Assessing extracellular vesicle proteins as predictive biomarkers for developing type 1 diabetes

Type 1 diabetes (T1D) is a disease characterized by the body's inability to produce insulin and consequently, to control blood glucose levels. Despite the initial trigger being unclear, the disease development process involves an autoimmune response to the islets of Langerhans, resulting in the death of insulin-producing β cells. There is no cure for the disease, and treatment relies on exogenous administration of insulin. Therefore, preventive therapies that block the autoimmune process are attractive for treating T1D. In fact, anti-CD3 antibody (Teplizumab) delays the onset of T1D by 2 years by targeting T cells. Predictive biomarkers for developing T1D are needed to aid the development and implementation of new therapies and to identify the initial trigger and mechanisms of the islet autoimmune process. In this paper, we assess the potential of plasma extracellular vesicle (EV) proteomics analysis for identifying predictive biomarkers of T1D. Our results show excellent potential of the approach, opening opportunities to perform broader studies to identify biomarkers for developing T1D.

Authors

Institutions

Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-02-09
DOI
https://doi.org/10.64898/2026.02.06.703600
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Assessing extracellular vesicle proteins as predictive biomarkers for developing type 1 diabetes

Raghavendra G. Mirmira, Panshak Dakup, Javier E. Flores, Thomas Metz et al.
bioRxiv (Cold Spring Harbor Laboratory)
Extracellular vesicles in disease
article

Assessing extracellular vesicle proteins as predictive biomarkers for developing type 1 diabetes

Raghavendra G. Mirmira, Panshak Dakup, Javier E. Flores, Thomas Metz, Lisa Bramer, Ivo Diaz Ludovico, Emily Kristen Sims, Ernesto S Nakayasu
article en

Abstract

Type 1 diabetes (T1D) is a disease characterized by the body's inability to produce insulin and consequently, to control blood glucose levels. Despite the initial trigger being unclear, the disease development process involves an autoimmune response to the islets of Langerhans, resulting in the death of insulin-producing β cells. There is no cure for the disease, and treatment relies on exogenous administration of insulin. Therefore, preventive therapies that block the autoimmune process are attractive for treating T1D. In fact, anti-CD3 antibody (Teplizumab) delays the onset of T1D by 2 years by targeting T cells. Predictive biomarkers for developing T1D are needed to aid the development and implementation of new therapies and to identify the initial trigger and mechanisms of the islet autoimmune process. In this paper, we assess the potential of plasma extracellular vesicle (EV) proteomics analysis for identifying predictive biomarkers of T1D. Our results show excellent potential of the approach, opening opportunities to perform broader studies to identify biomarkers for developing T1D.

bioRxiv (Cold Spring Harbor Laboratory)
Pacific Northwest National Laboratory (US), University of Chicago (US), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US)
U.S. Department of Energy, Battelle, Human Islet Research Network, National Institute of Diabetes and Digestive and Kidney Diseases, Pacific Northwest National Laboratory
Openalex Percentile: Top 61%
Extracellular vesicles in disease
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.