中文摘要
CD1d限制性恒定NKT(iNKT)细胞在肿瘤免疫中发挥关键作用。然而,其数量稀少且持久性有限,限制了其开发和临床应用。在此,我们证明,使用改良的细胞因子组合可从外周血单个核细胞中高效扩增iNKT细胞。引入IL-21显著提高了CD62L阳性记忆样iNKT细胞的比例。装备B7H3靶向第二代CAR和IL-21的iNKT细胞显示出强效的肿瘤细胞杀伤活性。此外,IL-21的共表达促进了Stat3信号通路的激活,并在体外降低了CAR-iNKT细胞中耗竭标志物的表达。最重要的是,IL-21装备显著延长了B7H3 CAR-iNKT细胞在体内的增殖和存活,从而提高了其在小鼠肾癌异种移植模型中的治疗效果,且未观察到细胞因子相关不良事件。总之,这些结果表明,装备IL-21的B7H3 CAR-iNKT是一种有前景的癌症治疗策略。
展开英文摘要原文
CD1d-restricted invariant NKT (iNKT) cells play a critical role in tumor immunity.
However, the scarcity and limited persistence restricts their development and clinical application.
Here, we demonstrated that iNKT cells could be efficiently expanded using modified cytokines combination from peripheral blood mononuclear cells. Introduction of IL-21 significantly increased the frequency of CD62L-positive memory-like iNKT cells. iNKT cells armoring with B7H3-targeting second generation CAR and IL-21 showed potent tumor cell killing activity.
Moreover, co-expression of IL-21 promoted the activation of Stat3 signaling and reduced the expression of exhaustion markers in CAR-iNKT cells in vitro . Most importantly, IL-21-arming significantly prolonged B7H3 CAR-iNKT cell proliferation and survival in vivo , thus improving their therapeutic efficacy in mouse renal cancer xerograph models without observed cytokine-related adverse events. In summary, these results suggest that B7H3 CAR-iNKT armored with IL-21 is a promising therapeutic strategy for cancer treatment.
论文信息
- 作者
- Liu Y、Dang Y、Zhang C、Liu L、Cai W、Li L、Fang L、Wang M
- 单位
- Cancer Institute, Xuzhou Medical University, 209 Tongshan Road, Xuzhou, Jiangsu 221004, China.China
- 期刊
- iScience2024 Jan 19