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Anti-CD19 CAR T cells potently redirected to kill solid tumor cells
Successful CAR T cell therapy for the treatment of solid tumors requires exemplary CAR T cell expansion, persistence and fitness, and the ability to target tumor antigens safely. Here we address this constellation of critical attributes for successful cellular therapy by using integrated technologie...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971483/ https://www.ncbi.nlm.nih.gov/pubmed/33735268 http://dx.doi.org/10.1371/journal.pone.0247701 |
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author | Ambrose, Christine Su, Lihe Wu, Lan Dufort, Fay J. Sanford, Thomas Birt, Alyssa Hackel, Benjamin J. Hombach, Andreas Abken, Hinrich Lobb, Roy R. Rennert, Paul D. |
author_facet | Ambrose, Christine Su, Lihe Wu, Lan Dufort, Fay J. Sanford, Thomas Birt, Alyssa Hackel, Benjamin J. Hombach, Andreas Abken, Hinrich Lobb, Roy R. Rennert, Paul D. |
author_sort | Ambrose, Christine |
collection | PubMed |
description | Successful CAR T cell therapy for the treatment of solid tumors requires exemplary CAR T cell expansion, persistence and fitness, and the ability to target tumor antigens safely. Here we address this constellation of critical attributes for successful cellular therapy by using integrated technologies that simplify development and derisk clinical translation. We have developed a CAR-CD19 T cell that secretes a CD19-anti-Her2 bridging protein. This cell therapy strategy exploits the ability of CD19-targeting CAR T cells to interact with CD19 on normal B cells to drive expansion, persistence and fitness. The secreted bridging protein potently binds to Her2-positive tumor cells, mediating CAR-CD19 T cell cytotoxicity in vitro and in vivo. Because of its short half-life, the secreted bridging protein will selectively accumulate at the site of highest antigen expression, ie. at the tumor. Bridging proteins that bind to multiple different tumor antigens have been created. Therefore, antigen-bridging CAR-CD19 T cells incorporate critical attributes for successful solid tumor cell therapy. This platform can be exploited to attack tumor antigens on any cancer. |
format | Online Article Text |
id | pubmed-7971483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-79714832021-03-31 Anti-CD19 CAR T cells potently redirected to kill solid tumor cells Ambrose, Christine Su, Lihe Wu, Lan Dufort, Fay J. Sanford, Thomas Birt, Alyssa Hackel, Benjamin J. Hombach, Andreas Abken, Hinrich Lobb, Roy R. Rennert, Paul D. PLoS One Research Article Successful CAR T cell therapy for the treatment of solid tumors requires exemplary CAR T cell expansion, persistence and fitness, and the ability to target tumor antigens safely. Here we address this constellation of critical attributes for successful cellular therapy by using integrated technologies that simplify development and derisk clinical translation. We have developed a CAR-CD19 T cell that secretes a CD19-anti-Her2 bridging protein. This cell therapy strategy exploits the ability of CD19-targeting CAR T cells to interact with CD19 on normal B cells to drive expansion, persistence and fitness. The secreted bridging protein potently binds to Her2-positive tumor cells, mediating CAR-CD19 T cell cytotoxicity in vitro and in vivo. Because of its short half-life, the secreted bridging protein will selectively accumulate at the site of highest antigen expression, ie. at the tumor. Bridging proteins that bind to multiple different tumor antigens have been created. Therefore, antigen-bridging CAR-CD19 T cells incorporate critical attributes for successful solid tumor cell therapy. This platform can be exploited to attack tumor antigens on any cancer. Public Library of Science 2021-03-18 /pmc/articles/PMC7971483/ /pubmed/33735268 http://dx.doi.org/10.1371/journal.pone.0247701 Text en © 2021 Ambrose et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Ambrose, Christine Su, Lihe Wu, Lan Dufort, Fay J. Sanford, Thomas Birt, Alyssa Hackel, Benjamin J. Hombach, Andreas Abken, Hinrich Lobb, Roy R. Rennert, Paul D. Anti-CD19 CAR T cells potently redirected to kill solid tumor cells |
title | Anti-CD19 CAR T cells potently redirected to kill solid tumor cells |
title_full | Anti-CD19 CAR T cells potently redirected to kill solid tumor cells |
title_fullStr | Anti-CD19 CAR T cells potently redirected to kill solid tumor cells |
title_full_unstemmed | Anti-CD19 CAR T cells potently redirected to kill solid tumor cells |
title_short | Anti-CD19 CAR T cells potently redirected to kill solid tumor cells |
title_sort | anti-cd19 car t cells potently redirected to kill solid tumor cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971483/ https://www.ncbi.nlm.nih.gov/pubmed/33735268 http://dx.doi.org/10.1371/journal.pone.0247701 |
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