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Superoxide release in juvenile systemic lupus erythematosus
Authors:Roberto Marini  Antonio Condino-Neto  Simone Appenzeller  André M. Morcillo  Lilian T. L. Costallat
Affiliation:1. Department of Pediatrics and Medicine-Rheumatology Unit, Faculty of Medical Science, State University of Campinas, Campinas, Brazil
2. Center for Investigation in Pediatrics, Department of Pediatics and Medicine-Rheumatology Unit, Faculty of Medical Science, State University of Campinas, Campinas, Brazil
3. Rheumatology Division, Department of Medicine, Faculty of Medical Science, State University of Campinas, 13087-500, Campinas, Brazil
Abstract:The objective of this study was to analyze the un-stimulated and stimulated release of superoxide anion (O2 ?) by granulocytes and monocytes in juvenile systemic lupus erythematosus (jSLE). The un-stimulated and phorbol myristate acetate (PMA, 30 nM)-induced O2 ?by granulocytes and monocytes were determined in six different times of incubation in patients with 23 jSLE and 28 controls. The analysis compared the jSLE group, which was classified into two subgroups by SLEDAI in one inactive subgroup (score <3) (n?=?13 patients) and one active subgroup (score ≥3) (n?=?10 patients) to the same control group. At time of blood withdrawal, 13 (56.52%) had inactive and 10 (43.47%) patients had active SLE. jSLE patients’ granulocytes and monocytes had always a lower un-stimulated O2 ? production when compared to controls. Stimulated granulocytes had an increased O2 ? production at baseline followed by a significant lower production at 60?min in jSLE when compared to controls. Stimulated monocytes had a similar O2 ? production among patients with jSLE and controls. The results suggest a defect in phagocytic function in jSLE. The significant higher release of O2 ? in the assays of the stimulated granulocytes, in the initial instances, the so-called respiratory burst, could be attributed to the inflammatory state of phagocytes.
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