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Improving therapy of chronic lymphocytic leukemia with chimeric antigen receptor T cells.

作者信息

Fraietta Joseph A, Schwab Robert D, Maus Marcela V

机构信息

Center for Cellular Immunotherapy, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA.

Cellular Immunotherapy Program, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA.

出版信息

Semin Oncol. 2016 Apr;43(2):291-9. doi: 10.1053/j.seminoncol.2016.02.006. Epub 2016 Feb 9.


DOI:10.1053/j.seminoncol.2016.02.006
PMID:27040708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4824551/
Abstract

Adoptive cell immunotherapy for the treatment of chronic lymphocytic leukemia (CLL) has heralded a new era of synthetic biology. The infusion of genetically engineered, autologous chimeric antigen receptor (CAR) T cells directed against CD19 expressed by normal and malignant B cells represents a novel approach to cancer therapy. The results of recent clinical trials of CAR T cells in relapsed and refractory CLL have demonstrated long-term disease-free remissions, underscoring the power of harnessing and redirecting the immune system against cancer. This review will briefly summarize T-cell therapies in development for CLL disease. We discuss the role of T-cell function and phenotype, T-cell culture optimization, CAR design, and approaches to potentiate the survival and anti-tumor effects of infused lymphocytes. Future efforts will focus on improving the efficacy of CAR T cells for the treatment of CLL and incorporating adoptive cell immunotherapy into standard medical management of CLL.

摘要

相似文献

[1]
Improving therapy of chronic lymphocytic leukemia with chimeric antigen receptor T cells.

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本文引用的文献

[1]
Chimeric antigen receptor T cells persist and induce sustained remissions in relapsed refractory chronic lymphocytic leukemia.

Sci Transl Med. 2015-9-2

[2]
CD19-targeted chimeric antigen receptor T-cell therapy for acute lymphoblastic leukemia.

Blood. 2015-6-25

[3]
miR-155 augments CD8+ T-cell antitumor activity in lymphoreplete hosts by enhancing responsiveness to homeostatic γc cytokines.

Proc Natl Acad Sci U S A. 2015-1-13

[4]
Transplant for CLL: still an option?

Blood. 2014-12-18

[5]
Target antigen density governs the efficacy of anti-CD20-CD28-CD3 ζ chimeric antigen receptor-modified effector CD8+ T cells.

J Immunol. 2015-2-1

[6]
Bruton's tyrosine kinase inhibitors and their clinical potential in the treatment of B-cell malignancies: focus on ibrutinib.

Ther Adv Hematol. 2014-8

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N Engl J Med. 2014-10-16

[8]
Managing high-risk CLL during transition to a new treatment era: stem cell transplantation or novel agents?

Blood. 2014-12-18

[9]
ICOS-based chimeric antigen receptors program bipolar TH17/TH1 cells.

Blood. 2014-8-14

[10]
Paving the road to MRD-guided treatment in CLL.

Blood. 2014-6-12

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