| Literature DB >> 31495780 |
Yanni Zhu1, Drake J Smith1, Yang Zhou1, Yan-Ruide Li1, Jiaji Yu1, Derek Lee1, Yu-Chen Wang1, Stefano Di Biase1, Xi Wang1, Christian Hardoy1, Josh Ku1, Tasha Tsao1, Levina J Lin1, Alexander T Pham1, Heesung Moon1, Jami McLaughlin1, Donghui Cheng1, Roger P Hollis1, Beatriz Campo-Fernandez1, Fabrizia Urbinati1, Liu Wei2, Larry Pang2, Valerie Rezek3, Beata Berent-Maoz4, Mignonette H Macabali4, David Gjertson5, Xiaoyan Wang4, Zoran Galic3, Scott G Kitchen3, Dong Sung An6, Siwen Hu-Lieskovan4, Paula J Kaplan-Lefko7, Satiro N De Oliveira8, Christopher S Seet3, Sarah M Larson9, Stephen J Forman10, James R Heath11, Jerome A Zack12, Gay M Crooks13, Caius G Radu14, Antoni Ribas15, Donald B Kohn16, Owen N Witte17, Lili Yang18.
Abstract
Invariant natural killer T (iNKT) cells are potent immune cells for targeting cancer; however, their clinical appli<span class="Gene">cation 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.Entities:
Keywords: HSC; HSC transfer; HSCT; T cell receptor; TCR; cancer immunotherapy; cell therapy; gene therapy; hematopoietic stem cell; iNKT; invariant natural killer T cell; preclinical development; sr39TK suicide gene; stem cell therapy
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Year: 2019 PMID: 31495780 PMCID: PMC7018522 DOI: 10.1016/j.stem.2019.08.004
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633