干扰素
生物
信号转导
免疫系统
细胞生物学
PD-L1
受体
免疫疗法
化学
免疫学
生物化学
作者
Ángel García-Díaz,Daniel Sanghoon Shin,Blanca Homet Moreno,Justin D. Saco,Helena Escuin-Ordinas,Gabriel Abril Rodriguez,Jesse M. Zaretsky,Lu Sun,Willy Hugo,Xiaoyan Wang,Giulia Parisi,Cristina Puig-Saus,Davis Y. Torrejon,Thomas G. Graeber,Begonya Comin-Anduix,Siwen Hu‐Lieskovan,Robert Damoiseaux,Roger S. Lo,Antoni Ribas
出处
期刊:Cell Reports
[Elsevier]
日期:2017-05-01
卷期号:19 (6): 1189-1201
被引量:1437
标识
DOI:10.1016/j.celrep.2017.04.031
摘要
PD-L1 and PD-L2 are ligands for the PD-1 immune inhibiting checkpoint that can be induced in tumors by interferon exposure, leading to immune evasion. This process is important for immunotherapy based on PD-1 blockade. We examined the specific molecules involved in interferon-induced signaling that regulates PD-L1 and PD-L2 expression in melanoma cells. These studies revealed that the interferon-gamma-JAK1/JAK2-STAT1/STAT2/STAT3-IRF1 axis primarily regulates PD-L1 expression, with IRF1 binding to its promoter. PD-L2 responded equally to interferon beta and gamma and is regulated through both IRF1 and STAT3, which bind to the PD-L2 promoter. Analysis of biopsy specimens from patients with melanoma confirmed interferon signature enrichment and upregulation of gene targets for STAT1/STAT2/STAT3 and IRF1 in anti-PD-1-responding tumors. Therefore, these studies map the signaling pathway of interferon-gamma-inducible PD-1 ligand expression.
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