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Chimeric antigen receptor T cell therapy for multiple myeloma

Chimeric antigen receptor (CAR) T cell therapy is a new cancer immunotherapy targeting cancer-specific cell surface antigen. CD19-CAR T cells have been already shown to be very effective to B cell leukemia/lymphoma. Now, many researchers are developing CAR T cells for multiple myeloma. CAR T cells t...

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Detalles Bibliográficos
Autores principales: Hasegawa, Kana, Hosen, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547554/
https://www.ncbi.nlm.nih.gov/pubmed/31171941
http://dx.doi.org/10.1186/s41232-019-0100-6
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author Hasegawa, Kana
Hosen, Naoki
author_facet Hasegawa, Kana
Hosen, Naoki
author_sort Hasegawa, Kana
collection PubMed
description Chimeric antigen receptor (CAR) T cell therapy is a new cancer immunotherapy targeting cancer-specific cell surface antigen. CD19-CAR T cells have been already shown to be very effective to B cell leukemia/lymphoma. Now, many researchers are developing CAR T cells for multiple myeloma. CAR T cells targeting B cell maturation antigen (BCMA) showed promising efficacy in early phase clinical trials. We have recently reported that CAR T cells targeting the activated integrin β7 can selectively eradicate MM cells including CD19(+) clonotypic B cells and are preparing a clinical trial.
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spelling pubmed-65475542019-06-06 Chimeric antigen receptor T cell therapy for multiple myeloma Hasegawa, Kana Hosen, Naoki Inflamm Regen Review Chimeric antigen receptor (CAR) T cell therapy is a new cancer immunotherapy targeting cancer-specific cell surface antigen. CD19-CAR T cells have been already shown to be very effective to B cell leukemia/lymphoma. Now, many researchers are developing CAR T cells for multiple myeloma. CAR T cells targeting B cell maturation antigen (BCMA) showed promising efficacy in early phase clinical trials. We have recently reported that CAR T cells targeting the activated integrin β7 can selectively eradicate MM cells including CD19(+) clonotypic B cells and are preparing a clinical trial. BioMed Central 2019-06-04 /pmc/articles/PMC6547554/ /pubmed/31171941 http://dx.doi.org/10.1186/s41232-019-0100-6 Text en © The Author(s) 2019 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
Hasegawa, Kana
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/PMC6547554/
https://www.ncbi.nlm.nih.gov/pubmed/31171941
http://dx.doi.org/10.1186/s41232-019-0100-6
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