Converting Tumoral PD-L1 into a 4-1BB Agonist for Safer and More Effective Cancer Immunotherapy

被引:4
|
作者
Li, Zihai [1 ,2 ]
Azar, Joseph H. [1 ,2 ]
Rubinstein, Mark P. [1 ,2 ]
机构
[1] Ohio State Univ, Div Med Oncol, Dept Internal Med, Columbus, OH USA
[2] Ohio State Univ, James Comprehens Canc Ctr, Plotonia Inst Immunooncol, 460 W 12th Ave,BRT 510,Biomed Res Tower, Columbus, OH 43210 USA
关键词
D O I
10.1158/2159-8290.CD-22-0219
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Dose-limiting toxicities are thought to temper the efficacy of single-agent 4-1BB agonists. To overcome this hurdle, in this issue of Cancer Discovery, Muik and colleagues report preclinical and clinical studies describing a first-in-class bispecific fusion protein targeting 4-1BB and PD-L1.
引用
收藏
页码:1184 / 1186
页数:3
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