| Literature DB >> 26798585 |
Santiago Viteri1, María González-Cao1, Feliciano Barrón1, Aldo Riso1, Rafael Rosell1.
Abstract
One of the main hallmarks of cancer is the capability of evading immune destruction. In order to drive tumor progression, malignant cells are able to promote immunosuppressive mechanisms avoiding recognition and elimination. Increasing knowledge of the mechanisms of immune tolerance has led to the identification of several membrane receptors strongly implicated in this cancer feature: the immune checkpoints. Among them, programmed death 1 (PD-1) receptors and their ligands have been identified as potential targets for a new anti-cancer therapeutic approach: the use of immune-modulatory monoclonal antibodies designed to interrupt the immune escape activated by the interaction of PD-1 receptors and their ligands. Five of these antibodies are now in their late stages of clinical development and this review will summarize their up-to-date efficacy and toxicity data.Entities:
Keywords: Lung cancer; nivolumab; pembrolizumab; programmed death 1 (PD-1); programmed death ligand 1 (PD-L1)
Year: 2015 PMID: 26798585 PMCID: PMC4700219 DOI: 10.3978/j.issn.2218-6751.2015.12.06
Source DB: PubMed Journal: Transl Lung Cancer Res ISSN: 2218-6751