NKG2D公司
抗体
CD16
免疫
细胞毒性T细胞
Fc受体
免疫系统
生物
抗体依赖性细胞介导的细胞毒性
癌症研究
免疫学
先天免疫系统
自然杀伤细胞
单克隆抗体
CD8型
体外
生物化学
CD3型
作者
Lucas Ferrari de Andrade,Rong En Tay,Deng Pan,Adrienne Luoma,Yoshinaga Ito,S Badrinath,Daphne Tsoucas,Bettina Franz,Kenneth F. May,Christopher J. Harvey,Sebastian Kobold,Jason W. Pyrdol,Charles H. Yoon,Guo‐Cheng Yuan,F. Stephen Hodi,Glenn Dranoff,Kai W. Wucherpfennig
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2018-03-29
卷期号:359 (6383): 1537-1542
被引量:423
标识
DOI:10.1126/science.aao0505
摘要
Helping NK cells find their way MICA and MICB proteins can be expressed on tumors and act as “kill me” signals to the immune system. But tumors often disguise themselves by shedding these proteins, which prevents specialized natural killer (NK) cells from recognizing and destroying the cancer. Ferrari de Andrade et al. engineered antibodies directed against the site responsible for the proteolytic shedding of MICA and MICB (see the Perspective by Cerwenka and Lanier). The approach effectively locked MICA and MICB onto tumors so that NK cells could spot them for elimination. The antibodies exhibited preclinical efficacy in multiple tumor models, including humanized melanoma. Furthermore, the strategy reduced lung cancer metastasis after NK cell–mediated tumor lysis. Science , this issue p. 1537 ; see also p. 1460
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