CAR T-cell therapy: Balance of efficacy and safety


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Abstract

Early results from clinical trials of autologous chimeric antigen receptor (CAR)-expressing T cells for the therapy of B-cell malignancies have encouraged extending the potency of this therapy to other cancers. However, the success of using CAR T-cells to treat patients with solid tumors has been limited. In this review, we summarize current knowledge on the design and applications of CARs for the targeted therapy of cancer. We describe existing issues that limit the widespread application of CAR T cells and discuss the optimization steps needed to further improve safety and efficacy of this therapeutic platform.

About the authors

S. V. Kulemzin

Institute of Molecular and Cellular Biology

Email: gorchakov@mcb.nsc.ru
Russian Federation, Novosibirsk, 630090

V. V. Kuznetsova

Institute of Molecular and Cellular Biology

Email: gorchakov@mcb.nsc.ru
Russian Federation, Novosibirsk, 630090

M. Mamonkin

Center for Cell and Gene Therapy, Baylor College of Medicine

Email: gorchakov@mcb.nsc.ru
United States, Houston, TX

A. V. Taranin

Institute of Molecular and Cellular Biology; Novosibirsk State University

Email: gorchakov@mcb.nsc.ru
Russian Federation, Novosibirsk, 630090; Novosibirsk, 630090

A. A. Gorchakov

Institute of Molecular and Cellular Biology; Novosibirsk State University

Author for correspondence.
Email: gorchakov@mcb.nsc.ru
Russian Federation, Novosibirsk, 630090; Novosibirsk, 630090

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