Literature DB >> 27040708

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

Joseph A Fraietta1, Robert D Schwab1, Marcela V Maus2.   

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.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CAR; CLL; Immunotherapy; Leukemia; T cell

Mesh:

Substances:

Year:  2016        PMID: 27040708      PMCID: PMC4824551          DOI: 10.1053/j.seminoncol.2016.02.006

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


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  7 in total

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