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Chimeric Antigen Receptor T-Cell Therapy for Multiple Myeloma

CD19 Chimeric antigen receptor (CAR) T cell therapy has been shown to be effective for B cell leukemia and lymphoma. Many researchers are now trying to develop CAR T cells for various types of cancer. For multiple myeloma (MM), B-cell maturation antigen (BCMA) has been recently proved to be a promis...

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Detalles Bibliográficos
Autor principal: Hosen, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966463/
https://www.ncbi.nlm.nih.gov/pubmed/31847470
http://dx.doi.org/10.3390/cancers11122024
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author Hosen, Naoki
author_facet Hosen, Naoki
author_sort Hosen, Naoki
collection PubMed
description CD19 Chimeric antigen receptor (CAR) T cell therapy has been shown to be effective for B cell leukemia and lymphoma. Many researchers are now trying to develop CAR T cells for various types of cancer. For multiple myeloma (MM), B-cell maturation antigen (BCMA) has been recently proved to be a promising target. However, cure of MM is still difficult, and several other targets, for example immunoglobulin kappa chain, SLAM Family Member 7 (SLAMF7), or G-protein coupled receptor family C group 5 member D (GPRC5D), are being tested as targets for CAR T cells. We also reported that the activated integrin β7 can serve as a specific target for CAR T cells against MM, and are preparing a clinical trial. In this review, we summarized current status of CAR T cell therapy for MM and discussed about the future perspectives.
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spelling pubmed-69664632020-01-27 Chimeric Antigen Receptor T-Cell Therapy for Multiple Myeloma Hosen, Naoki Cancers (Basel) Review CD19 Chimeric antigen receptor (CAR) T cell therapy has been shown to be effective for B cell leukemia and lymphoma. Many researchers are now trying to develop CAR T cells for various types of cancer. For multiple myeloma (MM), B-cell maturation antigen (BCMA) has been recently proved to be a promising target. However, cure of MM is still difficult, and several other targets, for example immunoglobulin kappa chain, SLAM Family Member 7 (SLAMF7), or G-protein coupled receptor family C group 5 member D (GPRC5D), are being tested as targets for CAR T cells. We also reported that the activated integrin β7 can serve as a specific target for CAR T cells against MM, and are preparing a clinical trial. In this review, we summarized current status of CAR T cell therapy for MM and discussed about the future perspectives. MDPI 2019-12-15 /pmc/articles/PMC6966463/ /pubmed/31847470 http://dx.doi.org/10.3390/cancers11122024 Text en © 2019 by the author. 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
Hosen, Naoki
Chimeric Antigen Receptor T-Cell Therapy for Multiple Myeloma
title Chimeric Antigen Receptor T-Cell Therapy for Multiple Myeloma
title_full Chimeric Antigen Receptor T-Cell Therapy for Multiple Myeloma
title_fullStr Chimeric Antigen Receptor T-Cell Therapy for Multiple Myeloma
title_full_unstemmed Chimeric Antigen Receptor T-Cell Therapy for Multiple Myeloma
title_short Chimeric Antigen Receptor T-Cell Therapy for Multiple Myeloma
title_sort chimeric antigen receptor t-cell therapy for multiple myeloma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966463/
https://www.ncbi.nlm.nih.gov/pubmed/31847470
http://dx.doi.org/10.3390/cancers11122024
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