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Targeting PD-1/PD-L1 interactions for cancer immunotherapy
Tumors have developed multiple immunosuppressive mechanisms to turn down the innate and the effector arms of the immune system, thus compromising most of the immunotherapeutic strategies that have been proposed during the last decade. Right after the pioneering success of Ipilimumab (anti-CTLA4) in...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518493/ https://www.ncbi.nlm.nih.gov/pubmed/23243584 http://dx.doi.org/10.4161/onci.21335 |
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author | Zitvogel, Laurence Kroemer, Guido |
author_facet | Zitvogel, Laurence Kroemer, Guido |
author_sort | Zitvogel, Laurence |
collection | PubMed |
description | Tumors have developed multiple immunosuppressive mechanisms to turn down the innate and the effector arms of the immune system, thus compromising most of the immunotherapeutic strategies that have been proposed during the last decade. Right after the pioneering success of Ipilimumab (anti-CTLA4) in metastatic melanoma, several groups have conducted trials aiming at subverting other immune checkpoints. Two articles that recently appeared in the New England Journal of Medicine.(1)(,)(2) highlight the therapeutic potential of agents that target PD-1 or its ligand PD-L1 in patients with advanced cancer, even individuals with lung or brain metastases. If confirmed, this clinical breakthrough will open novel avenues for cancer immunotherapy. |
format | Online Article Text |
id | pubmed-3518493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-35184932012-12-14 Targeting PD-1/PD-L1 interactions for cancer immunotherapy Zitvogel, Laurence Kroemer, Guido Oncoimmunology Editor's Corner Tumors have developed multiple immunosuppressive mechanisms to turn down the innate and the effector arms of the immune system, thus compromising most of the immunotherapeutic strategies that have been proposed during the last decade. Right after the pioneering success of Ipilimumab (anti-CTLA4) in metastatic melanoma, several groups have conducted trials aiming at subverting other immune checkpoints. Two articles that recently appeared in the New England Journal of Medicine.(1)(,)(2) highlight the therapeutic potential of agents that target PD-1 or its ligand PD-L1 in patients with advanced cancer, even individuals with lung or brain metastases. If confirmed, this clinical breakthrough will open novel avenues for cancer immunotherapy. Landes Bioscience 2012-11-01 /pmc/articles/PMC3518493/ /pubmed/23243584 http://dx.doi.org/10.4161/onci.21335 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Editor's Corner Zitvogel, Laurence Kroemer, Guido Targeting PD-1/PD-L1 interactions for cancer immunotherapy |
title | Targeting PD-1/PD-L1 interactions for cancer immunotherapy |
title_full | Targeting PD-1/PD-L1 interactions for cancer immunotherapy |
title_fullStr | Targeting PD-1/PD-L1 interactions for cancer immunotherapy |
title_full_unstemmed | Targeting PD-1/PD-L1 interactions for cancer immunotherapy |
title_short | Targeting PD-1/PD-L1 interactions for cancer immunotherapy |
title_sort | targeting pd-1/pd-l1 interactions for cancer immunotherapy |
topic | Editor's Corner |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518493/ https://www.ncbi.nlm.nih.gov/pubmed/23243584 http://dx.doi.org/10.4161/onci.21335 |
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