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Chimeric Antigen Receptors T Cell Therapy in Solid Tumor: Challenges and Clinical Applications
Adoptive cellular immunotherapy (ACT) employing engineered T lymphocytes expressing chimeric antigen receptors (CARs) has demonstrated promising antitumor effects in advanced hematologic cancers, such as relapsed or refractory acute lymphoblastic leukemia, chronic lymphocytic leukemia, and non-Hodgk...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744011/ https://www.ncbi.nlm.nih.gov/pubmed/29312333 http://dx.doi.org/10.3389/fimmu.2017.01850 |
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author | Mirzaei, Hamid R. Rodriguez, Analiz Shepphird, Jennifer Brown, Christine E. Badie, Behnam |
author_facet | Mirzaei, Hamid R. Rodriguez, Analiz Shepphird, Jennifer Brown, Christine E. Badie, Behnam |
author_sort | Mirzaei, Hamid R. |
collection | PubMed |
description | Adoptive cellular immunotherapy (ACT) employing engineered T lymphocytes expressing chimeric antigen receptors (CARs) has demonstrated promising antitumor effects in advanced hematologic cancers, such as relapsed or refractory acute lymphoblastic leukemia, chronic lymphocytic leukemia, and non-Hodgkin lymphoma, supporting the translation of ACT to non-hematological malignancies. Although CAR T cell therapy has made remarkable strides in the treatment of patients with certain hematological cancers, in solid tumors success has been limited likely due to heterogeneous antigen expression, immunosuppressive networks in the tumor microenvironment limiting CAR T cell function and persistence, and suboptimal trafficking to solid tumors. Here, we outline specific approaches to overcome barriers to CAR T cell effectiveness in the context of the tumor microenvironment and offer our perspective on how expanding the use of CAR T cells in solid tumors may require modifications in CAR T cell design. We anticipate these modifications will further expand CAR T cell therapy in clinical practice. |
format | Online Article Text |
id | pubmed-5744011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57440112018-01-08 Chimeric Antigen Receptors T Cell Therapy in Solid Tumor: Challenges and Clinical Applications Mirzaei, Hamid R. Rodriguez, Analiz Shepphird, Jennifer Brown, Christine E. Badie, Behnam Front Immunol Immunology Adoptive cellular immunotherapy (ACT) employing engineered T lymphocytes expressing chimeric antigen receptors (CARs) has demonstrated promising antitumor effects in advanced hematologic cancers, such as relapsed or refractory acute lymphoblastic leukemia, chronic lymphocytic leukemia, and non-Hodgkin lymphoma, supporting the translation of ACT to non-hematological malignancies. Although CAR T cell therapy has made remarkable strides in the treatment of patients with certain hematological cancers, in solid tumors success has been limited likely due to heterogeneous antigen expression, immunosuppressive networks in the tumor microenvironment limiting CAR T cell function and persistence, and suboptimal trafficking to solid tumors. Here, we outline specific approaches to overcome barriers to CAR T cell effectiveness in the context of the tumor microenvironment and offer our perspective on how expanding the use of CAR T cells in solid tumors may require modifications in CAR T cell design. We anticipate these modifications will further expand CAR T cell therapy in clinical practice. Frontiers Media S.A. 2017-12-22 /pmc/articles/PMC5744011/ /pubmed/29312333 http://dx.doi.org/10.3389/fimmu.2017.01850 Text en Copyright © 2017 Mirzaei, Rodriguez, Shepphird, Brown and Badie. 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) or licensor 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 | Immunology Mirzaei, Hamid R. Rodriguez, Analiz Shepphird, Jennifer Brown, Christine E. Badie, Behnam Chimeric Antigen Receptors T Cell Therapy in Solid Tumor: Challenges and Clinical Applications |
title | Chimeric Antigen Receptors T Cell Therapy in Solid Tumor: Challenges and Clinical Applications |
title_full | Chimeric Antigen Receptors T Cell Therapy in Solid Tumor: Challenges and Clinical Applications |
title_fullStr | Chimeric Antigen Receptors T Cell Therapy in Solid Tumor: Challenges and Clinical Applications |
title_full_unstemmed | Chimeric Antigen Receptors T Cell Therapy in Solid Tumor: Challenges and Clinical Applications |
title_short | Chimeric Antigen Receptors T Cell Therapy in Solid Tumor: Challenges and Clinical Applications |
title_sort | chimeric antigen receptors t cell therapy in solid tumor: challenges and clinical applications |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744011/ https://www.ncbi.nlm.nih.gov/pubmed/29312333 http://dx.doi.org/10.3389/fimmu.2017.01850 |
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