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CAR T-Cell Immunotherapy Treating T-ALL: Challenges and Opportunities
T-cell acute lymphoblastic leukemia (T-ALL), a form of T-cell malignancy, is a typically aggressive hematological malignancy with high rates of disease relapse and a poor prognosis. Current guidelines do not recommend any specific treatments for these patients, and only allogeneic stem cell transpla...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9861718/ https://www.ncbi.nlm.nih.gov/pubmed/36680011 http://dx.doi.org/10.3390/vaccines11010165 |
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author | Ren, Anqi Tong, Xiqin Xu, Na Zhang, Tongcun Zhou, Fuling Zhu, Haichuan |
author_facet | Ren, Anqi Tong, Xiqin Xu, Na Zhang, Tongcun Zhou, Fuling Zhu, Haichuan |
author_sort | Ren, Anqi |
collection | PubMed |
description | T-cell acute lymphoblastic leukemia (T-ALL), a form of T-cell malignancy, is a typically aggressive hematological malignancy with high rates of disease relapse and a poor prognosis. Current guidelines do not recommend any specific treatments for these patients, and only allogeneic stem cell transplant, which is associated with potential risks and toxicities, is a curative therapy. Recent clinical trials showed that immunotherapies, including monoclonal antibodies, checkpoint inhibitors, and CAR T therapies, are successful in treating hematologic malignancies. CAR T cells, which specifically target the B-cell surface antigen CD19, have demonstrated remarkable efficacy in the treatment of B-cell acute leukemia, and some progress has been made in the treatment of other hematologic malignancies. However, the development of CAR T-cell immunotherapy targeting T-cell malignancies appears more challenging due to the potential risks of fratricide, T-cell aplasia, immunosuppression, and product contamination. In this review, we discuss the current status of and challenges related to CAR T-cell immunotherapy for T-ALL and review potential strategies to overcome these limitations. |
format | Online Article Text |
id | pubmed-9861718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98617182023-01-22 CAR T-Cell Immunotherapy Treating T-ALL: Challenges and Opportunities Ren, Anqi Tong, Xiqin Xu, Na Zhang, Tongcun Zhou, Fuling Zhu, Haichuan Vaccines (Basel) Review T-cell acute lymphoblastic leukemia (T-ALL), a form of T-cell malignancy, is a typically aggressive hematological malignancy with high rates of disease relapse and a poor prognosis. Current guidelines do not recommend any specific treatments for these patients, and only allogeneic stem cell transplant, which is associated with potential risks and toxicities, is a curative therapy. Recent clinical trials showed that immunotherapies, including monoclonal antibodies, checkpoint inhibitors, and CAR T therapies, are successful in treating hematologic malignancies. CAR T cells, which specifically target the B-cell surface antigen CD19, have demonstrated remarkable efficacy in the treatment of B-cell acute leukemia, and some progress has been made in the treatment of other hematologic malignancies. However, the development of CAR T-cell immunotherapy targeting T-cell malignancies appears more challenging due to the potential risks of fratricide, T-cell aplasia, immunosuppression, and product contamination. In this review, we discuss the current status of and challenges related to CAR T-cell immunotherapy for T-ALL and review potential strategies to overcome these limitations. MDPI 2023-01-12 /pmc/articles/PMC9861718/ /pubmed/36680011 http://dx.doi.org/10.3390/vaccines11010165 Text en © 2023 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 Ren, Anqi Tong, Xiqin Xu, Na Zhang, Tongcun Zhou, Fuling Zhu, Haichuan CAR T-Cell Immunotherapy Treating T-ALL: Challenges and Opportunities |
title | CAR T-Cell Immunotherapy Treating T-ALL: Challenges and Opportunities |
title_full | CAR T-Cell Immunotherapy Treating T-ALL: Challenges and Opportunities |
title_fullStr | CAR T-Cell Immunotherapy Treating T-ALL: Challenges and Opportunities |
title_full_unstemmed | CAR T-Cell Immunotherapy Treating T-ALL: Challenges and Opportunities |
title_short | CAR T-Cell Immunotherapy Treating T-ALL: Challenges and Opportunities |
title_sort | car t-cell immunotherapy treating t-all: challenges and opportunities |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9861718/ https://www.ncbi.nlm.nih.gov/pubmed/36680011 http://dx.doi.org/10.3390/vaccines11010165 |
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