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Improving CAR-T immunotherapy: Overcoming the challenges of T cell exhaustion
Chimeric antigen receptor (CAR) T cell therapy has emerged as a cancer treatment with enormous potential, demonstrating impressive antitumor activity in the treatment of hematological malignancies. However, CAR T cell exhaustion is a major limitation to their efficacy, particularly in the applicatio...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927848/ https://www.ncbi.nlm.nih.gov/pubmed/35301179 http://dx.doi.org/10.1016/j.ebiom.2022.103941 |
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author | Gumber, Diana Wang, Leo D. |
author_facet | Gumber, Diana Wang, Leo D. |
author_sort | Gumber, Diana |
collection | PubMed |
description | Chimeric antigen receptor (CAR) T cell therapy has emerged as a cancer treatment with enormous potential, demonstrating impressive antitumor activity in the treatment of hematological malignancies. However, CAR T cell exhaustion is a major limitation to their efficacy, particularly in the application of CAR T cells to solid tumors. CAR T cell exhaustion is thought to be due to persistent antigen stimulation, as well as an immunosuppressive tumor microenvironment, and mitigating exhaustion to maintain CAR T cell effector function and persistence and achieve clinical potency remains a central challenge. Here, we review the underlying mechanisms of exhaustion and discuss emerging strategies to prevent or reverse exhaustion through modifications of the CAR receptor or CAR independent pathways. Additionally, we discuss the potential of these strategies for improving clinical outcomes of CAR T cell therapy. |
format | Online Article Text |
id | pubmed-8927848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-89278482022-03-18 Improving CAR-T immunotherapy: Overcoming the challenges of T cell exhaustion Gumber, Diana Wang, Leo D. EBioMedicine Review Chimeric antigen receptor (CAR) T cell therapy has emerged as a cancer treatment with enormous potential, demonstrating impressive antitumor activity in the treatment of hematological malignancies. However, CAR T cell exhaustion is a major limitation to their efficacy, particularly in the application of CAR T cells to solid tumors. CAR T cell exhaustion is thought to be due to persistent antigen stimulation, as well as an immunosuppressive tumor microenvironment, and mitigating exhaustion to maintain CAR T cell effector function and persistence and achieve clinical potency remains a central challenge. Here, we review the underlying mechanisms of exhaustion and discuss emerging strategies to prevent or reverse exhaustion through modifications of the CAR receptor or CAR independent pathways. Additionally, we discuss the potential of these strategies for improving clinical outcomes of CAR T cell therapy. Elsevier 2022-03-15 /pmc/articles/PMC8927848/ /pubmed/35301179 http://dx.doi.org/10.1016/j.ebiom.2022.103941 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Gumber, Diana Wang, Leo D. Improving CAR-T immunotherapy: Overcoming the challenges of T cell exhaustion |
title | Improving CAR-T immunotherapy: Overcoming the challenges of T cell exhaustion |
title_full | Improving CAR-T immunotherapy: Overcoming the challenges of T cell exhaustion |
title_fullStr | Improving CAR-T immunotherapy: Overcoming the challenges of T cell exhaustion |
title_full_unstemmed | Improving CAR-T immunotherapy: Overcoming the challenges of T cell exhaustion |
title_short | Improving CAR-T immunotherapy: Overcoming the challenges of T cell exhaustion |
title_sort | improving car-t immunotherapy: overcoming the challenges of t cell exhaustion |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927848/ https://www.ncbi.nlm.nih.gov/pubmed/35301179 http://dx.doi.org/10.1016/j.ebiom.2022.103941 |
work_keys_str_mv | AT gumberdiana improvingcartimmunotherapyovercomingthechallengesoftcellexhaustion AT wangleod improvingcartimmunotherapyovercomingthechallengesoftcellexhaustion |