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Current Advances in CAR T Cell Therapy for Malignant Mesothelioma

Malignant mesothelioma is a relatively rare malignancy arising in the body’s serosal surfaces, with malignant pleural mesothelioma (MPM) being the most common type. It is characterized by local spread within the thorax, poor prognosis and resistance to treatment. The development of various immunothe...

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Autores principales: Klampatsa, Astero, Albelda, Steven M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480947/
https://www.ncbi.nlm.nih.gov/pubmed/32914147
http://dx.doi.org/10.33696/immunology.2.042
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author Klampatsa, Astero
Albelda, Steven M.
author_facet Klampatsa, Astero
Albelda, Steven M.
author_sort Klampatsa, Astero
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description Malignant mesothelioma is a relatively rare malignancy arising in the body’s serosal surfaces, with malignant pleural mesothelioma (MPM) being the most common type. It is characterized by local spread within the thorax, poor prognosis and resistance to treatment. The development of various immunotherapeutic options has provided a new way- and hope- in treating cancer patients. Chimeric antigen receptor (CAR) T cell therapy has been proven very successful in treating hematological cancers, like leukemias and lymphomas, and its use is now being tested in solid tumors. CARs that recognize and bind to a specific tumor-associated antigen on the tumor’s cell surface, are engineered and transduced into T cells. Interaction of the CAR T cell with the tumor then results in T cell activation and subsequent tumor cell lysis. In this review, we provide a current update on our previous comprehensive study summarizing the CAR T cell preclinical studies and clinical trials in MM, and discuss the future perspectives of CAR T cell therapy in this disease.
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spelling pubmed-74809472020-09-09 Current Advances in CAR T Cell Therapy for Malignant Mesothelioma Klampatsa, Astero Albelda, Steven M. J Cell Immunol Article Malignant mesothelioma is a relatively rare malignancy arising in the body’s serosal surfaces, with malignant pleural mesothelioma (MPM) being the most common type. It is characterized by local spread within the thorax, poor prognosis and resistance to treatment. The development of various immunotherapeutic options has provided a new way- and hope- in treating cancer patients. Chimeric antigen receptor (CAR) T cell therapy has been proven very successful in treating hematological cancers, like leukemias and lymphomas, and its use is now being tested in solid tumors. CARs that recognize and bind to a specific tumor-associated antigen on the tumor’s cell surface, are engineered and transduced into T cells. Interaction of the CAR T cell with the tumor then results in T cell activation and subsequent tumor cell lysis. In this review, we provide a current update on our previous comprehensive study summarizing the CAR T cell preclinical studies and clinical trials in MM, and discuss the future perspectives of CAR T cell therapy in this disease. 2020 /pmc/articles/PMC7480947/ /pubmed/32914147 http://dx.doi.org/10.33696/immunology.2.042 Text en This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Klampatsa, Astero
Albelda, Steven M.
Current Advances in CAR T Cell Therapy for Malignant Mesothelioma
title Current Advances in CAR T Cell Therapy for Malignant Mesothelioma
title_full Current Advances in CAR T Cell Therapy for Malignant Mesothelioma
title_fullStr Current Advances in CAR T Cell Therapy for Malignant Mesothelioma
title_full_unstemmed Current Advances in CAR T Cell Therapy for Malignant Mesothelioma
title_short Current Advances in CAR T Cell Therapy for Malignant Mesothelioma
title_sort current advances in car t cell therapy for malignant mesothelioma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480947/
https://www.ncbi.nlm.nih.gov/pubmed/32914147
http://dx.doi.org/10.33696/immunology.2.042
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