Immune complexes from SLE sera induce IL10 production from normal peripheral blood mononuclear cells by an FcγRII dependent mechanism: implications for a possible vicious cycle maintaining B cell hyperactivity in SLE. Issue 1 (1st January 2003)

• Record Type: Journal Article
• Authors: Rönnelid, J; Tejde, A; Mathsson, L; Nilsson-Ekdahl, K; Nilsson, B
• Is Part Of: Annals of the rheumatic diseases. Volume 62:Issue 1(2003)
• Page Start: 37
• Page End: 42
• Publication Date: 2003-01-01
• Subjects: systemic lupus erythematosus -- immune complexes -- interleukin 10 -- FcγRII; ELISA, enzyme linked immunosorbent assay -- ELISPOT, enzyme linked immunospot -- FcγR, Fc gamma receptor -- FCS, fetal calf serum -- HAGG, heat aggregated immunoglobulins -- IC, immune complex -- IFN, interferon -- IL, interleukin -- PBMC, peripheral blood mononuclear cells -- PBS, phosphate buffered saline -- PEG, polyethylene glycol -- SFC, spot forming cells -- SLE, systemic lupus erythematosus; Rheumatism -- Periodicals; 616.723005
• DOI: 10.1136/ard.62.1.37
• Languages: English
• ISSNs: 0003-4967

Abstract

Abstract : Background: Raised interleukin (IL)6 and IL10 levels are thought to contribute to the pathogenesis of systemic lupus erythematosus (SLE) by enhancing autoantibody production and immune complex (IC) formation. These immune complexes can then stimulate cellular reactions through Fc and complement receptors. Objective: To investigate whether circulating SLE ICs stimulate type 2 cytokine production. Methods: Twenty serum samples from patients with active SLE were compared with sera from 18 healthy controls. Sera and polyethylene glycol (PEG) precipitates from sera were added to peripheral blood mononuclear cell (PBMC) cultures, and the production of IL10 and IL6 was investigated by enzyme linked immunospot assay (ELISPOT) and enzyme linked immunosorbent assay (ELISA). Fc gamma receptor (FcγR) antibodies were used in blocking experiments, and flow cytometry was used to assess the correlation between monocyte FcγR expression and IC-induced cytokine production. Results: Ten per cent dilutions of the SLE sera induced a significantly increased number of IL10-producing cells in comparison with control sera (median, 11.75 v 1.25 spot forming cells/50 000 PBMC; p<0.0001). PEG precipitates from SLE sera also induced significantly increased levels of IL10 (p=0.016) and IL6 (p=0.042) in comparison with control PEG precipitates. IL10 production induced by SLE PEG precipitates or by artificial ICs could be blocked by anti-FcγRII antibodies, and the FcγRII expression on CD14+ monocytes correlated with the IC-induced production of IL10 and IL6. Conclusions: SLE sera stimulate IL10 and IL6 production from PBMC, and this effect is at least partly explained by precipitable ICs acting through FcγRII. This effect provides a possible mechanism for the enhanced production of IL10 in SLE, whereby B cell activation, antibody production, IC stimulated monocytes/macrophages, and type 2 cytokines create a vicious cycle that may help to maintain B cell hyperactivity in SLE.