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Recent Advances in the Development of Anti-FLT3 CAR T-Cell Therapies for Treatment of AML

Following the success of the anti-CD19 chimeric antigen receptor (CAR) T-cell therapies against B-cell malignancies, the CAR T-cell approach is being developed towards other malignancies like acute myeloid leukemia (AML). Treatment options for relapsed AML patients are limited, and the upregulation...

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Autores principales: Pedersen, Maya Graham, Møller, Bjarne Kuno, Bak, Rasmus O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598885/
https://www.ncbi.nlm.nih.gov/pubmed/36289703
http://dx.doi.org/10.3390/biomedicines10102441
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author Pedersen, Maya Graham
Møller, Bjarne Kuno
Bak, Rasmus O.
author_facet Pedersen, Maya Graham
Møller, Bjarne Kuno
Bak, Rasmus O.
author_sort Pedersen, Maya Graham
collection PubMed
description Following the success of the anti-CD19 chimeric antigen receptor (CAR) T-cell therapies against B-cell malignancies, the CAR T-cell approach is being developed towards other malignancies like acute myeloid leukemia (AML). Treatment options for relapsed AML patients are limited, and the upregulation of the FMS-like tyrosine kinase 3 (FLT3) in malignant T-cells is currently not only being investigated as a prognostic factor, but also as a target for new treatment options. In this review, we provide an overview and discuss different approaches of current anti-FLT3 CAR T-cells under development. In general, these therapies are effective both in vitro and in vivo, however the safety profile still needs to be further investigated. The first clinical trials have been initiated, and the community now awaits clinical evaluation of the approach of targeting FLT3 with CAR T-cells.
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spelling pubmed-95988852022-10-27 Recent Advances in the Development of Anti-FLT3 CAR T-Cell Therapies for Treatment of AML Pedersen, Maya Graham Møller, Bjarne Kuno Bak, Rasmus O. Biomedicines Review Following the success of the anti-CD19 chimeric antigen receptor (CAR) T-cell therapies against B-cell malignancies, the CAR T-cell approach is being developed towards other malignancies like acute myeloid leukemia (AML). Treatment options for relapsed AML patients are limited, and the upregulation of the FMS-like tyrosine kinase 3 (FLT3) in malignant T-cells is currently not only being investigated as a prognostic factor, but also as a target for new treatment options. In this review, we provide an overview and discuss different approaches of current anti-FLT3 CAR T-cells under development. In general, these therapies are effective both in vitro and in vivo, however the safety profile still needs to be further investigated. The first clinical trials have been initiated, and the community now awaits clinical evaluation of the approach of targeting FLT3 with CAR T-cells. MDPI 2022-09-30 /pmc/articles/PMC9598885/ /pubmed/36289703 http://dx.doi.org/10.3390/biomedicines10102441 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pedersen, Maya Graham
Møller, Bjarne Kuno
Bak, Rasmus O.
Recent Advances in the Development of Anti-FLT3 CAR T-Cell Therapies for Treatment of AML
title Recent Advances in the Development of Anti-FLT3 CAR T-Cell Therapies for Treatment of AML
title_full Recent Advances in the Development of Anti-FLT3 CAR T-Cell Therapies for Treatment of AML
title_fullStr Recent Advances in the Development of Anti-FLT3 CAR T-Cell Therapies for Treatment of AML
title_full_unstemmed Recent Advances in the Development of Anti-FLT3 CAR T-Cell Therapies for Treatment of AML
title_short Recent Advances in the Development of Anti-FLT3 CAR T-Cell Therapies for Treatment of AML
title_sort recent advances in the development of anti-flt3 car t-cell therapies for treatment of aml
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598885/
https://www.ncbi.nlm.nih.gov/pubmed/36289703
http://dx.doi.org/10.3390/biomedicines10102441
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