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Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy

The development of novel chimeric antigen receptor (CAR) cell therapies is rapidly growing, with 299 new agents being reported and 109 new clinical trials initiated so far this year. One critical lesson from approved CD19-specific CAR therapies is that target isoform switching has been shown to caus...

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Detalles Bibliográficos
Autores principales: Bogetofte Barnkob, Mike, Vitting-Seerup, Kristoffer, Rønn Olsen, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327123/
https://www.ncbi.nlm.nih.gov/pubmed/35919495
http://dx.doi.org/10.1093/immadv/ltac009
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author Bogetofte Barnkob, Mike
Vitting-Seerup, Kristoffer
Rønn Olsen, Lars
author_facet Bogetofte Barnkob, Mike
Vitting-Seerup, Kristoffer
Rønn Olsen, Lars
author_sort Bogetofte Barnkob, Mike
collection PubMed
description The development of novel chimeric antigen receptor (CAR) cell therapies is rapidly growing, with 299 new agents being reported and 109 new clinical trials initiated so far this year. One critical lesson from approved CD19-specific CAR therapies is that target isoform switching has been shown to cause tumour relapse, but little is known about the isoforms of CAR targets in solid cancers. Here we assess the protein isoform landscape and identify both the challenges and opportunities protein isoform switching present as CAR therapy is applied to solid cancers.
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spelling pubmed-93271232022-08-01 Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy Bogetofte Barnkob, Mike Vitting-Seerup, Kristoffer Rønn Olsen, Lars Immunother Adv Commentary The development of novel chimeric antigen receptor (CAR) cell therapies is rapidly growing, with 299 new agents being reported and 109 new clinical trials initiated so far this year. One critical lesson from approved CD19-specific CAR therapies is that target isoform switching has been shown to cause tumour relapse, but little is known about the isoforms of CAR targets in solid cancers. Here we assess the protein isoform landscape and identify both the challenges and opportunities protein isoform switching present as CAR therapy is applied to solid cancers. Oxford University Press 2022-04-20 /pmc/articles/PMC9327123/ /pubmed/35919495 http://dx.doi.org/10.1093/immadv/ltac009 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Immunology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Commentary
Bogetofte Barnkob, Mike
Vitting-Seerup, Kristoffer
Rønn Olsen, Lars
Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy
title Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy
title_full Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy
title_fullStr Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy
title_full_unstemmed Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy
title_short Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy
title_sort target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9327123/
https://www.ncbi.nlm.nih.gov/pubmed/35919495
http://dx.doi.org/10.1093/immadv/ltac009
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