Our aims were to determine the prevalence of neutrophil antibodies in patients with primary Sjogren's syndrome (pSS), identify their target antigen(s), and evaluate their functional significance. Neutrophil antibodies were detected using an indirect immunofluorescence (IIIF) test and an enzyme-linked immunosorbent assay (ELISA), using recombinant human Fc-gamma receptor (Fc gamma RIIIb) as a capture agent. Luminol-dependent chemiluminescence was then measured by an established technique. Antibodies to neutrophils were detected in 30 of 66 patients (45%) and categorized on the basis of positivity for the two assays: IIF+/ELISA+ (group A: five patients), IIF+/ELISA- (group B: five patients), and IFF-/ELISA+ (group C: 20 patients). All positive sera contained antibodies directed to the neutrophil specific Fc gamma RIIIb, and none of them bound to NAnull neutrophils. The titer of neutrophil-reactive antibodies (groups A and B) showed no correlation with the neutrophil count, but these autoantibodies did reduce the cell ability to generate a respiratory burst. Thus, neutrophil antibodies are common in patients with pSS. Their main target appears to be Fc gamma RIII, and this may partly account for the dysfunction in Fc gamma R-mediated clearance by the reticuloendothelial system reported in these patients.
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ARTICLES|
November 1, 1995
Heterogeneity of neutrophil antibodies in patients with primary Sjogren's syndrome
A Lamour,
A Lamour
Laboratory of Immunology, Brest University Medical School, France.
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R Le Corre,
R Le Corre
Laboratory of Immunology, Brest University Medical School, France.
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YL Pennec,
YL Pennec
Laboratory of Immunology, Brest University Medical School, France.
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J Cartron,
J Cartron
Laboratory of Immunology, Brest University Medical School, France.
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P Youinou
P Youinou
Laboratory of Immunology, Brest University Medical School, France.
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Blood (1995) 86 (9): 3553–3559.
Citation
A Lamour, R Le Corre, YL Pennec, J Cartron, P Youinou; Heterogeneity of neutrophil antibodies in patients with primary Sjogren's syndrome. Blood 1995; 86 (9): 3553–3559. doi: https://doi.org/10.1182/blood.V86.9.3553.bloodjournal8693553
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November 1 1995
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