Immunoglobulin G4 in eosinophilic esophagitis: Immune complex formation and correlation with disease activity

Author:

Medernach Jonathan G.1,Li Rung‐Chi2,Zhao Xiao‐Yu3,Yin Bocheng3,Noonan Emily A.2,Etter Elaine F.2,Raghavan Shyam S.4,Borish Larry C.2,Wilson Jeffrey M.2,Barnes Barrett H.1,Platts‐Mills Thomas A. E.2ORCID,Ewald Sarah E.3,Sauer Bryan G.5,McGowan Emily C.26ORCID

Affiliation:

1. Division of Pediatric Gastroenterology and Hepatology University of Virginia School of Medicine Charlottesville Virginia USA

2. Division of Allergy and Immunology University of Virginia School of Medicine Charlottesville Virginia USA

3. Department of Microbiology, Immunology and Cancer Biology and The Carter Immunology Center University of Virginia School of Medicine Charlottesville Virginia USA

4. Department of Pathology University of Virginia School of Medicine Charlottesville Virginia USA

5. Division of Gastroenterology and Hepatology University of Virginia School of Medicine Charlottesville Virginia USA

6. Division of Allergy and Clinical Immunology Johns Hopkins University School of Medicine Baltimore Maryland USA

Abstract

AbstractBackgroundRecent studies have shown deposition of immunoglobulin G4 (IgG4) and food proteins in the esophageal mucosa of eosinophilic esophagitis (EoE) patients. Our aims were to assess whether co‐localization of IgG4 and major cow's milk proteins (CMPs) was associated with EoE disease activity and to investigate the proteins enriched in proximity to IgG4 deposits.MethodsThis study included adult subjects with EoE (n = 13) and non‐EoE controls (n = 5). Esophageal biopsies were immunofluorescence stained for IgG4 and CMPs. Co‐localization in paired samples from active disease and remission was assessed and compared to controls. The proteome surrounding IgG4 deposits was evaluated by the novel technique, AutoSTOMP. IgG4‐food protein interactions were confirmed with co‐immunoprecipitation and mass spectrometry.ResultsIgG4‐CMP co‐localization was higher in the active EoE group compared to paired remission samples (Bos d 4, p = .02; Bos d 5, p = .002; Bos d 8, p = .002). Co‐localization was also significantly higher in the active EoE group compared to non‐EoE controls (Bos d 4, p = .0013; Bos d 5, p = .0007; Bos d 8, p = .0013). AutoSTOMP identified eosinophil‐derived proteins (PRG 2 and 3, EPX, RNASE3) and calpain‐14 in IgG4‐enriched areas. Co‐immunoprecipitation and mass spectrometry confirmed IgG4 binding to multiple food allergens.ConclusionThese findings further contribute to the understanding of the interaction of IgG4 with food antigens as it relates to EoE disease activity. These data strongly suggest the immune complex formation of IgG4 and major cow's milk proteins. These immune complexes may have a potential role in the pathophysiology of EoE by contributing to eosinophil activation and disease progression.

Funder

American College of Gastroenterology

National Center for Advancing Translational Sciences

National Institute of Biomedical Imaging and Bioengineering

National Institute of Allergy and Infectious Diseases

National Institute of General Medical Sciences

National Institutes of Health

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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