» Articles » PMID: 22121132

IgG4 Immune Response in Churg-Strauss Syndrome

Overview
Journal Ann Rheum Dis
Specialty Rheumatology
Date 2011 Nov 29
PMID 22121132
Citations 56
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: T-helper type 2 responses are crucial in Churg-Strauss syndrome (CSS) and may enhance the production of IgG4 antibodies. The authors assessed the IgG4 immune response in CSS patients.

Methods: The authors included 46 consecutive patients with CSS (24 with active and 22 with quiescent disease), 26 with granulomatosis with polyangiitis (GPA, Wegener's), 25 with atopic asthma and 20 healthy controls and determined serum IgG, IgM, IgA, IgE and IgG subclass levels. Tissue infiltration by IgG4 plasma cells was assessed in nine patients with CSS, 10 with GPA, 22 with chronic sinusitis (11 with and 11 without eosinophilia).

Results: IgG4 levels were markedly higher in active CSS patients than in controls (p<0.001 vs all control groups). Serum IgG4 correlated with the number of disease manifestations (r=0.52, p=0.01) and the Birmingham vasculitis activity score (r=0.64, p=0.001). Longitudinal analysis in 12 CSS cases showed that both the IgG4 level and IgG4/IgG ratio dropped during disease remission (p=3×10(-5) and p=6×10(-4), respectively). Tissue analysis did not show an increased IgG4 plasma cell infiltration in CSS biopsies compared with control groups.

Conclusions: Serum IgG4 levels are markedly elevated in active CSS and correlate with the number of organ manifestations and disease activity.

Citing Articles

Heterogeneity and individualized therapy for eosinophilic granulomatosis with polyangiitis.

Hua L, Xie M Ther Adv Respir Dis. 2025; 19:17534666251318615.

PMID: 39980304 PMC: 11843704. DOI: 10.1177/17534666251318615.


Etiological study of polyclonal hypergammaglobulinemia in a French cohort of hospitalized patients and proposal of a diagnostic aid algorithm : Short title: polyclonal hypergammaglobulinemia in a French cohort of hospitalized patients.

Andre M, Contis A, Berard A Sci Rep. 2024; 14(1):31282.

PMID: 39732812 PMC: 11682433. DOI: 10.1038/s41598-024-82735-7.


Deciphering three predominant biopsy-proven phenotypes of IgG4-associated kidney disease: a retrospective study.

Luo S, Guo L, Yang Z, Shen R, Zhang T, Wang M Clin Kidney J. 2024; 17(5):sfae111.

PMID: 38783966 PMC: 11114465. DOI: 10.1093/ckj/sfae111.


Young Female With Hypereosinophilia, Rash, and Gait Disturbance: A Case Report.

Hariharan P, Nemchenok L, Hadi M, Williams V, Caliendo A Cureus. 2024; 16(3):e56498.

PMID: 38638789 PMC: 11026124. DOI: 10.7759/cureus.56498.


Renal involvement in eosinophilic granulomatosis with polyangiitis.

Reggiani F, LImperio V, Calatroni M, Pagni F, Sinico R Front Med (Lausanne). 2023; 10:1244651.

PMID: 37790127 PMC: 10544898. DOI: 10.3389/fmed.2023.1244651.