Lymphadenopathy in IgG4-related disease: a phenotype of severe activity and poor prognosis, with eotaxin-3 as a new biomarker

Rheumatology (Oxford). 2021 Feb 1;60(2):967-975. doi: 10.1093/rheumatology/keaa648.

Abstract

Objective: To clarify relevant proteins and clinical characteristics of a phenotype of IgG4-related disease (IgG4-RD) with lymphadenopathy.

Methods: We enrolled patients newly diagnosed with IgG4-RD in our department between January 2000 and June 2018 and performed proteomic analysis to measure serum concentrations of 1305 proteins. We extracted proteins overexpressed in patients with IgG4-RD with lymphadenopathy by comparing between those with lymphadenopathy, those without lymphadenopathy and healthy controls. We further reviewed all the patients with IgG4-RD in our institution and investigated the characteristics and prognosis of the patients with IgG4-RD with lymphadenopathy.

Results: Eighty-five patients with IgG4-RD were enrolled, of which, 55% had lymphadenopathy. Proteomic analysis in 31 patients with IgG4-RD and 6 healthy controls revealed that eotaxin-3 was a potential serum biomarker in the patients with lymphadenopathy versus those without lymphadenopathy and healthy controls. A cohort of 85 patients with IgG4-RD demonstrated that patients with lymphadenopathy showed a significantly higher serum IgG4, IgG4:IgG ratio, IgG4-RD responder index and eosinophilia (P < 0.001 for all), irrelevant of the extent to which organ involvement developed. Patients with lymphadenopathy treated with glucocorticoid alone relapsed with significantly higher rates than those without lymphadenopathy (P = 0.03).

Conclusion: Lymphadenopathy in IgG4-RD represents a phenotype associated with high disease activities, eosinophilia and relapsing disease. Eotaxin-3 is a novel biomarker related to IgG4-RD with lymphadenopathy.

Keywords: IgG4-related disease; biomarker; eosinophilia; eotaxin-3; lymphadenopathy; relapse.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / blood
  • Chemokine CCL26 / blood*
  • Correlation of Data
  • Eosinophilia / diagnosis
  • Eosinophilia / etiology
  • Female
  • Gene Expression Profiling / methods*
  • Humans
  • Immunoglobulin G4-Related Disease* / blood
  • Immunoglobulin G4-Related Disease* / diagnosis
  • Immunoglobulin G4-Related Disease* / physiopathology
  • Lymphadenopathy* / diagnosis
  • Lymphadenopathy* / etiology
  • Lymphadenopathy* / immunology
  • Male
  • Middle Aged
  • Patient Acuity
  • Recurrence
  • Up-Regulation

Substances

  • Biomarkers
  • Chemokine CCL26