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From CAR-T Cells to CAR-NK Cells: A Developing Immunotherapy Method for Hematological Malignancies.

作者信息

Lu Hui, Zhao Xiaoyan, Li Ziying, Hu Yu, Wang Huafang

机构信息

Department of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Front Oncol. 2021 Aug 6;11:720501. doi: 10.3389/fonc.2021.720501. eCollection 2021.


DOI:10.3389/fonc.2021.720501
PMID:34422667
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8377427/
Abstract

The approval of CD19 chimeric antigen receptor (CAR)-engineered T (CAR-T) cell products in B-cell malignancies represents a breakthrough in CAR-T cell immunotherapy. However, the remaining limitations concerning the graft-versus-host disease (GVHD) and other adverse effects (e.g., cytokine release syndromes [CRS] and neurotoxicity) still restrict their wider applications. Natural killer (NK) cells have been identified as promising candidates for CAR-based cellular immunotherapy because of their unique characteristics. No HLA-matching restriction and abundant sources make CAR-engineered NK (CAR-NK) cells potentially available to be off-the-shelf products that could be readily available for immediate clinical use. Therefore, researchers have gradually shifted their focus from CAR-T cells to CAR-NK cells in hematological malignancies. This review discusses the current status and applications of CAR-NK cells in hematological malignancies, as well as the unique advantages of CAR-NK cells compared with CAR-T cells. It also discusses challenges and prospects regarding clinical applications of CAR-NK cells.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36b7/8377427/8399fccd7575/fonc-11-720501-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36b7/8377427/a1af4d50856f/fonc-11-720501-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36b7/8377427/8399fccd7575/fonc-11-720501-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36b7/8377427/a1af4d50856f/fonc-11-720501-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36b7/8377427/8399fccd7575/fonc-11-720501-g002.jpg

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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Natural Killer cells and monoclonal antibodies: Two partners for successful antibody dependent cytotoxicity against tumor cells.

Crit Rev Oncol Hematol. 2021-4

[2]
Anti-CD19 CAR-T cell therapy bridge to HSCT decreases the relapse rate and improves the long-term survival of R/R B-ALL patients: a systematic review and meta-analysis.

Ann Hematol. 2021-4

[3]
FDA approves fourth CAR-T cell therapy.

Nat Rev Drug Discov. 2021-3

[4]
Engineering NK Cells for CAR Therapy-Recent Advances in Gene Transfer Methodology.

Front Immunol. 2020

[5]
Outlook for New CAR-Based Therapies with a Focus on CAR NK Cells: What Lies Beyond CAR-Engineered T Cells in the Race against Cancer.

Cancer Discov. 2021-1

[6]
NK cells as adoptive cellular therapy for hematological malignancies: Advantages and hurdles.

Semin Hematol. 2020-10

[7]
Immunotherapy in Hematologic Malignancies: Emerging Therapies and Novel Approaches.

Int J Mol Sci. 2020-10-27

[8]
Targeting a cytokine checkpoint enhances the fitness of armored cord blood CAR-NK cells.

Blood. 2021-2-4

[9]
CAR-NK cells: A promising cellular immunotherapy for cancer.

EBioMedicine. 2020-9

[10]
Drug Resistance in Hematological Malignancies.

Int J Mol Sci. 2020-8-24

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