摘要
目的探讨糖皮质激素(简称激素)治疗对系统性红斑狼疮(SLE)患者外周血CD4^+CD25^+T细胞(调节性T细胞)亚群CD62L表达的影响。方法采用流式细胞仪检测了10例初发未经治疗的SLE患者和25例经激素治疗后的SLE患者外周血CD4^+CD25^+T细胞亚群CD62L的表达,并与12例正常人对照组相比较。结果未经治疗的初发SLE患者CD62L^+和CD62L^-的CD4^+CD25^+T细胞均较健康对照组明显减少。激素治疗后,SLE患者外周血CD4^+CD25^+CD62L^+T细胞显著升高,而且与糖皮质激素剂量有关。大剂量激素治疗组CD4^+CD25^+CD62L^+T细胞显著高于未治疗组和正常人对照组,但小剂量激素治疗组CD4^+CD25^+CD62L^+T细胞仅高于未治疗组。然而无论小剂量激素治疗组还是大剂量激素治疗组的CD4^+CD25^+CD62L^-T细胞与正常人对照组比较差异均无统计学意义。SLE患者外周血CD4^+CD25^+CD62L^+ T细胞与疾病活动指数成负相关。结论糖皮质激素可能上调SLE患者外周血CD4^+CD25^+CD62L^+T细胞的生成.促进外周免疫耐受,从而缓解病情。
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 significantly 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^+ CD25^+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.
出处
《中华皮肤科杂志》
CAS
CSCD
北大核心
2007年第6期362-364,共3页
Chinese Journal of Dermatology
基金
广东省科技计划基金(2004B31201004)