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PD1/PD-L1 immune checkpoint as a potential target for preventing brain tumor progression
Programmed death-1 (PD-1) is a cell surface receptor that functions as a T cell checkpoint and plays a central role in regulating T cell collapse. The binding of PD-1 to its ligand programmed death-ligand 1 (PD-L1) activates downstream signaling pathways and inhibits T cell activation in the perspec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374620/ https://www.ncbi.nlm.nih.gov/pubmed/35092481 http://dx.doi.org/10.1007/s00262-021-03130-z |
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author | Filippone, A. Lanza, M. Mannino, D. Raciti, G. Colarossi, C. Sciacca, D. Cuzzocrea, S. Paterniti, I. |
author_facet | Filippone, A. Lanza, M. Mannino, D. Raciti, G. Colarossi, C. Sciacca, D. Cuzzocrea, S. Paterniti, I. |
author_sort | Filippone, A. |
collection | PubMed |
description | Programmed death-1 (PD-1) is a cell surface receptor that functions as a T cell checkpoint and plays a central role in regulating T cell collapse. The binding of PD-1 to its ligand programmed death-ligand 1 (PD-L1) activates downstream signaling pathways and inhibits T cell activation in the perspective of immune system mechanism and regulation in tumor progression. It is well reported that tumors adopt certain immune-checkpoint pathways as a mechanism of resistance against immune cells such as T cells that are specific for tumor antigens. Indeed, the PD-1/PD-L1 pathway controls the induction and maintenance of immune tolerance within the tumor microenvironment. Thus, the PD-1/PD-L1 checkpoint regulation appears to be of extreme importance as well as the immunotherapy targeting that via and the using of PD-1/PD-L1 inhibitors that have changed the scenario of brain cancer treatment and survival. Here, we review the mechanism of action of PD-1 and PD-L1, the PD/PDL-1 signaling pathway involved in the progression of brain tumors, and its application as cancer immunotherapy counteracting tumor escape in central nervous system. |
format | Online Article Text |
id | pubmed-9374620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-93746202022-08-14 PD1/PD-L1 immune checkpoint as a potential target for preventing brain tumor progression Filippone, A. Lanza, M. Mannino, D. Raciti, G. Colarossi, C. Sciacca, D. Cuzzocrea, S. Paterniti, I. Cancer Immunol Immunother Review Article Programmed death-1 (PD-1) is a cell surface receptor that functions as a T cell checkpoint and plays a central role in regulating T cell collapse. The binding of PD-1 to its ligand programmed death-ligand 1 (PD-L1) activates downstream signaling pathways and inhibits T cell activation in the perspective of immune system mechanism and regulation in tumor progression. It is well reported that tumors adopt certain immune-checkpoint pathways as a mechanism of resistance against immune cells such as T cells that are specific for tumor antigens. Indeed, the PD-1/PD-L1 pathway controls the induction and maintenance of immune tolerance within the tumor microenvironment. Thus, the PD-1/PD-L1 checkpoint regulation appears to be of extreme importance as well as the immunotherapy targeting that via and the using of PD-1/PD-L1 inhibitors that have changed the scenario of brain cancer treatment and survival. Here, we review the mechanism of action of PD-1 and PD-L1, the PD/PDL-1 signaling pathway involved in the progression of brain tumors, and its application as cancer immunotherapy counteracting tumor escape in central nervous system. Springer Berlin Heidelberg 2022-01-29 2022 /pmc/articles/PMC9374620/ /pubmed/35092481 http://dx.doi.org/10.1007/s00262-021-03130-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Filippone, A. Lanza, M. Mannino, D. Raciti, G. Colarossi, C. Sciacca, D. Cuzzocrea, S. Paterniti, I. PD1/PD-L1 immune checkpoint as a potential target for preventing brain tumor progression |
title | PD1/PD-L1 immune checkpoint as a potential target for preventing brain tumor progression |
title_full | PD1/PD-L1 immune checkpoint as a potential target for preventing brain tumor progression |
title_fullStr | PD1/PD-L1 immune checkpoint as a potential target for preventing brain tumor progression |
title_full_unstemmed | PD1/PD-L1 immune checkpoint as a potential target for preventing brain tumor progression |
title_short | PD1/PD-L1 immune checkpoint as a potential target for preventing brain tumor progression |
title_sort | pd1/pd-l1 immune checkpoint as a potential target for preventing brain tumor progression |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374620/ https://www.ncbi.nlm.nih.gov/pubmed/35092481 http://dx.doi.org/10.1007/s00262-021-03130-z |
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