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Innovation in BCMA CAR-T therapy: Building beyond the Model T
Autologous chimeric antigen receptor T-cell (CAR-T) therapies targeting B-cell maturation antigen (BCMA) have revolutionized the field of multiple myeloma in the same way that the Ford Model T revolutionized the original CAR world a century ago. However, we are only beginning to understand how to im...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729952/ https://www.ncbi.nlm.nih.gov/pubmed/36505779 http://dx.doi.org/10.3389/fonc.2022.1070353 |
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author | Banerjee, Rahul Lee, Sarah S. Cowan, Andrew J. |
author_facet | Banerjee, Rahul Lee, Sarah S. Cowan, Andrew J. |
author_sort | Banerjee, Rahul |
collection | PubMed |
description | Autologous chimeric antigen receptor T-cell (CAR-T) therapies targeting B-cell maturation antigen (BCMA) have revolutionized the field of multiple myeloma in the same way that the Ford Model T revolutionized the original CAR world a century ago. However, we are only beginning to understand how to improve the efficacy and usability of these cellular therapies. In this review, we explore three automotive analogies for innovation with BCMA CAR-T therapies: stronger engines, better mileage, and hassle-free delivery. Firstly, we can build stronger engines in terms of BCMA targeting: improved antigen binding, tools to modulate antigen density, and armoring to better reach the antigen itself. Secondly, we can improve “mileage” in terms of response durability through ex vivo CAR design and in vivo immune manipulation. Thirdly, we can implement hassle-free delivery through rapid manufacturing protocols and off-the-shelf products. Just as the Model T set a benchmark for car manufacturing over 100 years ago, idecabtagene vicleucel and ciltacabtagene autoleucel have now set the starting point for BCMA CAR-T therapy with their approvals. As with any emerging technology, whether automotive or cellular, the best in innovation and optimization is yet to come. |
format | Online Article Text |
id | pubmed-9729952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97299522022-12-09 Innovation in BCMA CAR-T therapy: Building beyond the Model T Banerjee, Rahul Lee, Sarah S. Cowan, Andrew J. Front Oncol Oncology Autologous chimeric antigen receptor T-cell (CAR-T) therapies targeting B-cell maturation antigen (BCMA) have revolutionized the field of multiple myeloma in the same way that the Ford Model T revolutionized the original CAR world a century ago. However, we are only beginning to understand how to improve the efficacy and usability of these cellular therapies. In this review, we explore three automotive analogies for innovation with BCMA CAR-T therapies: stronger engines, better mileage, and hassle-free delivery. Firstly, we can build stronger engines in terms of BCMA targeting: improved antigen binding, tools to modulate antigen density, and armoring to better reach the antigen itself. Secondly, we can improve “mileage” in terms of response durability through ex vivo CAR design and in vivo immune manipulation. Thirdly, we can implement hassle-free delivery through rapid manufacturing protocols and off-the-shelf products. Just as the Model T set a benchmark for car manufacturing over 100 years ago, idecabtagene vicleucel and ciltacabtagene autoleucel have now set the starting point for BCMA CAR-T therapy with their approvals. As with any emerging technology, whether automotive or cellular, the best in innovation and optimization is yet to come. Frontiers Media S.A. 2022-11-24 /pmc/articles/PMC9729952/ /pubmed/36505779 http://dx.doi.org/10.3389/fonc.2022.1070353 Text en Copyright © 2022 Banerjee, Lee and Cowan https://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 | Oncology Banerjee, Rahul Lee, Sarah S. Cowan, Andrew J. Innovation in BCMA CAR-T therapy: Building beyond the Model T |
title | Innovation in BCMA CAR-T therapy: Building beyond the Model T |
title_full | Innovation in BCMA CAR-T therapy: Building beyond the Model T |
title_fullStr | Innovation in BCMA CAR-T therapy: Building beyond the Model T |
title_full_unstemmed | Innovation in BCMA CAR-T therapy: Building beyond the Model T |
title_short | Innovation in BCMA CAR-T therapy: Building beyond the Model T |
title_sort | innovation in bcma car-t therapy: building beyond the model t |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729952/ https://www.ncbi.nlm.nih.gov/pubmed/36505779 http://dx.doi.org/10.3389/fonc.2022.1070353 |
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