Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mirzaei, Hamid R., Rodriguez, Analiz, Shepphird, Jennifer, Brown, Christine E., Badie, Behnam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
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
_version_ 1783288670815518720
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
work_keys_str_mv AT mirzaeihamidr chimericantigenreceptorstcelltherapyinsolidtumorchallengesandclinicalapplications
AT rodriguezanaliz chimericantigenreceptorstcelltherapyinsolidtumorchallengesandclinicalapplications
AT shepphirdjennifer chimericantigenreceptorstcelltherapyinsolidtumorchallengesandclinicalapplications
AT brownchristinee chimericantigenreceptorstcelltherapyinsolidtumorchallengesandclinicalapplications
AT badiebehnam chimericantigenreceptorstcelltherapyinsolidtumorchallengesandclinicalapplications