提吉特
单克隆抗体
抗体
贪婪
平移(音频)
癌症研究
抗体依赖性细胞介导的细胞毒性
免疫学
生物
免疫系统
体内
免疫疗法
镜头(地质)
缩放
生物技术
古生物学
作者
Dong Han,Yinfeng Xu,Xinping Zhao,Yunyun Mao,Qinglin Kang,Weihong Wen,Xiaoyan Yu,Lei Xu,Fujia Liu,Mengyao Zhang,Jiazhen Cui,Zhang Wang,Yang Zhixin,Peng Du,Weijun Qin
标识
DOI:10.1016/j.bbrc.2020.12.013
摘要
TIGIT is an emerging novel checkpoint target that is expressed on both tumor-infiltrating T cells and NK cells. Some current investigational antibodies targeting TIGIT have also achieved dramatic antitumor efficacy in late clinical research. Most recently, the relevance of NK cell–associated TIGIT signaling pathway to tumors’ evasion of the immune system has been clearly revealed, which endows NK cells with a pivotal role in the therapeutic effects of TIGIT blockade. In this article, we describe a novel anti-TIGIT monoclonal antibody, AET2010, which was acquired from a phage-displayed human single-chain antibody library through a cell panning strategy. With emphasis on its regulation of NK cells, we confirmed the excellent ex vivo and in vivo antitumor immunity of AET2010 mediated by the NK-92MI cells. Intriguingly, our work also revealed that AET2010 displays a lower affinity but parallel avidity and activity relative to MK7684, an investigational monoclonal antibody from MSD, implying a reasonable balance of potency and potential side effects for AET2010. Together, these results are promising and warrant further development of AET2010.
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