Engineered PD-L1-Expressing Platelets Reverse New-Onset Type 1 Diabetes

© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 32(2020), 26 vom: 04. Juli, Seite e1907692
1. Verfasser: Zhang, Xudong (VerfasserIn)
Weitere Verfasser: Kang, Yang, Wang, Jinqiang, Yan, Junjie, Chen, Qian, Cheng, Hao, Huang, Peng, Gu, Zhen
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2020
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article drug delivery immune tolerance platelets programmed death-ligand 1 (PD-L1) type 1 diabetes (T1D) B7-H1 Antigen Blood Glucose Insulin
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520 |a The pathogenesis of Type 1 diabetes (T1D) arises from the destruction of insulin-producing β-cells by islet-specific autoreactive T cells. Inhibition of islet-specific autoreactive T cells to rescue β-cells is a promising approach to treat new-onset T1D. The immune checkpoint signal axis programmed death-1/programmed death-ligand 1 (PD-1/PD-L1) can effectively regulate the activity of T cells and prevent autoimmune attack. Here, megakaryocyte progenitor cells are genetically engineered to overexpress PD-L1 to produce immunosuppressive platelets. The PD-L1-overexpressing platelets (designated PD-L1 platelets) accumulate in the inflamed pancreas and may suppress the activity of pancreas autoreactive T cells in newly hyperglycemic non-obese diabetic (NOD) mice, protecting the insulin-producing β-cells from destruction. Moreover, PD-L1 platelet treatment also increases the percentage of the regulatory T cells (Tregs) and maintains immune tolerance in the pancreas. It is demonstrated that the rescue of β-cells by PD-L1 platelets can effectively maintain normoglycemia and reverse diabetes in newly hyperglycemic NOD mice 
650 4 |a Journal Article 
650 4 |a drug delivery 
650 4 |a immune tolerance 
650 4 |a platelets 
650 4 |a programmed death-ligand 1 (PD-L1) 
650 4 |a type 1 diabetes (T1D) 
650 7 |a B7-H1 Antigen  |2 NLM 
650 7 |a Blood Glucose  |2 NLM 
650 7 |a Insulin  |2 NLM 
700 1 |a Kang, Yang  |e verfasserin  |4 aut 
700 1 |a Wang, Jinqiang  |e verfasserin  |4 aut 
700 1 |a Yan, Junjie  |e verfasserin  |4 aut 
700 1 |a Chen, Qian  |e verfasserin  |4 aut 
700 1 |a Cheng, Hao  |e verfasserin  |4 aut 
700 1 |a Huang, Peng  |e verfasserin  |4 aut 
700 1 |a Gu, Zhen  |e verfasserin  |4 aut 
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773 1 8 |g volume:32  |g year:2020  |g number:26  |g day:04  |g month:07  |g pages:e1907692 
856 4 0 |u http://dx.doi.org/10.1002/adma.201907692  |3 Volltext 
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