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Chimeric Antigen Receptor-Modified T Cell Therapy in Multiple Myeloma: Beyond B Cell Maturation Antigen
Chimeric antigen receptor (CAR)-modified T cell therapy is a rapidly emerging immunotherapeutic approach that is revolutionizing cancer treatment. The impressive clinical results obtained with CAR-T cell therapy in patients with acute lymphoblastic leukemia and lymphoma have fueled the development o...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646459/ https://www.ncbi.nlm.nih.gov/pubmed/31379824 http://dx.doi.org/10.3389/fimmu.2019.01613 |
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author | Timmers, Marijke Roex, Gils Wang, Yuedi Campillo-Davo, Diana Van Tendeloo, Viggo F. I. Chu, Yiwei Berneman, Zwi N. Luo, Feifei Van Acker, Heleen H. Anguille, Sébastien |
author_facet | Timmers, Marijke Roex, Gils Wang, Yuedi Campillo-Davo, Diana Van Tendeloo, Viggo F. I. Chu, Yiwei Berneman, Zwi N. Luo, Feifei Van Acker, Heleen H. Anguille, Sébastien |
author_sort | Timmers, Marijke |
collection | PubMed |
description | Chimeric antigen receptor (CAR)-modified T cell therapy is a rapidly emerging immunotherapeutic approach that is revolutionizing cancer treatment. The impressive clinical results obtained with CAR-T cell therapy in patients with acute lymphoblastic leukemia and lymphoma have fueled the development of CAR-T cells targeting other malignancies, including multiple myeloma (MM). The field of CAR-T cell therapy for MM is still in its infancy, but remains promising. To date, most studies have been performed with B cell maturation antigen (BCMA)-targeted CARs, for which high response rates have been obtained in early-phase clinical trials. However, responses are usually temporary, and relapses have frequently been observed. One of the major reasons for relapse is the loss or downregulation of BCMA expression following CAR-T therapy. This has fostered a search for alternative target antigens that are expressed on the MM cell surface. In this review, we provide an overview of myeloma target antigens other than BCMA that are currently being evaluated in pre-clinical and clinical studies. |
format | Online Article Text |
id | pubmed-6646459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66464592019-08-02 Chimeric Antigen Receptor-Modified T Cell Therapy in Multiple Myeloma: Beyond B Cell Maturation Antigen Timmers, Marijke Roex, Gils Wang, Yuedi Campillo-Davo, Diana Van Tendeloo, Viggo F. I. Chu, Yiwei Berneman, Zwi N. Luo, Feifei Van Acker, Heleen H. Anguille, Sébastien Front Immunol Immunology Chimeric antigen receptor (CAR)-modified T cell therapy is a rapidly emerging immunotherapeutic approach that is revolutionizing cancer treatment. The impressive clinical results obtained with CAR-T cell therapy in patients with acute lymphoblastic leukemia and lymphoma have fueled the development of CAR-T cells targeting other malignancies, including multiple myeloma (MM). The field of CAR-T cell therapy for MM is still in its infancy, but remains promising. To date, most studies have been performed with B cell maturation antigen (BCMA)-targeted CARs, for which high response rates have been obtained in early-phase clinical trials. However, responses are usually temporary, and relapses have frequently been observed. One of the major reasons for relapse is the loss or downregulation of BCMA expression following CAR-T therapy. This has fostered a search for alternative target antigens that are expressed on the MM cell surface. In this review, we provide an overview of myeloma target antigens other than BCMA that are currently being evaluated in pre-clinical and clinical studies. Frontiers Media S.A. 2019-07-16 /pmc/articles/PMC6646459/ /pubmed/31379824 http://dx.doi.org/10.3389/fimmu.2019.01613 Text en Copyright © 2019 Timmers, Roex, Wang, Campillo-Davo, Van Tendeloo, Chu, Berneman, Luo, Van Acker and Anguille. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Timmers, Marijke Roex, Gils Wang, Yuedi Campillo-Davo, Diana Van Tendeloo, Viggo F. I. Chu, Yiwei Berneman, Zwi N. Luo, Feifei Van Acker, Heleen H. Anguille, Sébastien Chimeric Antigen Receptor-Modified T Cell Therapy in Multiple Myeloma: Beyond B Cell Maturation Antigen |
title | Chimeric Antigen Receptor-Modified T Cell Therapy in Multiple Myeloma: Beyond B Cell Maturation Antigen |
title_full | Chimeric Antigen Receptor-Modified T Cell Therapy in Multiple Myeloma: Beyond B Cell Maturation Antigen |
title_fullStr | Chimeric Antigen Receptor-Modified T Cell Therapy in Multiple Myeloma: Beyond B Cell Maturation Antigen |
title_full_unstemmed | Chimeric Antigen Receptor-Modified T Cell Therapy in Multiple Myeloma: Beyond B Cell Maturation Antigen |
title_short | Chimeric Antigen Receptor-Modified T Cell Therapy in Multiple Myeloma: Beyond B Cell Maturation Antigen |
title_sort | chimeric antigen receptor-modified t cell therapy in multiple myeloma: beyond b cell maturation antigen |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646459/ https://www.ncbi.nlm.nih.gov/pubmed/31379824 http://dx.doi.org/10.3389/fimmu.2019.01613 |
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