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嵌合抗原受体(CAR)T细胞:B细胞恶性肿瘤中靶向CD19的经验教训。

Chimeric Antigen Receptor (CAR) T Cells: Lessons Learned from Targeting of CD19 in B-Cell Malignancies.

作者信息

Hay Kevin A, Turtle Cameron J

机构信息

Department of Medicine, University of British Columbia, Vancouver, BC, Canada.

Clinical Research Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave., Seattle, WA, 98109, USA.

出版信息

Drugs. 2017 Mar;77(3):237-245. doi: 10.1007/s40265-017-0690-8.


DOI:10.1007/s40265-017-0690-8
PMID:28110394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5603178/
Abstract

Adoptive immunotherapy with chimeric antigen receptor-modified (CAR)-T cells is a rapidly growing therapeutic approach to treating patients with refractory cancer, with over 100 clinical trials in various malignancies in progress. The enthusiasm for CAR-T cells has been driven by the clinical success of CD19-targeted CAR-T cell therapy in B-cell acute lymphoblastic leukemia, and the promising data in B-cell non-Hodgkin's lymphoma and chronic lymphocytic leukemia. Despite the success of targeting CD19 with CAR-T cells in early clinical studies, many challenges remain to improve outcomes, reduce toxicity, and determine the appropriate settings for CAR-T cell immunotherapy. Reviewing the lessons learned thus far in CD19 CAR-T cell trials and how some of these challenges may be overcome will help guide the development of CAR-T cell therapy for malignancies of B-cell origin, as well as for other hematopoietic and non-hematopoietic cancers.

摘要

嵌合抗原受体修饰(CAR)-T细胞过继性免疫疗法是一种发展迅速的治疗难治性癌症患者的方法,目前有100多项针对各种恶性肿瘤的临床试验正在进行。靶向CD19的CAR-T细胞疗法在B细胞急性淋巴细胞白血病中的临床成功,以及在B细胞非霍奇金淋巴瘤和慢性淋巴细胞白血病中获得的有前景的数据,推动了人们对CAR-T细胞的热情。尽管在早期临床研究中,CAR-T细胞靶向CD19取得了成功,但仍有许多挑战需要应对,以改善治疗效果、降低毒性,并确定CAR-T细胞免疫疗法的合适应用场景。回顾迄今为止在CD19 CAR-T细胞试验中吸取的经验教训,以及如何克服其中一些挑战,将有助于指导针对B细胞起源的恶性肿瘤以及其他血液系统和非血液系统癌症的CAR-T细胞疗法的发展。

相似文献

[1]
Chimeric Antigen Receptor (CAR) T Cells: Lessons Learned from Targeting of CD19 in B-Cell Malignancies.

Drugs. 2017-3

[2]
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[3]
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[4]
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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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Clin Adv Hematol Oncol. 2016-10

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本文引用的文献

[1]
Optimizing Chimeric Antigen Receptor T-Cell Therapy for Adults With Acute Lymphoblastic Leukemia.

J Clin Oncol. 2019-12-9

[2]
Autologous CD19-Targeted CAR T Cells in Patients with Residual CLL following Initial Purine Analog-Based Therapy.

Mol Ther. 2018-6-15

[3]
Immunotherapy of non-Hodgkin's lymphoma with a defined ratio of CD8+ and CD4+ CD19-specific chimeric antigen receptor-modified T cells.

Sci Transl Med. 2016-9-7

[4]
Review: Current clinical applications of chimeric antigen receptor (CAR) modified T cells.

Cytotherapy. 2016-11

[5]
Human CAR T cells with cell-intrinsic PD-1 checkpoint blockade resist tumor-mediated inhibition.

J Clin Invest. 2016-8-1

[6]
CD19-targeted CAR T-cell therapeutics for hematologic malignancies: interpreting clinical outcomes to date.

Blood. 2016-6-30

[7]
CD19 CAR-T cells of defined CD4+:CD8+ composition in adult B cell ALL patients.

J Clin Invest. 2016-6-1

[8]
Identification of Predictive Biomarkers for Cytokine Release Syndrome after Chimeric Antigen Receptor T-cell Therapy for Acute Lymphoblastic Leukemia.

Cancer Discov. 2016-6

[9]
T Cells Expressing CD19/CD20 Bispecific Chimeric Antigen Receptors Prevent Antigen Escape by Malignant B Cells.

Cancer Immunol Res. 2016-4-8

[10]
GD2-specific CAR T Cells Undergo Potent Activation and Deletion Following Antigen Encounter but can be Protected From Activation-induced Cell Death by PD-1 Blockade.

Mol Ther. 2016-6

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