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作 者:范兴忠[1] 李宏[1] 刘文峰[2] 赵建强[1]
机构地区:[1]山东省潍坊市人民医院肾内科,261041 [2]山东寿光潍坊医学院附属寿光医院,262700
出 处:《免疫学杂志》2010年第1期56-57,62,共3页Immunological Journal
摘 要:目的通过观察肾病综合征(NS)免疫治疗前后白细胞介素-4(interleukin-4,IL-4)和IL-10水平的变化,探讨其临床意义。方法以ELISA检测52例NS患者在接受强的松和环磷酰胺治疗前及4周后血清IL-4和IL-10水平。结果NS患者血清IL-4水平显著增高(P<0.01),并与血清β_2微球蛋白呈显著正相关(n=52,r=0.352.P<0.05),血清IL-10水平与健康人无显著差异。治疗4周后血清IL-4和IL-10水平显著降低(P<0.05),尿蛋白排出量显著低于治疗前(P<0.05)。结论IL-4、IL-10参与了NS发病过程,强的松和环磷酰胺可通过调节IL-4和IL-10产生而调节NS的免疫紊乱,NS的免疫治疗方案可根据细胞因子水平(包括抗炎细胞因子IL-4和IL-10)调整。To investigate the roles of interleukin-4(IL-4) and interleukin-10(IL-10)in pathogenesis of nephrotic syndrome(NS)and its clinical significance.Serum levels of IL-4 and IL-10 in 52 patients with NS were determined by ELISA at pre-treatment and 4 weeks after treatment with prednisone and cyclophosphamide.Serum level of IL-4 in NS patients was significant higher than those in healthy controls(P 0.01),and there was a positive correlation between serum IL-4 level and serumβ_2-MG(n=52,r=0.352,P0.05),while no significant difference of serum IL-10 levels was found between NS group and healthy controls.At 4 weeks after treated with prednisone and cyclophosphamide, the serum levels of IL-4 and IL-10 as well as the 24-hour urinary protein excretion were significant lower than those in pre-treated NS patients(P0.05).The results imply that IL-4 and IL- 10 may take part in immune pathogenesis of NS,while prednisone and cyclophosphamide may have a significant inhibiting effect on the production of IL-4 and IL-10 in NS,thus the immunotherapy of NS may he adjusted according to the immune activity of disease(including anti-inflammatory immune-regulating cytokines IL-4 and IL-10).
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