封锁
癌症研究
免疫疗法
免疫系统
医学
生物
受体
免疫学
内科学
作者
Wei Yao,Xiaoxin Ren,Phillip M. Galbo,Scott Moerdler,Hao Wang,R. Alejandro Sica,Bijan Etemad-Gilbertson,Lei Shi,Liqiang Zhu,Xu-Dong Tang,Lin Qi,Mou Peng,Fangxia Guan,Deyou Zheng,Jordan M. Chinai,Xingxing Zang
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2021-07-09
卷期号:6 (61)
被引量:59
标识
DOI:10.1126/sciimmunol.abf9792
摘要
The B7 family ligand HERV-H LTR-associating protein 2 (HHLA2) is an attractive target for cancer immunotherapy because of its coinhibitory function, overexpression in human cancers, and association with poor prognoses. However, the knowledge of the HHLA2 pathway is incomplete. HHLA2 has an established positive receptor transmembrane and immunoglobulin (Ig) domain containing 2 (TMIGD2) but a poorly characterized negative receptor human killer cell Ig-like receptor, three Ig domains, and long cytoplasmic tail (KIR3DL3). Here, KIR3DL3 and TMIGD2 simultaneously bound to different sites of HHLA2. KIR3DL3 was mainly expressed on CD56
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