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Racing CARs to veterinary immuno-oncology

Chimeric antigen receptors (CARs) have demonstrated remarkable promise in human oncology over the past two decades, yet similar strategies in veterinary medicine are still in development. CARs are synthetically engineered proteins comprised of a specific antigen-binding single chain variable fragmen...

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Detalles Bibliográficos
Autores principales: Cockey, James R., Leifer, Cynthia A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982037/
https://www.ncbi.nlm.nih.gov/pubmed/36876006
http://dx.doi.org/10.3389/fvets.2023.1130182
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author Cockey, James R.
Leifer, Cynthia A.
author_facet Cockey, James R.
Leifer, Cynthia A.
author_sort Cockey, James R.
collection PubMed
description Chimeric antigen receptors (CARs) have demonstrated remarkable promise in human oncology over the past two decades, yet similar strategies in veterinary medicine are still in development. CARs are synthetically engineered proteins comprised of a specific antigen-binding single chain variable fragment (ScFv) fused to the signaling domain of a T cell receptor and co-receptors. Patient T cells engineered to express a CAR are directed to recognize and kill target cells, most commonly hematological malignancies. The U.S Food and Drug Administration (FDA) has approved multiple human CAR T therapies, but translation of these therapies into veterinary medicine faces many challenges. In this review, we discuss considerations for veterinary use including CAR design and cell carrier choice, and discuss the future promise of translating CAR therapy into veterinary oncology.
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spelling pubmed-99820372023-03-04 Racing CARs to veterinary immuno-oncology Cockey, James R. Leifer, Cynthia A. Front Vet Sci Veterinary Science Chimeric antigen receptors (CARs) have demonstrated remarkable promise in human oncology over the past two decades, yet similar strategies in veterinary medicine are still in development. CARs are synthetically engineered proteins comprised of a specific antigen-binding single chain variable fragment (ScFv) fused to the signaling domain of a T cell receptor and co-receptors. Patient T cells engineered to express a CAR are directed to recognize and kill target cells, most commonly hematological malignancies. The U.S Food and Drug Administration (FDA) has approved multiple human CAR T therapies, but translation of these therapies into veterinary medicine faces many challenges. In this review, we discuss considerations for veterinary use including CAR design and cell carrier choice, and discuss the future promise of translating CAR therapy into veterinary oncology. Frontiers Media S.A. 2023-02-17 /pmc/articles/PMC9982037/ /pubmed/36876006 http://dx.doi.org/10.3389/fvets.2023.1130182 Text en Copyright © 2023 Cockey and Leifer. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Veterinary Science
Cockey, James R.
Leifer, Cynthia A.
Racing CARs to veterinary immuno-oncology
title Racing CARs to veterinary immuno-oncology
title_full Racing CARs to veterinary immuno-oncology
title_fullStr Racing CARs to veterinary immuno-oncology
title_full_unstemmed Racing CARs to veterinary immuno-oncology
title_short Racing CARs to veterinary immuno-oncology
title_sort racing cars to veterinary immuno-oncology
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982037/
https://www.ncbi.nlm.nih.gov/pubmed/36876006
http://dx.doi.org/10.3389/fvets.2023.1130182
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