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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...

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Autores principales: Shah, Nirav N., Maatman, Theresa, Hari, Parameswaran, Johnson, Bryon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
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.
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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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