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Arthritis Res. 2001; 3(Suppl A): P115.
Published online 2001 January 26. doi:  10.1186/ar284
PMCID: PMC3273286

Anti-Fcgamma receptor (FcgammaR) autoantibodies (Ab) delay apoptosis of polymorphonuclear cells (PMN) in systemic autoimmune diseases by inducing the production of G-CSF and GM-CSF

FcγRIIIb is expressed by PMN, and cell-free receptor has also been found circulating in body fluids. We have examined 222 patients with rheumatoid arthritis (RA), systemic lupus erythematosus and primary Sjögren's syndrome and classified anti-FcγR auto-Ab into three groups, based on the results of an indirect immunofluorescence (IIF) test and an ELISA : IIF+/ELISA+ (group A), IIF+/ELISA-(group B) and IIF-/ELISA+ (group C). PMN-binding Ab, i.e. groups A and B, prolonged the survival of PMN by delaying spontaneous apoptosis, and reduced adhesiveness and respiratory burst of these cells. Interestingly, recombinant non-glycosylated and purified glycosylated FcγR produced similar effects as the related auto-Ab.

To delineate the mechanism(s) by which the PMN life span is prolonged, we studied the response of PMN to F(ab')2 fragments of anti-FcγR (CD16) monoclonal Ab. CD16 engagement decreased apoptosis and prevented the up-regulation of β2 integrins, particularly CD11b which is the α chain of complement receptor 3, and CD18 which is its β chain.

The expression of mRNA for G-CSF and GM-CSF was induced. Release of these chimiokines followed CD16 stimulation, suggesting an autocrine involvement of survival factors in the rescue of PMN. The levels of G-CSF and GM-CSF paralleled the amounts of CD16 monoclonal Ab used to stimulate the cells. This set off a partial reduction of caspase 3 activity and was associated with down-expression of Bax. It was shown that anti-G-CSF and anti-GM-CSF Ab inhibited these events, while anti-TNFα was ineffective.

Overall, apoptosis of aged PMN can be modulated by signalling through FcγR, which may occur in patients with PMN-binding auto-Ab. This might be particularly relevant in the synovial fluid of patients with RA.


Articles from Arthritis Research are provided here courtesy of BioMed Central