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Versatile chimeric antigen receptor platform for controllable and combinatorial T cell therapy
Chimeric antigen receptor (CAR) T cells show remarkable therapeutic effects in some hematological malignancies. However, CAR T cells can also cause life-threatening side effects. In order to minimize off-target and on-target/off-tumor reactions, improve safety, enable controllability, provide high f...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458653/ https://www.ncbi.nlm.nih.gov/pubmed/32923149 http://dx.doi.org/10.1080/2162402X.2020.1785608 |
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author | Feldmann, Anja Hoffmann, Anja Bergmann, Ralf Koristka, Stefanie Berndt, Nicole Arndt, Claudia Rodrigues Loureiro, Liliana Kittel-Boselli, Enrico Mitwasi, Nicola Kegler, Alexandra Lamprecht, Chris González Soto, Karla Elizabeth Bachmann, Michael |
author_facet | Feldmann, Anja Hoffmann, Anja Bergmann, Ralf Koristka, Stefanie Berndt, Nicole Arndt, Claudia Rodrigues Loureiro, Liliana Kittel-Boselli, Enrico Mitwasi, Nicola Kegler, Alexandra Lamprecht, Chris González Soto, Karla Elizabeth Bachmann, Michael |
author_sort | Feldmann, Anja |
collection | PubMed |
description | Chimeric antigen receptor (CAR) T cells show remarkable therapeutic effects in some hematological malignancies. However, CAR T cells can also cause life-threatening side effects. In order to minimize off-target and on-target/off-tumor reactions, improve safety, enable controllability, provide high flexibility, and increase tumor specificity, we established a novel humanized artificial receptor platform termed RevCARs. RevCAR genes encode for small surface receptors lacking any antigen-binding moiety. Steering of RevCAR T cells occurs via bispecific targeting molecules (TMs). The small size of RevCAR-encoding genes allows the construction of polycistronic vectors. Here, we demonstrate that RevCAR T cells efficiently kill tumor cells, can be steered by TMs, flexibly redirected against multiple targets, and used for combinatorial targeting following the “OR” and “AND” gate logic. |
format | Online Article Text |
id | pubmed-7458653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-74586532020-09-11 Versatile chimeric antigen receptor platform for controllable and combinatorial T cell therapy Feldmann, Anja Hoffmann, Anja Bergmann, Ralf Koristka, Stefanie Berndt, Nicole Arndt, Claudia Rodrigues Loureiro, Liliana Kittel-Boselli, Enrico Mitwasi, Nicola Kegler, Alexandra Lamprecht, Chris González Soto, Karla Elizabeth Bachmann, Michael Oncoimmunology Original Research Chimeric antigen receptor (CAR) T cells show remarkable therapeutic effects in some hematological malignancies. However, CAR T cells can also cause life-threatening side effects. In order to minimize off-target and on-target/off-tumor reactions, improve safety, enable controllability, provide high flexibility, and increase tumor specificity, we established a novel humanized artificial receptor platform termed RevCARs. RevCAR genes encode for small surface receptors lacking any antigen-binding moiety. Steering of RevCAR T cells occurs via bispecific targeting molecules (TMs). The small size of RevCAR-encoding genes allows the construction of polycistronic vectors. Here, we demonstrate that RevCAR T cells efficiently kill tumor cells, can be steered by TMs, flexibly redirected against multiple targets, and used for combinatorial targeting following the “OR” and “AND” gate logic. Taylor & Francis 2020-07-03 /pmc/articles/PMC7458653/ /pubmed/32923149 http://dx.doi.org/10.1080/2162402X.2020.1785608 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. 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 (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Feldmann, Anja Hoffmann, Anja Bergmann, Ralf Koristka, Stefanie Berndt, Nicole Arndt, Claudia Rodrigues Loureiro, Liliana Kittel-Boselli, Enrico Mitwasi, Nicola Kegler, Alexandra Lamprecht, Chris González Soto, Karla Elizabeth Bachmann, Michael Versatile chimeric antigen receptor platform for controllable and combinatorial T cell therapy |
title | Versatile chimeric antigen receptor platform for controllable and combinatorial T cell therapy |
title_full | Versatile chimeric antigen receptor platform for controllable and combinatorial T cell therapy |
title_fullStr | Versatile chimeric antigen receptor platform for controllable and combinatorial T cell therapy |
title_full_unstemmed | Versatile chimeric antigen receptor platform for controllable and combinatorial T cell therapy |
title_short | Versatile chimeric antigen receptor platform for controllable and combinatorial T cell therapy |
title_sort | versatile chimeric antigen receptor platform for controllable and combinatorial t cell therapy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458653/ https://www.ncbi.nlm.nih.gov/pubmed/32923149 http://dx.doi.org/10.1080/2162402X.2020.1785608 |
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