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Identification of Autoantibodies to a Hybrid Insulin Peptide in Type 1 Diabetes

Type 1 diabetes (T1D) is a chronic autoimmune disease that attacks the insulin-producing b cells of the pancreatic islets. Autoantibodies to b cell proteins typically appear in the circulation years before disease onset, and serve as the most accurate biomarkers of T1D risk. Our laboratory has recen...

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Autores principales: Wenzlau, Janet M., Gu, Yong, Michels, Aaron, Rewers, Marian, Haskins, Kathryn, Yu, Liping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487141/
https://www.ncbi.nlm.nih.gov/pubmed/37685398
http://dx.doi.org/10.3390/diagnostics13172859
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author Wenzlau, Janet M.
Gu, Yong
Michels, Aaron
Rewers, Marian
Haskins, Kathryn
Yu, Liping
author_facet Wenzlau, Janet M.
Gu, Yong
Michels, Aaron
Rewers, Marian
Haskins, Kathryn
Yu, Liping
author_sort Wenzlau, Janet M.
collection PubMed
description Type 1 diabetes (T1D) is a chronic autoimmune disease that attacks the insulin-producing b cells of the pancreatic islets. Autoantibodies to b cell proteins typically appear in the circulation years before disease onset, and serve as the most accurate biomarkers of T1D risk. Our laboratory has recently discovered novel b cell proteins comprising hybrid proinsulin:islet amyloid polypeptide peptides (IAPP). T cells from a diabetic mouse model and T1D patients are activated by these hybrid peptides. In this study, we asked whether these hybrid molecules could serve as antigens for autoantibodies in T1D and prediabetic patients. We analyzed sera from T1D patients, prediabetics and healthy age-matched donors. Using a highly sensitive electrochemiluminescence assay, sera were screened for binding to recombinant proinsulin:IAPP probes or truncated derivatives. Our results show that sera from T1D patients contain antibodies that bind larger hybrid proinsulin:IAPP probes, but not proinsulin or insulin, at significantly increased frequencies compared to normal donors. Examination of sera from prediabetic patients confirms titers of antibodies to these hybrid probes in more than 80% of individuals, often before seroconversion. These results suggest that hybrid insulin peptides are common autoantigens in T1D and prediabetic patients, and that antibodies to these peptides may serve as valuable early biomarkers of the disease.
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spelling pubmed-104871412023-09-09 Identification of Autoantibodies to a Hybrid Insulin Peptide in Type 1 Diabetes Wenzlau, Janet M. Gu, Yong Michels, Aaron Rewers, Marian Haskins, Kathryn Yu, Liping Diagnostics (Basel) Article Type 1 diabetes (T1D) is a chronic autoimmune disease that attacks the insulin-producing b cells of the pancreatic islets. Autoantibodies to b cell proteins typically appear in the circulation years before disease onset, and serve as the most accurate biomarkers of T1D risk. Our laboratory has recently discovered novel b cell proteins comprising hybrid proinsulin:islet amyloid polypeptide peptides (IAPP). T cells from a diabetic mouse model and T1D patients are activated by these hybrid peptides. In this study, we asked whether these hybrid molecules could serve as antigens for autoantibodies in T1D and prediabetic patients. We analyzed sera from T1D patients, prediabetics and healthy age-matched donors. Using a highly sensitive electrochemiluminescence assay, sera were screened for binding to recombinant proinsulin:IAPP probes or truncated derivatives. Our results show that sera from T1D patients contain antibodies that bind larger hybrid proinsulin:IAPP probes, but not proinsulin or insulin, at significantly increased frequencies compared to normal donors. Examination of sera from prediabetic patients confirms titers of antibodies to these hybrid probes in more than 80% of individuals, often before seroconversion. These results suggest that hybrid insulin peptides are common autoantigens in T1D and prediabetic patients, and that antibodies to these peptides may serve as valuable early biomarkers of the disease. MDPI 2023-09-04 /pmc/articles/PMC10487141/ /pubmed/37685398 http://dx.doi.org/10.3390/diagnostics13172859 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wenzlau, Janet M.
Gu, Yong
Michels, Aaron
Rewers, Marian
Haskins, Kathryn
Yu, Liping
Identification of Autoantibodies to a Hybrid Insulin Peptide in Type 1 Diabetes
title Identification of Autoantibodies to a Hybrid Insulin Peptide in Type 1 Diabetes
title_full Identification of Autoantibodies to a Hybrid Insulin Peptide in Type 1 Diabetes
title_fullStr Identification of Autoantibodies to a Hybrid Insulin Peptide in Type 1 Diabetes
title_full_unstemmed Identification of Autoantibodies to a Hybrid Insulin Peptide in Type 1 Diabetes
title_short Identification of Autoantibodies to a Hybrid Insulin Peptide in Type 1 Diabetes
title_sort identification of autoantibodies to a hybrid insulin peptide in type 1 diabetes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487141/
https://www.ncbi.nlm.nih.gov/pubmed/37685398
http://dx.doi.org/10.3390/diagnostics13172859
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