Strong Association of Autoantibodies Targeting Deamidated Extracellular Epitopes of Insulinoma Antigen-2 With Clinical Onset of Type 1 Diabetes

CD4+ T cells from patients with type 1 diabetes (T1D) have a significant response to post-translationally modified (PTM) deamidated IA-2 peptides; autoantibodies to these PTM neoepitopes remain to be identified in T1D. We aimed to identify autoantibodies specifically targeting reported T-cell reactive, deamidated epitopes of IA-2 and explore their relationship with T1D development. Autoantibodies to deamidated IA-2 were specific to deamidated epitopes and were predominantly present during the late stages of T1D development, challenging the hypothesis that the loss of immune tolerance occurs via post-translational modification of islet antigens. Newly identified autoantibodies to deamidated IA-2 are new biomarkers of islet autoimmunity and have the potential to aid in T1D diagnosis.

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Publication Details

Journal
Diabetes
Published
2025-01-16
DOI
https://doi.org/10.2337/db24-0571
Citations
2
Primary Topic
Diabetes and associated disorders
Type
article
Field-Weighted Citation Impact
3.63

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article

Strong Association of Autoantibodies Targeting Deamidated Extracellular Epitopes of Insulinoma Antigen-2 With Clinical Onset of Type 1 Diabetes

Xiaofan Jia, Aaron W. Michels, Liping Yu, Caiguo Zhang et al.
2 citations
Diabetes
Diabetes and associated disorders
3.63
article

Strong Association of Autoantibodies Targeting Deamidated Extracellular Epitopes of Insulinoma Antigen-2 With Clinical Onset of Type 1 Diabetes

Xiaofan Jia, Aaron W. Michels, Liping Yu, Caiguo Zhang, Janet M. Wenzlau, Fran Dong, Marian Rewers, R. D. G. Leslie, Kathleen Waugh
article en
2 citations

Abstract

CD4+ T cells from patients with type 1 diabetes (T1D) have a significant response to post-translationally modified (PTM) deamidated IA-2 peptides; autoantibodies to these PTM neoepitopes remain to be identified in T1D. We aimed to identify autoantibodies specifically targeting reported T-cell reactive, deamidated epitopes of IA-2 and explore their relationship with T1D development. Autoantibodies to deamidated IA-2 were specific to deamidated epitopes and were predominantly present during the late stages of T1D development, challenging the hypothesis that the loss of immune tolerance occurs via post-translational modification of islet antigens. Newly identified autoantibodies to deamidated IA-2 are new biomarkers of islet autoimmunity and have the potential to aid in T1D diagnosis.

DiabetesVol. 74(4)
Queen Mary University of London (GB), University of Colorado Anschutz Medical Campus (US), University of Colorado Denver (US)
National Institutes of Health
Good health and well-being
Openalex Percentile: Top 10%
Diabetes and associated disorders
3.63
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