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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Increased neutrophil oxidative burst metabolism in systemic lupus erythematosus

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Author(s):
Perazzio, S. F. [1] ; Salomao, R. [2] ; Silva, N. P. [1] ; Andrade, L. E. C. [1, 3]
Total Authors: 4
Affiliation:
[1] UNIFESP EPM, Div Rheumatol, Sao Paulo - Brazil
[2] UNIFESP EPM, Div Infect Dis, Immunol & Virol Lab, Sao Paulo - Brazil
[3] Fleury Med & Hlth Labs, Sao Paulo - Brazil
Total Affiliations: 3
Document type: Journal article
Source: Lupus; v. 21, n. 14, p. 1543-1551, DEC 2012.
Web of Science Citations: 13
Abstract

Introduction: There is increased frequency of discoid lesions (2.7%) and SLE (0.5%) in patients with chronic granulomatosus disease, but the literature is still controversial about phagocyte oxidative burst in SLE patients. Materials and methods: 300 SLE patients and 301 blood donors were evaluated for quantitation of the oxidative burst in phagocytes by flow cytometry based on the oxidation of 2,7-dichlorofluorescein-diacetate after stimuli with Staphylococcus aureus and Pseudomonas aeruginosa. Results: Neutrophils from SLE patients displayed higher basal reactive oxygen species (ROS) production than healthy controls {[}Mean of fluorescence intensity (MFI)=53.77 +/- 11.38 vs 15.08 +/- 2.63, p<0.001] and after stimulation with S. aureus (MFI=355.46 +/- 58.55 vs 151.92 +/- 28.25, p<0.001) or P. aeruginosa (MFI=82.53 +/- 10.1 vs 48.99 +/- 6.74, p<0.001). There was stronger neutrophil response after bacterial stimuli (Delta MFI) in SLE patients than in healthy controls (S. aureus=301.69 +/- 54.42 vs 118.38 +/- 26.03, p<0.001; P. aeruginosa=28.76 +/- 12.3 vs 15.45 +/- 5.15, p<0.001), but no difference with respect to the oxidative burst profile according to disease activity (SLEDAI >= 6) or severity (SLICC-DI >= 2). Patients with kidney involvement presented higher basal and stimulated ROS production in neutrophils. Discussion: The present findings corroborate the important role of innate immunity in SLE and implicate neutrophils in the pathophysiology of the disease. Lupus (2012) 21, 1543-1551. (AU)