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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Association of Immunologists
2022
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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. |
format | Online Article Text |
id | pubmed-8901698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Korean Association of Immunologists |
record_format | MEDLINE/PubMed |
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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