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The expansion of targetable biomarkers for CAR T cell therapy

Biomarkers are an integral part of cancer management due to their use in risk assessment, screening, differential diagnosis, prognosis, prediction of response to treatment, and monitoring progress of disease. Recently, with the advent of Chimeric Antigen Receptor (CAR) T cell therapy, a new category...

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Autores principales: Townsend, Michelle H., Shrestha, Gajendra, Robison, Richard A., O’Neill, Kim L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054736/
https://www.ncbi.nlm.nih.gov/pubmed/30031396
http://dx.doi.org/10.1186/s13046-018-0817-0
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author Townsend, Michelle H.
Shrestha, Gajendra
Robison, Richard A.
O’Neill, Kim L.
author_facet Townsend, Michelle H.
Shrestha, Gajendra
Robison, Richard A.
O’Neill, Kim L.
author_sort Townsend, Michelle H.
collection PubMed
description Biomarkers are an integral part of cancer management due to their use in risk assessment, screening, differential diagnosis, prognosis, prediction of response to treatment, and monitoring progress of disease. Recently, with the advent of Chimeric Antigen Receptor (CAR) T cell therapy, a new category of targetable biomarkers has emerged. These biomarkers are associated with the surface of malignant cells and serve as targets for directing cytotoxic T cells. The first biomarker target used for CAR T cell therapy was CD19, a B cell marker expressed highly on malignant B cells. With the success of CD19, the last decade has shown an explosion of new targetable biomarkers on a range of human malignancies. These surface targets have made it possible to provide directed, specific therapy that reduces healthy tissue destruction and preserves the patient’s immune system during treatment. As of May 2018, there are over 100 clinical trials underway that target over 25 different surface biomarkers in almost every human tissue. This expansion has led to not only promising results in terms of patient outcome, but has also led to an exponential growth in the investigation of new biomarkers that could potentially be utilized in CAR T cell therapy for treating patients. In this review, we discuss the biomarkers currently under investigation and point out several promising biomarkers in the preclinical stage of development that may be useful as targets.
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spelling pubmed-60547362018-07-23 The expansion of targetable biomarkers for CAR T cell therapy Townsend, Michelle H. Shrestha, Gajendra Robison, Richard A. O’Neill, Kim L. J Exp Clin Cancer Res Review Biomarkers are an integral part of cancer management due to their use in risk assessment, screening, differential diagnosis, prognosis, prediction of response to treatment, and monitoring progress of disease. Recently, with the advent of Chimeric Antigen Receptor (CAR) T cell therapy, a new category of targetable biomarkers has emerged. These biomarkers are associated with the surface of malignant cells and serve as targets for directing cytotoxic T cells. The first biomarker target used for CAR T cell therapy was CD19, a B cell marker expressed highly on malignant B cells. With the success of CD19, the last decade has shown an explosion of new targetable biomarkers on a range of human malignancies. These surface targets have made it possible to provide directed, specific therapy that reduces healthy tissue destruction and preserves the patient’s immune system during treatment. As of May 2018, there are over 100 clinical trials underway that target over 25 different surface biomarkers in almost every human tissue. This expansion has led to not only promising results in terms of patient outcome, but has also led to an exponential growth in the investigation of new biomarkers that could potentially be utilized in CAR T cell therapy for treating patients. In this review, we discuss the biomarkers currently under investigation and point out several promising biomarkers in the preclinical stage of development that may be useful as targets. BioMed Central 2018-07-21 /pmc/articles/PMC6054736/ /pubmed/30031396 http://dx.doi.org/10.1186/s13046-018-0817-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Townsend, Michelle H.
Shrestha, Gajendra
Robison, Richard A.
O’Neill, Kim L.
The expansion of targetable biomarkers for CAR T cell therapy
title The expansion of targetable biomarkers for CAR T cell therapy
title_full The expansion of targetable biomarkers for CAR T cell therapy
title_fullStr The expansion of targetable biomarkers for CAR T cell therapy
title_full_unstemmed The expansion of targetable biomarkers for CAR T cell therapy
title_short The expansion of targetable biomarkers for CAR T cell therapy
title_sort expansion of targetable biomarkers for car t cell therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054736/
https://www.ncbi.nlm.nih.gov/pubmed/30031396
http://dx.doi.org/10.1186/s13046-018-0817-0
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