Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Gumber, Diana, Wang, Leo D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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
_version_ 1784670535707262976
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