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作 者:张文兰[1] 胡同平[1] 王慧[1] 庞春燕[1] 任艳玲[1] 赵剑波[1] 尹芳蕊[1] 王永福[1]
机构地区:[1]包头医学院第一附属医院中心实验室,014010
出 处:《免疫学杂志》2013年第6期510-513,共4页Immunological Journal
基 金:内蒙古自治区高等学校科学研究项目(NJZY12219)
摘 要:目的研究SLE组和健康对照组外周血单核细胞中TLR-4、IRAK-M的mRNA表达情况和血清中TNF-α、IL-6、IL-10水平。方法采用qRT-PCR技术,检测SLE组和健康对照组单核细胞中TLR-4、IRAK-M的mRNA表达量;同时采用ELISA方法检测血清中TNF-α、IL-6、IL-10水平;相关性分析采用Pearson或Spearman。结果活动期SLE组TLR-4的mRNA表达量明显高于稳定期SLE组和健康对照组(P<0.05);SLE组IRAK-M的mRNA表达量明显低于健康对照组(P<0.05),活动期SLE组IRAK-M的mRNA表达量明显低于稳定期SLE组(P<0.05);SLE组TNF-α、IL-6、IL-10水平均高于健康对照组(P<0.05),活动期SLE组TNF-α、IL-6、IL-10水平均高于稳定期SLE组(P<0.05);相关分析显示:TLR-4的mRNA表达量、TNF-α、IL-6、IL-10的表达水平均与SLEDAI评分呈正相关(P<0.05),而IRAK-M的mRNA表达量与SLEDAI评分呈负相关(P<0.05)。结论 TLR-4、IRAK-M在SLE的发病中有一定意义;临床可以通过对TLR-4、IRAK-M的mRNA表达量、TNF-α、IL-6、IL-10的表达水平的监测来作为判断SLE疾病活动和预后的指标。This study designed to compare the expression of TLR-4 and IRAK-M in monocytes and the levels of TNF-α、IL-6、IL-10 in serum between SLE patients and healthy controls. The qRT-PCR was performed formRNA measurement and ELISA was used for cytokine quantification. The Pearson or Spearman correlation between TLR-4, IRAK-M, TNF-α、IL-6、IL-10 and SLEDAI were computed to explore their roles in the pathogenesis ofSLE. The result showed that the mRNA expression of TLR-4 in active group was significantly higher than that of stable group and healthy controls (P 〈 0.05); the mRNA expression of IRAK-M in SLE patients was significantlylower than that of healthy controls (P〈 0.05); and the mRNA expression of IRAK-M in active group was significantly lower than that of stable group (P〈 0.05). The levels of TNF-α、IL-6 and IL-10 in serum of SLE patients weresignificantly higher than those of healthy controls (P〈 0.05); and the levels of TNF-α、IL-6 and IL-10 in active group were significantly higher than those of stable group (P〈 0.05). Correlation analysis showed that the levels of TLR-4, TNF-α, IL-6 and IL-10 were positively correlated with SLEDAI (P〈 0.05), but the mRNA expression of IRAK-M was negatively correlated with SLEDAI (P 〈 0.05). This study indicated that TLR-4 and IRAK-M playcertain roles in the pathogenesis of SLE. We can evaluate the SLE disease activity and prognosis by determining TLR-4, IRAK-M, TNF-α, IL-6 and IL-10.
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