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CAR T Cell Immunotherapy Beyond Haematological Malignancy

Chimeric antigen receptor (CAR) T cells, which express a synthetic receptor engineered to target specific antigens, have demonstrated remarkable potential to treat haematological malignancies. However, their transition beyond haematological malignancy has so far been unsatisfactory. Here, we discuss...

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Detalles Bibliográficos
Autores principales: Hupperetz, Cedric, Lah, Sangjoon, Kim, Hyojin, Kim, Chan Hyuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901698/
https://www.ncbi.nlm.nih.gov/pubmed/35291659
http://dx.doi.org/10.4110/in.2022.22.e6
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author Hupperetz, Cedric
Lah, Sangjoon
Kim, Hyojin
Kim, Chan Hyuk
author_facet Hupperetz, Cedric
Lah, Sangjoon
Kim, Hyojin
Kim, Chan Hyuk
author_sort Hupperetz, Cedric
collection PubMed
description Chimeric antigen receptor (CAR) T cells, which express a synthetic receptor engineered to target specific antigens, have demonstrated remarkable potential to treat haematological malignancies. However, their transition beyond haematological malignancy has so far been unsatisfactory. Here, we discuss recent challenges and improvements for CAR T cell therapy against solid tumors: Antigen heterogeneity which provides an effective escape mechanism against conventional mono-antigen-specific CAR T cells; and the immunosuppressive tumor microenvironment which provides physical and molecular barriers that respectively prevent T cell infiltration and drive T cell dysfunction and hypoproliferation. Further, we discuss the application of CAR T cells in infectious disease and autoimmunity.
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spelling pubmed-89016982022-03-14 CAR T Cell Immunotherapy Beyond Haematological Malignancy Hupperetz, Cedric Lah, Sangjoon Kim, Hyojin Kim, Chan Hyuk Immune Netw Review Article Chimeric antigen receptor (CAR) T cells, which express a synthetic receptor engineered to target specific antigens, have demonstrated remarkable potential to treat haematological malignancies. However, their transition beyond haematological malignancy has so far been unsatisfactory. Here, we discuss recent challenges and improvements for CAR T cell therapy against solid tumors: Antigen heterogeneity which provides an effective escape mechanism against conventional mono-antigen-specific CAR T cells; and the immunosuppressive tumor microenvironment which provides physical and molecular barriers that respectively prevent T cell infiltration and drive T cell dysfunction and hypoproliferation. Further, we discuss the application of CAR T cells in infectious disease and autoimmunity. The Korean Association of Immunologists 2022-02-11 /pmc/articles/PMC8901698/ /pubmed/35291659 http://dx.doi.org/10.4110/in.2022.22.e6 Text en Copyright © 2022. The Korean Association of Immunologists https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Hupperetz, Cedric
Lah, Sangjoon
Kim, Hyojin
Kim, Chan Hyuk
CAR T Cell Immunotherapy Beyond Haematological Malignancy
title CAR T Cell Immunotherapy Beyond Haematological Malignancy
title_full CAR T Cell Immunotherapy Beyond Haematological Malignancy
title_fullStr CAR T Cell Immunotherapy Beyond Haematological Malignancy
title_full_unstemmed CAR T Cell Immunotherapy Beyond Haematological Malignancy
title_short CAR T Cell Immunotherapy Beyond Haematological Malignancy
title_sort car t cell immunotherapy beyond haematological malignancy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901698/
https://www.ncbi.nlm.nih.gov/pubmed/35291659
http://dx.doi.org/10.4110/in.2022.22.e6
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