背景(考古学)
医学
免疫疗法
PD-L1
免疫检查点
癌症
内科学
生物
古生物学
作者
Claire Vanpouille‐Box,Claire Lhuillier,Lucillia Bezu,Fernando Aranda,Takahiro Yamazaki,Oliver Kepp,Jitka Fučíková,Radek Špíšek,Sandra Demaria,Silvia C. Formenti,Laurence Zitvogel,Guido Kroemer,Lorenzo Galluzzi
出处
期刊:OncoImmunology
[Informa]
日期:2017-08-31
卷期号:6 (11): e1373237-e1373237
被引量:68
标识
DOI:10.1080/2162402x.2017.1373237
摘要
Immune checkpoint blockers (ICBs) are literally revolutionizing the clinical management of an ever more diversified panel of oncological indications. Although considerable attention persists around the inhibition of cytotoxic T lymphocyte-associated protein 4 (CTLA4) and programmed cell death 1 (PDCD1, best known as PD-1) signaling, several other co-inhibitory T-cell receptors are being evaluated as potential targets for the development of novel ICBs. Moreover, substantial efforts are being devoted to the identification of biomarkers that reliably predict the likelihood of each patient to obtain clinical benefits from ICBs in the absence of severe toxicity. Tailoring the delivery of specific ICBs or combinations thereof to selected patient populations in the context of precision medicine programs constitutes indeed a major objective of the future of ICB-based immunotherapy. Here, we discuss recent preclinical and clinical advances on the development of ICBs for oncological indications.
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