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Programmed Death Ligand 2 in Cancer-Induced Immune Suppression
Inhibitory molecules of the B7/CD28 family play a key role in the induction of immune tolerance in the tumor microenvironment. The programmed death-1 receptor (PD-1), with its ligands PD-L1 and PD-L2, constitutes an important member of these inhibitory pathways. The relevance of the PD-1/PD-L1 pathw...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350956/ https://www.ncbi.nlm.nih.gov/pubmed/22611421 http://dx.doi.org/10.1155/2012/656340 |
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author | Rozali, Esdy N. Hato, Stanleyson V. Robinson, Bruce W. Lake, Richard A. Lesterhuis, W. Joost |
author_facet | Rozali, Esdy N. Hato, Stanleyson V. Robinson, Bruce W. Lake, Richard A. Lesterhuis, W. Joost |
author_sort | Rozali, Esdy N. |
collection | PubMed |
description | Inhibitory molecules of the B7/CD28 family play a key role in the induction of immune tolerance in the tumor microenvironment. The programmed death-1 receptor (PD-1), with its ligands PD-L1 and PD-L2, constitutes an important member of these inhibitory pathways. The relevance of the PD-1/PD-L1 pathway in cancer has been extensively studied and therapeutic approaches targeting PD-1 and PD-L1 have been developed and are undergoing human clinical testing. However, PD-L2 has not received as much attention and its role in modulating tumor immunity is less clear. Here, we review the literature on the immunobiology of PD-L2, particularly on its possible roles in cancer-induced immune suppression and we discuss the results of recent studies targeting PD-L2 in cancer. |
format | Online Article Text |
id | pubmed-3350956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33509562012-05-18 Programmed Death Ligand 2 in Cancer-Induced Immune Suppression Rozali, Esdy N. Hato, Stanleyson V. Robinson, Bruce W. Lake, Richard A. Lesterhuis, W. Joost Clin Dev Immunol Review Article Inhibitory molecules of the B7/CD28 family play a key role in the induction of immune tolerance in the tumor microenvironment. The programmed death-1 receptor (PD-1), with its ligands PD-L1 and PD-L2, constitutes an important member of these inhibitory pathways. The relevance of the PD-1/PD-L1 pathway in cancer has been extensively studied and therapeutic approaches targeting PD-1 and PD-L1 have been developed and are undergoing human clinical testing. However, PD-L2 has not received as much attention and its role in modulating tumor immunity is less clear. Here, we review the literature on the immunobiology of PD-L2, particularly on its possible roles in cancer-induced immune suppression and we discuss the results of recent studies targeting PD-L2 in cancer. Hindawi Publishing Corporation 2012 2012-04-29 /pmc/articles/PMC3350956/ /pubmed/22611421 http://dx.doi.org/10.1155/2012/656340 Text en Copyright © 2012 Esdy N. Rozali et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Rozali, Esdy N. Hato, Stanleyson V. Robinson, Bruce W. Lake, Richard A. Lesterhuis, W. Joost Programmed Death Ligand 2 in Cancer-Induced Immune Suppression |
title | Programmed Death Ligand 2 in Cancer-Induced Immune Suppression |
title_full | Programmed Death Ligand 2 in Cancer-Induced Immune Suppression |
title_fullStr | Programmed Death Ligand 2 in Cancer-Induced Immune Suppression |
title_full_unstemmed | Programmed Death Ligand 2 in Cancer-Induced Immune Suppression |
title_short | Programmed Death Ligand 2 in Cancer-Induced Immune Suppression |
title_sort | programmed death ligand 2 in cancer-induced immune suppression |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350956/ https://www.ncbi.nlm.nih.gov/pubmed/22611421 http://dx.doi.org/10.1155/2012/656340 |
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