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CAR-Based Approaches to Cutaneous T-Cell Lymphoma

Cutaneous T cell lymphomas (CTCL) are a heterogeneous group of malignancies characterized by the expansion of a malignant T cell clone. Chimeric Antigen Receptor (CAR) T cell therapy has shown impressive results for the treatment of B-cell tumors, but several challenges have prevented this approach...

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Detalles Bibliográficos
Autores principales: Scarfò, Irene, Frigault, Matthew J., Maus, Marcela V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477509/
https://www.ncbi.nlm.nih.gov/pubmed/31058076
http://dx.doi.org/10.3389/fonc.2019.00259
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author Scarfò, Irene
Frigault, Matthew J.
Maus, Marcela V.
author_facet Scarfò, Irene
Frigault, Matthew J.
Maus, Marcela V.
author_sort Scarfò, Irene
collection PubMed
description Cutaneous T cell lymphomas (CTCL) are a heterogeneous group of malignancies characterized by the expansion of a malignant T cell clone. Chimeric Antigen Receptor (CAR) T cell therapy has shown impressive results for the treatment of B-cell tumors, but several challenges have prevented this approach in the context of T cell lymphoma. These challenges include the possibilities of fratricide due to shared T-cell antigens, T cell immunodeficiency, and CAR transduction of malignant cells if CAR T are manufactured in the autologous setting. In this review, we discuss these and other challenges in detail and summarize the approaches currently in development to overcome these challenges and offer cellular targeting of T cell lymphomas.
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spelling pubmed-64775092019-05-03 CAR-Based Approaches to Cutaneous T-Cell Lymphoma Scarfò, Irene Frigault, Matthew J. Maus, Marcela V. Front Oncol Oncology Cutaneous T cell lymphomas (CTCL) are a heterogeneous group of malignancies characterized by the expansion of a malignant T cell clone. Chimeric Antigen Receptor (CAR) T cell therapy has shown impressive results for the treatment of B-cell tumors, but several challenges have prevented this approach in the context of T cell lymphoma. These challenges include the possibilities of fratricide due to shared T-cell antigens, T cell immunodeficiency, and CAR transduction of malignant cells if CAR T are manufactured in the autologous setting. In this review, we discuss these and other challenges in detail and summarize the approaches currently in development to overcome these challenges and offer cellular targeting of T cell lymphomas. Frontiers Media S.A. 2019-04-16 /pmc/articles/PMC6477509/ /pubmed/31058076 http://dx.doi.org/10.3389/fonc.2019.00259 Text en Copyright © 2019 Scarfò, Frigault and Maus. http://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 Oncology
Scarfò, Irene
Frigault, Matthew J.
Maus, Marcela V.
CAR-Based Approaches to Cutaneous T-Cell Lymphoma
title CAR-Based Approaches to Cutaneous T-Cell Lymphoma
title_full CAR-Based Approaches to Cutaneous T-Cell Lymphoma
title_fullStr CAR-Based Approaches to Cutaneous T-Cell Lymphoma
title_full_unstemmed CAR-Based Approaches to Cutaneous T-Cell Lymphoma
title_short CAR-Based Approaches to Cutaneous T-Cell Lymphoma
title_sort car-based approaches to cutaneous t-cell lymphoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477509/
https://www.ncbi.nlm.nih.gov/pubmed/31058076
http://dx.doi.org/10.3389/fonc.2019.00259
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