← 返回

靶向 B7H3 的 CAR-T 细胞在胃癌中的抗肿瘤反应

英文原题:Antitumor responses in gastric cancer by targeting B7H3 via chimeric antigen receptor T cells.

查看英文原题

Antitumor responses in gastric cancer by targeting B7H3 via chimeric antigen receptor T cells.

PubMed 2022/01/31(内容时间) Cancer Cell Int Q1 · IF 7(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

我们的研究表明,B7H3 是 GC 治疗的一个有吸引力的靶点,且 B7H3 具有很高的临床应用潜力。

研究思路结论见上方概要

胃癌(GC)预后差,治疗选择有限。作为一种新的有前景的癌症治疗方法,嵌合抗原受体(CAR)-T细胞代表了潜在的GC治疗手段。我们研究了靶向B7H3的CAR-T 细胞在GC中的抗肿瘤活性。

在我们的研究中,检测了B7H3在GC组织中的表达,并探索了靶向B7H3的CAR-T 细胞在GC中的杀肿瘤潜力。构建了具有人源化抗原识别结构域的B7H3导向CAR-T 细胞。最终在体外和体内研究了该CAR-T 细胞的抗肿瘤效果。

我们的结果表明,B7H3靶向的CAR-T 细胞有效杀伤了GC肿瘤细胞。此外,我们发现B7H3与肿瘤细胞干性相关,抗B7H3 CAR-T 可以同时靶向干细胞样GC细胞以改善治疗结果。

展开英文摘要原文

Gastric cancer (GC) has a poor prognosis and limited therapeutic options. As a new promising cancer therapeutic approach, chimeric antigen receptor (CAR)-T cells represent a potential GC treatment. We investigated the antitumor activity of CAR-T cells target-B7H3 in GC.

In our study, expression of B7H3 was examined in GC tissues and explored the tumoricidal potential of B7H3-targeting CAR-T cells in GC. B7H3-directed CAR-T cells with a humanized antigen-recognizing domain was generated. The anti-tumor effects of this CAR-T cell were finally investigated in vitro and in vivo.

Our results show that B7H3-directed CAR-T cells efficiently killed GC tumor cells. In addition, we found that B7H3 is correlated with tumor cell stemness, and anti-B7H3 CAR-T can simultaneously target stem cell-like GC cells to improve the treatment outcome.

Our study indicates that B7H3 is an attractive target for GC therapy, and B7H3 has high potential for clinical application.

论文信息

作者
Sun F、Yu X、Ju R、Wang Z、Wang Y
第一作者单位
Department of Clinical Laboratory, Weifang People's Hospital, Weifang, 261000, Shandong, China.China
通讯作者单位
Department of Clinical Laboratory, Weifang People's Hospital, Weifang, 261000, Shandong, China. Wangyuhui_wfrm@163.com.China
期刊
Cancer cell international2022 Jan 31
原文标识
PubMed 35101032 · DOI 10.1186/s12935-022-02471-8