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Immune Checkpoint‐Bioengineered Beta Cell Vaccine Reverses Early‐Onset Type 1 Diabetes
Author(s) -
Au Kin Man,
Medik Yusra,
Ke Qi,
Tisch Roland,
Wang Andrew Z.
Publication year - 2021
Publication title -
advanced materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.707
H-Index - 527
eISSN - 1521-4095
pISSN - 0935-9648
DOI - 10.1002/adma.202101253
Subject(s) - immune system , immune checkpoint , immunology , cancer research , microbiology and biotechnology , biology , immunotherapy
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.