PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
February 11, 2026Diabetes2 citations

Distinct Enterovirus Antigen Landscape in Children With Islet Autoimmunity

View Full Paper
BDBeatriz Delgado-CorralesLFLegana C H W FingerhutLPLeung Preston

Key Points

  • This research aims to explore the role of host-specific immune responses to enteroviruses in the onset of islet autoimmunity in children.
  • Used virome-wide serological profiling (VirScan) to analyze antibody responses.
  • Compared enterovirus antibody landscapes in IA-positive and IA-negative children across two cohorts.
  • Focused on samples from the time of seroconversion to track changes in immune responses.
  • Identified a distinct EV-specific antibody signature in IA-positive children.
  • A specific immunogenic hotspot was localized within the 3D RNA-dependent RNA polymerase region.
  • Male children with IA showed significantly higher antibody responses against VP1 compared to IA-negative counterparts.

Abstract

Enteroviruses (EVs) have long been implicated in the development of islet autoimmunity (IA) and type 1 diabetes. However, given the ubiquity of EV infections in children, disease susceptibility is likely driven by host-specific immune responses rather than viral exposure alone. To investigate the host antibody response to EVs, we used virome-wide serological profiling (VirScan) to compare the EV antigen landscapes in IA-positive case children versus IA-negative control children across two independent pediatric cohorts separated by 12 years, using samples collected at the time point of seroconversion. We identified a reproducible and distinct EV-specific antibody signature in IA-positive case samples, with an enriched immunogenic hotspot localized within a highly conserved region in the 3D RNA-dependent RNA polymerase. Additionally, IA-positive male children exhibited significantly heightened antibody responses against a motif in the VP1 capsid protein compared to IA-negative male children (RR 1.24; 95% CI 1.02, 1.52; P = 0.03). Our findings provide paradigm-shifting evidence that differential antiviral humoral responses, rather than the specific types of EV infection, play a central role in IA development, highlighting the need for an updated framework to study host-virus interactions in autoimmune pathogenesis. Article Highlights Children positive for islet autoimmunity (IA) in two different Australian cohorts showed a distinct enterovirus (EV) antibody signature against specific regions of the EV genome polyprotein. A specific motif in the 3D region of the EV polyprotein was consistently enriched across cohorts and sexes, making it a potential marker for IA onset. Anti-VP1 motif antibody levels varied by sex, with significantly elevated levels in male children linked to early IA onset highlighting possible sex-specific antiviral immunity. Findings support that host immune responses against EVs drive IA development, calling for a new framework to study host-virus interactions in IA.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Delgado-Corrales et al. (2026) studied this question.

synapsesocial.com/papers/698c1ca1267fb587c655f315https://doi.org/10.2337/db25-0805
Ask AI
Helpful
Bookmark
Share
View Full Paper