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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
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.
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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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