High occurrence of in vitro apoptosis of lymphocytes induced by serum from systemic lupus erythematosus patients is associated with increased serum levels of anti-C1q autoantibodies

Background The ethiopathogenesis of increased apoptosis of lymphocytes in systemic lupus erythematosus (SLE) is still incompletely understood but anti‐C1q autoantibodies have been shown to induce apoptosis in lymphocytes from healthy donors and certain cell lines. Aim This study was undertaken to in...

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Veröffentlicht in:International journal of rheumatic diseases 2013-08, Vol.16 (4), p.430-436
Hauptverfasser: Hasan, Siti Idayu, Mohd Ashari, Noor Suryani, Mohd Daud, Kamaliah, Che Husin, Che Maraina
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Sprache:eng
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Zusammenfassung:Background The ethiopathogenesis of increased apoptosis of lymphocytes in systemic lupus erythematosus (SLE) is still incompletely understood but anti‐C1q autoantibodies have been shown to induce apoptosis in lymphocytes from healthy donors and certain cell lines. Aim This study was undertaken to investigate the relationship between peripheral lymphocyte apoptosis and serum levels of anti‐C1q autoantibodies in SLE patients. Methods The sera of 124 patients with SLE involving 62 active SLE and 62 inactive SLE, fulfilling America College of Rheumatology (ACR) classification criteria for SLE (1997) were incubated with peripheral blood lymphocytes of healthy donors. The results were compared with 124 sex‐ and age‐matched normal controls. Apoptotic lymphocytes (AL) were detected by flow cytometry using annexin V and propidium iodide binding. Anti‐C1q autoantibodies were detected by an enzyme‐linked immunoassay kit for all SLE patients. Results Results demonstrated that the percentage of AL in the peripheral blood of active SLE patients was significantly higher (n = 62, 34.95 ± 12.78%) than that of the inactive SLE patients (n = 62, 30.69 ± 10.13%, P = 0.042, 95%CI = 0.16–8.36) and normal controls (n = 124, 27.92 ± 10.22%, P = 0.001, 95%CI = 3.33–10.73). The percentage of AL significantly correlated with serum levels of anti‐C1q autoantibodies in the active SLE patients (r = 0.263, P = 0.039) but not in the inactive SLE patients (r = 0.170, P = 0.185). Conclusion The results of this study suggest that increased serum levels of anti‐C1q autoantibodies are responsible for apoptosis and may play a pathogenic role in SLE patients, especially in active disease.
ISSN:1756-1841
1756-185X
DOI:10.1111/1756-185X.12062