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You Have Got a Fast CAR: Chimeric Antigen Receptor NK Cells in Cancer Therapy

The clinical success stories of chimeric antigen receptor (CAR)-T cell therapy against B-cell malignancies have contributed to immunotherapy being at the forefront of cancer therapy today. Their success has fueled interest in improving CAR constructs, identifying additional antigens to target, and c...

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Detalles Bibliográficos
Autores principales: Pfefferle, Aline, Huntington, Nicholas D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140022/
https://www.ncbi.nlm.nih.gov/pubmed/32192067
http://dx.doi.org/10.3390/cancers12030706
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author Pfefferle, Aline
Huntington, Nicholas D.
author_facet Pfefferle, Aline
Huntington, Nicholas D.
author_sort Pfefferle, Aline
collection PubMed
description The clinical success stories of chimeric antigen receptor (CAR)-T cell therapy against B-cell malignancies have contributed to immunotherapy being at the forefront of cancer therapy today. Their success has fueled interest in improving CAR constructs, identifying additional antigens to target, and clinically evaluating them across a wide range of malignancies. However, along with the exciting potential of CAR-T therapy comes the real possibility of serious side effects. While the FDA has approved commercialized CAR-T cell therapy, challenges associated with manufacturing, costs, and related toxicities have resulted in increased attention being paid to implementing CAR technology in innate cytotoxic natural killer (NK) cells. Here, we review the current landscape of the CAR-NK field, from successful clinical implementation to outstanding challenges which remain to be addressed to deliver the full potential of this therapy to more patients.
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spelling pubmed-71400222020-04-13 You Have Got a Fast CAR: Chimeric Antigen Receptor NK Cells in Cancer Therapy Pfefferle, Aline Huntington, Nicholas D. Cancers (Basel) Review The clinical success stories of chimeric antigen receptor (CAR)-T cell therapy against B-cell malignancies have contributed to immunotherapy being at the forefront of cancer therapy today. Their success has fueled interest in improving CAR constructs, identifying additional antigens to target, and clinically evaluating them across a wide range of malignancies. However, along with the exciting potential of CAR-T therapy comes the real possibility of serious side effects. While the FDA has approved commercialized CAR-T cell therapy, challenges associated with manufacturing, costs, and related toxicities have resulted in increased attention being paid to implementing CAR technology in innate cytotoxic natural killer (NK) cells. Here, we review the current landscape of the CAR-NK field, from successful clinical implementation to outstanding challenges which remain to be addressed to deliver the full potential of this therapy to more patients. MDPI 2020-03-17 /pmc/articles/PMC7140022/ /pubmed/32192067 http://dx.doi.org/10.3390/cancers12030706 Text en © 2020 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
Pfefferle, Aline
Huntington, Nicholas D.
You Have Got a Fast CAR: Chimeric Antigen Receptor NK Cells in Cancer Therapy
title You Have Got a Fast CAR: Chimeric Antigen Receptor NK Cells in Cancer Therapy
title_full You Have Got a Fast CAR: Chimeric Antigen Receptor NK Cells in Cancer Therapy
title_fullStr You Have Got a Fast CAR: Chimeric Antigen Receptor NK Cells in Cancer Therapy
title_full_unstemmed You Have Got a Fast CAR: Chimeric Antigen Receptor NK Cells in Cancer Therapy
title_short You Have Got a Fast CAR: Chimeric Antigen Receptor NK Cells in Cancer Therapy
title_sort you have got a fast car: chimeric antigen receptor nk cells in cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140022/
https://www.ncbi.nlm.nih.gov/pubmed/32192067
http://dx.doi.org/10.3390/cancers12030706
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