Engineering of human mesenchymal stem cells resistant to multiple natural killer subtypes
| Autor: | Dejin Zheng, Xiaoyan Wang, Zhenwu Zhang, Enqin Li, Cheungkwan Yeung, Roma Borkar, Guihui Qin, Yaojiong Wu, Ren-He Xu |
|---|---|
| Rok vydání: | 2022 |
| Předmět: |
mesenchymal stem cells
natural killer cells Tissue Engineering Cell Biology Applied Microbiology and Biotechnology Cell Line Killer Cells Natural Humans immune rejection Human embryonic stem cells beta 2-Microglobulin innate immunity Molecular Biology Ecology Evolution Behavior and Systematics Research Paper Developmental Biology |
| Zdroj: | International Journal of Biological Sciences |
| ISSN: | 1449-2288 |
| Popis: | Mesenchymal stem cells (MSCs) as a therapeutic promise are often quickly cleared by innate immune cells of the host including natural killer (NK) cells. Efforts have been made to generate immune-escaping human embryonic stem cells (hESCs) where T cell immunity is evaded by defecting β-2-microglobulin (B2M), a common unit for human leukocyte antigen (HLA) class I, and NK cells are inhibited via ectopic expression of HLA-E or -G. However, NK subtypes vary among recipients and even at different pathologic statuses. It is necessary to dissect and optimize the efficacy of the immune-escaping cells against NK subtypes. Here, we first generated B2M knockout hESCs and differentiated them to MSCs (EMSCs) and found that NK resistance occurred with B2M-/- EMSCs expressing HLA-E and -G only when they were transduced via an inducible lentiviral system in a dose-dependent manner but not when they were inserted into a safe harbor. HLA-E and -G expressed at high levels together in transduced EMSCs inhibited three major NK subtypes, including NKG2A+/LILRB1+, NKG2A+/LILRB1-, and NKG2A-/LILRB1+, which was further potentiated by IFN-γ priming. Thus, this study engineers MSCs with resistance to multiple NK subtypes and underscores that dosage matters when a transgene is used to confer a novel effect to host cells, especially for therapeutic cells to evade immune rejection. |
| Databáze: | OpenAIRE |
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