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作 者:张濛[1] 孟洋[2] 甘雨舟 赵晓珍 王燕[2] 孙晓麟[3] 张学武[3] Zhang Meng Meng Yang Gan Yuzhou Zhao Xiaozhen Wang Yan Sun Xiaolin Zhang Xuewu(Department of Nephropathy Rheumatology, Nanyang Central Hospital, Affiliated to Zhengzhou University, Henan 473009, Chin)
机构地区:[1]郑州大学附属南阳市中心医院肾病风湿免疫科,473009 [2]郑州大学第五附属医院风湿免疫科 [3]北京大学人民医院风湿免疫科
出 处:《中华风湿病学杂志》2017年第9期601-604,共4页Chinese Journal of Rheumatology
基 金:国家自然科学基金(81471601);北京市自然科学基金(7152150);河南省教育厅重点科技攻关项目(14A320053)
摘 要:目的探讨血小板反应蛋白-1(TSP-1)在SLE的临床意义,及其可能在SLE发生发展中发挥的作用。方法SLE患者138例(女性124例,男性14例),健康对照组60名,运用ELISA法检测2组血清中TSP-1表达水平,运用Spearman相关分析,分析TSP-1蛋白表达量与SLE患者补体C3、补体C4、抗dsDNA抗体、RF和SLEDAI等指标的相关性。结果健康对照组血清中TSP-1的含量(102 348±39 827)ng/ml明显高于SLE患者组(15 276±7 183)ng/ml,TSP-1与补体C3(r=0.386,P〈0.01)和补体C4(r=0.301,P〈0.01)等实验室指标呈正相关,而与SLE患者血清中抗dsDNA抗体(r=-0.221,P=0.009)、RF(r=-0.186,P=0.029)、SLEDAI(r=-0.273,P=0.001)呈负相关。结论TSP-1可能在SLE疾病过程中发挥免疫负调节功能,抑制自身免疫炎症的发展和自身抗体的产生,可能成为SLE治疗的新手段。ObjectiveTo evaluate the clinical significance of serum thrombospondin-1 (TSP-1) in systemic lupus erythematosus (SLE), and explore its possible involvement in SLE pathogenesis.MethodsOne hundred and thirty-eight patients diagnosed with SLE, including 124 cases of females and 14 males, as well as 60 healthy controls were recruited into this study. Enzyme-linked immunosorbent assay (ELISA) was used to determine serum TSP-1 expression level between the two groups. Spearman correlation analysis method was used to analyze the correlation between TSP-1 level of complement 3, complement 4, anti-double-stranded DNA, Rheumatoid factor and systemic lupus erythematosus disease activity index (SLEDAI).ResultsTSP-1 level in healthy control group was much higher than that in SLE patients. TSP-1 serum levels in SLE patients was positively correlated with complement 3 (r=0.386, P〈0.01), complement 4 (r=0.301, P〈0.01), and negatively correlated with anti-double-stranded DNA (r=-0.221, P=0.009), RF (r=-0.186, P=0.029) and SLEDAI (r=-0.273, P=0.001).ConclusionTSP-1 may play an immune-regulatory role in the development of SLE by inhibiting inflammation and autoantibody production. It could become a potential therapeutic target for the treatment of SLE.
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