肝细胞癌
癌症研究
医学
免疫学
伊立替康
药理学
癌症
生物
抗体
内科学
结直肠癌
作者
Xin Chen,Yanmin Chen,Rong Liang,Lanxin Xiang,Jingwen Li,Yuankui Zhu,Huixia He,Le Huang,Dianbao Zuo,Weihang Li,Xinjun Liang,Shuang Dong,Sheng Hu,Mitchell Ho,Mingqian Feng
标识
DOI:10.1158/1535-7163.mct-20-1025
摘要
xenograft mouse studies demonstrated that all bispecific antibodies suppressed tumor growth similarly, with hYP7-OKT3-hFc performing slightly better. Combination of hYP7-OKT3-hFc with Irinotecan dramatically improved the efficacy and arrested tumor growth of HepG2, Hep3B, and G1 in xenograft mice. Our results demonstrated that the cell surface proximal bispecific antibody hYP7-OKT3-hFc was superior in terms of potency and the GPC3-targeted bispecific antibody combined with Irinotecan was much potent to control HCC growth.
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