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Multi Targeted CAR-T Cell Therapies for B-Cell Malignancies
Chimeric antigen receptor (CAR) modified T cell therapy has revolutionized the treatment of relapsed and refractory hematological malignancies. Through targeting of the CD19 antigen on B cells durable remissions have been achieved in patients with B cell non-Hodgkin lymphoma and acute lymphoblastic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423158/ https://www.ncbi.nlm.nih.gov/pubmed/30915277 http://dx.doi.org/10.3389/fonc.2019.00146 |
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author | Shah, Nirav N. Maatman, Theresa Hari, Parameswaran Johnson, Bryon |
author_facet | Shah, Nirav N. Maatman, Theresa Hari, Parameswaran Johnson, Bryon |
author_sort | Shah, Nirav N. |
collection | PubMed |
description | Chimeric antigen receptor (CAR) modified T cell therapy has revolutionized the treatment of relapsed and refractory hematological malignancies. Through targeting of the CD19 antigen on B cells durable remissions have been achieved in patients with B cell non-Hodgkin lymphoma and acute lymphoblastic lymphoma. Despite impressive responses, multiple escape mechanisms to evade CAR-T cell therapy have been identified, among which the most common is loss of the target antigen. In this review we will highlight outcomes to date with CD19 CAR-T cell therapy, describe the current limitations of single targeted CAR-T therapies, review identified tumor escape mechanisms, and lastly discuss novel strategies to overcome resistance via multi-targeted CAR-T cells. |
format | Online Article Text |
id | pubmed-6423158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64231582019-03-26 Multi Targeted CAR-T Cell Therapies for B-Cell Malignancies Shah, Nirav N. Maatman, Theresa Hari, Parameswaran Johnson, Bryon Front Oncol Oncology Chimeric antigen receptor (CAR) modified T cell therapy has revolutionized the treatment of relapsed and refractory hematological malignancies. Through targeting of the CD19 antigen on B cells durable remissions have been achieved in patients with B cell non-Hodgkin lymphoma and acute lymphoblastic lymphoma. Despite impressive responses, multiple escape mechanisms to evade CAR-T cell therapy have been identified, among which the most common is loss of the target antigen. In this review we will highlight outcomes to date with CD19 CAR-T cell therapy, describe the current limitations of single targeted CAR-T therapies, review identified tumor escape mechanisms, and lastly discuss novel strategies to overcome resistance via multi-targeted CAR-T cells. Frontiers Media S.A. 2019-03-12 /pmc/articles/PMC6423158/ /pubmed/30915277 http://dx.doi.org/10.3389/fonc.2019.00146 Text en Copyright © 2019 Shah, Maatman, Hari and Johnson. 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 Shah, Nirav N. Maatman, Theresa Hari, Parameswaran Johnson, Bryon Multi Targeted CAR-T Cell Therapies for B-Cell Malignancies |
title | Multi Targeted CAR-T Cell Therapies for B-Cell Malignancies |
title_full | Multi Targeted CAR-T Cell Therapies for B-Cell Malignancies |
title_fullStr | Multi Targeted CAR-T Cell Therapies for B-Cell Malignancies |
title_full_unstemmed | Multi Targeted CAR-T Cell Therapies for B-Cell Malignancies |
title_short | Multi Targeted CAR-T Cell Therapies for B-Cell Malignancies |
title_sort | multi targeted car-t cell therapies for b-cell malignancies |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423158/ https://www.ncbi.nlm.nih.gov/pubmed/30915277 http://dx.doi.org/10.3389/fonc.2019.00146 |
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