Chinese Journal of Dermatology

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Glucocorticoids treatment upregulates the expression of CD62L in CD4+CD25+T cells in peripheral blood monocytes of patients with systemic lupus erythematosus

TAN Guo-zhen1, PENG Hui2, MAO Yue-ping1, ZENG Fan-qin1   

  1. Department of Dermatology, Second Affiliated Hospital of Zhongshan University, Guangzhou 510120, China
  • Received:2006-07-03 Online:2007-06-15 Published:2007-06-15

Abstract: Objective To investigate the effect of glucocorticoids(GC)treatment on the expression of CD62L in CD4+ CD25+ T cells in peripheral blood monocytes(PBMC)of patients with systemic lupus erythematosus(SLE).Methods Flow cytometry was used to detect the expression of CD62L in CD4+ CD25+ T cells in PBMC of 35 SLE patients(10 untreated,25 treated with GC)and 12 normal human controls.Results The frequencies of both CD4+CD25+ CD62L+ T cells and CD4+CD25+ CD62L- T cells were signifi-cantly decreased in untreated SLE patients compared with the controls[(4.12±3.68)% vs(9.27±4.44)%,P<0.05 and(1.15±0.99)% vs(4.25±2.21)%,P<0.05].The frequency of CD4+CD25+ CD62L+T cells in SLE patients treated with GC increased greatly;this increase was related to the dose of GC.The frequency of CD4+ CD25+ CD62L+T cells in SLE patients treated with high-dose GC was higher than that in untreated SLE patients and normal controls[(14.84±6.41)% vs(4.12±3.68)%,P<0.05 and(14.84±6.41)vs(9.27±4.44)%,P<0.05],while that in SLE patients treated with low-dose GC was only higher than that in untreated SLE patients[(9.07±5.27)% vs(4.12±3.68)%,P<0.05)]. No difference was found in the frequency of CD4+CD25+ CD62L-T cells between either SLE patients treated with high-dose GC or those with low-dose GC and the controls.The frequency of CD4+ CD25+CD62L+T cells had a negative correlation with disease activity of SLE(SLEDAI).Conclusion GC treatment can decrease the disease activity in SLE by upregulating the generation of CD4+CD25+ T cells,especially CD4+ CD25+ CD62L+T cells,hence promoting peripheral immunotolerance.

Key words: Lupus erythematosus, systemic, Glucocorticoids, T-lymphocytes