| Literature DB >> 33963786 |
Kin Man Au1,2, Yusra Medik1,2, Qi Ke3,4, Roland Tisch3,4, Andrew Z Wang1,2,4.
Abstract
Type 1 diabetes mellitus (T1DM) is a chronic autoimmune disease that results from autoreactive T cells destroying insulin-producing pancreatic beta (β) cells. The development of T1DM is associated with the deficiency of co-inhibitory immune checkpoint ligands (e.g., PD-L1, CD86, and Gal-9) in β cells. Here, a new translational approach based on metabolic glycoengineering and bioorthogonal click chemistry, which bioengineers β cells with co-inhibitory immune checkpoint molecules that induce antigen-specific immunotolerance and reverse early-onset hyperglycemia is reported. To achieve this goal, a subcutaneous injectable acellular pancreatic extracellular matrix platform for localizing the bioengineered β cells while creating a pancreas-like immunogenic microenvironment, in which the autoreactive T cells can interface with the β cells, is devised.Entities:
Keywords: bioorthogonal click chemistry; dendrimers; extracellular matrix; immune checkpoint; metabolic glycoengineering; type 1 diabetes
Mesh:
Year: 2021 PMID: 33963786 PMCID: PMC8222180 DOI: 10.1002/adma.202101253
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 32.086