CD8型
生物
免疫学
主要组织相容性复合体
细胞毒性T细胞
T细胞
点头
免疫系统
小岛
抗原
MHC I级
细胞生物学
糖尿病
内分泌学
遗传学
体外
作者
Lina Wang,Jie Li,Shushu Yang,Gang Meng,Xiaoling Chen,Zhang Mengjun,Wang Shufeng,Xiangqian Li,Yuzhang Wu,Li Wang
出处
期刊:Research Square - Research Square
日期:2023-06-09
标识
DOI:10.21203/rs.3.rs-2997556/v1
摘要
Abstract Autoreactive CD8+ T cells play a key role in type 1 diabetes (T1D), but the antigen spectrum that activates autoreactive CD8+ T cells remains unclear. Endoplasmic reticulum stress (ERS) has been implicated in β cell autoantigen generation. Here, we analyzed the major histocompatibility complex class I (MHC-I)-associated immunopeptidome (MIP) of islet β cells under steady-state and ERS conditions and found a small number of peptides that were exclusively present in the MIP of the ERS-exposed β cell line. Among them, OTUB258 − 66 showed immunodominance, and the corresponding autoreactive CD8+ T cells were diabetogenic in NOD mice. High glucose intake upregulated pancreatic OTUB2 expression and amplified the OTUB258 − 66-specific CD8+ T-cell response in NOD mice. Repeated OTUB258 − 66 administration significantly reduced the T1D incidence in these mice. This study provides novel β cell autoantigens for developing specific immune interventions for T1D prevention and treatment. Data are available via ProteomeXchange with identifier PXD041227.
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