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Incorporation of Immune Checkpoint Blockade into Chimeric Antigen Receptor T Cells (CAR-Ts): Combination or Built-In CAR-T

Chimeric antigen receptor (CAR) T cell therapy represents the first U.S. Food and Drug Administration approved gene therapy and these engineered cells function with unprecedented efficacy in the treatment of refractory CD19 positive hematologic malignancies. CAR translation to solid tumors is also b...

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Detalles Bibliográficos
Autores principales: Yoon, Dok Hyun, Osborn, Mark J., Tolar, Jakub, Kim, Chong Jai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855562/
https://www.ncbi.nlm.nih.gov/pubmed/29364163
http://dx.doi.org/10.3390/ijms19020340
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author Yoon, Dok Hyun
Osborn, Mark J.
Tolar, Jakub
Kim, Chong Jai
author_facet Yoon, Dok Hyun
Osborn, Mark J.
Tolar, Jakub
Kim, Chong Jai
author_sort Yoon, Dok Hyun
collection PubMed
description Chimeric antigen receptor (CAR) T cell therapy represents the first U.S. Food and Drug Administration approved gene therapy and these engineered cells function with unprecedented efficacy in the treatment of refractory CD19 positive hematologic malignancies. CAR translation to solid tumors is also being actively investigated; however, efficacy to date has been variable due to tumor-evolved mechanisms that inhibit local immune cell activity. To bolster the potency of CAR-T cells, modulation of the immunosuppressive tumor microenvironment with immune-checkpoint blockade is a promising strategy. The impact of this approach on hematological malignancies is in its infancy, and in this review we discuss CAR-T cells and their synergy with immune-checkpoint blockade.
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spelling pubmed-58555622018-03-20 Incorporation of Immune Checkpoint Blockade into Chimeric Antigen Receptor T Cells (CAR-Ts): Combination or Built-In CAR-T Yoon, Dok Hyun Osborn, Mark J. Tolar, Jakub Kim, Chong Jai Int J Mol Sci Review Chimeric antigen receptor (CAR) T cell therapy represents the first U.S. Food and Drug Administration approved gene therapy and these engineered cells function with unprecedented efficacy in the treatment of refractory CD19 positive hematologic malignancies. CAR translation to solid tumors is also being actively investigated; however, efficacy to date has been variable due to tumor-evolved mechanisms that inhibit local immune cell activity. To bolster the potency of CAR-T cells, modulation of the immunosuppressive tumor microenvironment with immune-checkpoint blockade is a promising strategy. The impact of this approach on hematological malignancies is in its infancy, and in this review we discuss CAR-T cells and their synergy with immune-checkpoint blockade. MDPI 2018-01-24 /pmc/articles/PMC5855562/ /pubmed/29364163 http://dx.doi.org/10.3390/ijms19020340 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Yoon, Dok Hyun
Osborn, Mark J.
Tolar, Jakub
Kim, Chong Jai
Incorporation of Immune Checkpoint Blockade into Chimeric Antigen Receptor T Cells (CAR-Ts): Combination or Built-In CAR-T
title Incorporation of Immune Checkpoint Blockade into Chimeric Antigen Receptor T Cells (CAR-Ts): Combination or Built-In CAR-T
title_full Incorporation of Immune Checkpoint Blockade into Chimeric Antigen Receptor T Cells (CAR-Ts): Combination or Built-In CAR-T
title_fullStr Incorporation of Immune Checkpoint Blockade into Chimeric Antigen Receptor T Cells (CAR-Ts): Combination or Built-In CAR-T
title_full_unstemmed Incorporation of Immune Checkpoint Blockade into Chimeric Antigen Receptor T Cells (CAR-Ts): Combination or Built-In CAR-T
title_short Incorporation of Immune Checkpoint Blockade into Chimeric Antigen Receptor T Cells (CAR-Ts): Combination or Built-In CAR-T
title_sort incorporation of immune checkpoint blockade into chimeric antigen receptor t cells (car-ts): combination or built-in car-t
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855562/
https://www.ncbi.nlm.nih.gov/pubmed/29364163
http://dx.doi.org/10.3390/ijms19020340
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