STAT6
转录因子
癌症研究
单克隆抗体
功能(生物学)
药效学
抗体
生物
医学
信号转导
计算生物学
生物标志物
小分子
化学
免疫学
药理学
突变
细胞生物学
抑制器
临床疗效
抄写(语言学)
炎症
生物信息学
作者
Arsalan Shabbir,Sagar Agarwal,Alice McDonald,Kelvin Shi,Annie L. Conery,Mahta Mortezavi,Nello Mainolfi,Jared Gollob,Chad Nivens
出处
期刊:Skin
[National Society for Cutaneous Medicine]
日期:2025-11-10
卷期号:9 (6): s712-s712
摘要
STAT6 is an essential transcription factor in the IL-4/IL-13 signaling pathways and the central driver of Th2 inflammation in allergic/atopic diseases. Multiple gain of function mutations of STAT6 have been identified to cause severe atopic/allergic diseases in humans. Dupilumab, an injectable monoclonal antibody that blocks IL-4/IL-13 signaling, is an approved therapy for multiple atopic/allergic diseases therefore targeting STAT6 in these diseases is supported by both human genetics and dupilumab’s clinical activity. STAT6 functions through protein-protein and protein-DNA interactions. It has been challenging to selectively and potently inhibit STAT6 with traditional small molecule inhibitors. However, STAT6 is well suited for a novel targeted protein degradation approach, where a simple binding event is sufficient to drive degradation of the protein and fully block its functions.
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