Treatment of hepatocellular carcinoma with a GPC3-targeted bispecific T cell engager

被引:38
作者
Bi, Yanyu [1 ]
Jiang, Hua [1 ]
Wang, Peng [2 ]
Song, Bo [2 ]
Wang, Huamao [2 ]
Kong, Xianming [3 ]
Li, Zonghai [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Canc Inst, State Key Lab Oncogenes & Related Genes, Shanghai, Peoples R China
[2] CARsgen Therapeut, Shanghai, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Renji Hosp, Shanghai, Peoples R China
关键词
hepatocellular carcinoma; glypican-3; bispecific T cell engager; immunotherapy; SINGLE-CHAIN ANTIBODY; GLYPICAN-3; EXPRESSION; SOLID TUMORS; EP-CAM; CONSTRUCT; MARKER; CANCER; BLINATUMOMAB; LYMPHOCYTES; ING-1;
D O I
10.18632/oncotarget.17905
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
There are limited strategies for the treatment of hepatocellular carcinoma (HCC). In this study, we prepared a Bispecific T cell engager (BiTE) targeting Glypican 3 (GPC3) and CD3. The GPC3/CD3 BiTE was prepared by fusing the single-chain variable fragment (scFv) of the humanized anti-GPC3 antibody (9F2) with the scFv of the anti-CD3 antibody (OKT3). The in vitro and in vivo cytotoxic activities of the GPC3/CD3 BiTE were evaluated against various HCC cell lines. The GPC3/CD3 BiTE could efficiently mediate the T cell killing of GPC3-positive HCC in vitro, which was dependent on GPC3 expression on the surface of HCC cells. Moreover, our study indicates that, in the presence of the GPC3/CD3 BiTE, T cells could efficiently destroy GPC3-positive human HCC cells in vitro and in vivo. Additionally, our study further proved that GPC3 is not expressed in normal tissues. Thus, GPC3 may be a cancer-specific antigen. Collectively, these findings suggest that this anti-GPC3 BiTE might be a promising anti-tumor reagent for patients with GPC3-positive HCC.
引用
收藏
页码:52866 / 52876
页数:11
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