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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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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. |
format | Online Article Text |
id | pubmed-9327123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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