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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...

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Detalles Bibliográficos
Autores principales: Zitvogel, Laurence, Kroemer, Guido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
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.
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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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