therapy trials in Germany.

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