Development of Hematopoietic Stem Cell-Engineered Invariant Natural Killer T Cell Therapy for Cancer

利用造血干细胞工程改造的不变自然杀伤T细胞疗法治疗癌症

阅读:3
作者:Yanni Zhu,Drake J Smith,Yang Zhou,Yan-Ruide Li,Jiaji Yu,Derek Lee,Yu-Chen Wang,Stefano Di Biase,Xi Wang,Christian Hardoy,Josh Ku,Tasha Tsao,Levina J Lin,Alexander T Pham,Heesung Moon,Jami McLaughlin,Donghui Cheng,Roger P Hollis,Beatriz Campo-Fernandez,Fabrizia Urbinati,Liu Wei,Larry Pang,Valerie Rezek,Beata Berent-Maoz,Mignonette H Macabali,David Gjertson,Xiaoyan Wang,Zoran Galic,Scott G Kitchen,Dong Sung An,Siwen Hu-Lieskovan,Paula J Kaplan-Lefko,Satiro N De Oliveira,Christopher S Seet,Sarah M Larson,Stephen J Forman,James R Heath,Jerome A Zack,Gay M Crooks,Caius G Radu,Antoni Ribas,Donald B Kohn,Owen N Witte,Lili Yang

Abstract

Invariant natural killer T (iNKT) cells are potent immune cells for targeting cancer; however, their clinical application has been hindered by their low numbers in cancer patients. Here, we developed a proof-of-concept for hematopoietic stem cell-engineered iNKT (HSC-iNKT) cell therapy with the potential to provide therapeutic levels of iNKT cells for a patient's lifetime. Using a human HSC engrafted mouse model and a human iNKT TCR gene engineering approach, we demonstrated the efficient and long-term generation of HSC-iNKT cells in vivo. These HSC-iNKT cells closely resembled endogenous human iNKT cells, could deploy multiple mechanisms to attack tumor cells, and effectively suppressed tumor growth in vivo in multiple human tumor xenograft mouse models. Preclinical safety studies showed no toxicity or tumorigenicity of the HSC-iNKT cell therapy. Collectively, these results demonstrated the feasibility, safety, and cancer therapy potential of the proposed HSC-iNKT cell therapy and laid a foundation for future clinical development.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。