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Lessons learned from a highly-active CD22-specific chimeric antigen receptor
CD22 is an attractive target for the development of immunotherapeutic approaches for the therapy of B-cell malignancies. In particular, an m971 antibody-derived, second generation chimeric antigen receptor (CAR) that targets CD22 holds significant therapeutic promise. The key aspect for the developm...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654586/ https://www.ncbi.nlm.nih.gov/pubmed/23734316 http://dx.doi.org/10.4161/onci.23621 |
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author | Long, Adrienne H. Haso, Waleed M. Orentas, Rimas J. |
author_facet | Long, Adrienne H. Haso, Waleed M. Orentas, Rimas J. |
author_sort | Long, Adrienne H. |
collection | PubMed |
description | CD22 is an attractive target for the development of immunotherapeutic approaches for the therapy of B-cell malignancies. In particular, an m971 antibody-derived, second generation chimeric antigen receptor (CAR) that targets CD22 holds significant therapeutic promise. The key aspect for the development of such a highly-active CAR was its ability to target a membrane-proximal epitope of CD22. |
format | Online Article Text |
id | pubmed-3654586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-36545862013-06-03 Lessons learned from a highly-active CD22-specific chimeric antigen receptor Long, Adrienne H. Haso, Waleed M. Orentas, Rimas J. Oncoimmunology Author's View CD22 is an attractive target for the development of immunotherapeutic approaches for the therapy of B-cell malignancies. In particular, an m971 antibody-derived, second generation chimeric antigen receptor (CAR) that targets CD22 holds significant therapeutic promise. The key aspect for the development of such a highly-active CAR was its ability to target a membrane-proximal epitope of CD22. Landes Bioscience 2013-04-01 2013-04-01 /pmc/articles/PMC3654586/ /pubmed/23734316 http://dx.doi.org/10.4161/onci.23621 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Author's View Long, Adrienne H. Haso, Waleed M. Orentas, Rimas J. Lessons learned from a highly-active CD22-specific chimeric antigen receptor |
title | Lessons learned from a highly-active CD22-specific chimeric antigen receptor |
title_full | Lessons learned from a highly-active CD22-specific chimeric antigen receptor |
title_fullStr | Lessons learned from a highly-active CD22-specific chimeric antigen receptor |
title_full_unstemmed | Lessons learned from a highly-active CD22-specific chimeric antigen receptor |
title_short | Lessons learned from a highly-active CD22-specific chimeric antigen receptor |
title_sort | lessons learned from a highly-active cd22-specific chimeric antigen receptor |
topic | Author's View |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654586/ https://www.ncbi.nlm.nih.gov/pubmed/23734316 http://dx.doi.org/10.4161/onci.23621 |
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