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机构地区:[1]兰州大学第一医院感染病科,甘肃兰州730000
出 处:《第四军医大学学报》2009年第15期1422-1424,共3页Journal of the Fourth Military Medical University
摘 要:目的:研究TLR7在慢性乙型肝炎患者外周血单核细胞的表达及其与IL-12,HBV-DNA载量之间的关系,探讨TLR7在抗病毒免疫应答中的作用机制及意义.方法:用实时荧光定量PCR法检测38例具有不同HBV-DNA载量的慢性乙型肝炎患者和12例正常对照者外周血单核细胞TLR7mR-NA表达,患者按病毒载量分为低、中、高3组.实时荧光定量PCR法测定血清病毒载量,ELISA法测定血清IL-12的水平,多组均数间的比较用方差分析,直线相关性分析用Spearman秩相关.结果:患者组中TLR7mRNA水平比正常对照组显著降低(P<0.01),3组患者间TLR7mRNA表达有显著差异且与血清HBV-DNA载量呈负相关,患者组血清IL-12比正常人显著增高,3组患者外周血清IL-12,低、中病毒载量组的差异无统计学意义(P>0.05),其余各组间差异有统计学意义(P<0.01),且与病毒载量呈负相关(r=-0.075,P<0.01).结论:TLR7在慢性乙型肝炎患者外周血单核细胞的表达下降,TLR7与IL-12可能在慢性乙型肝炎中对病毒清除有重要作用,其水平降低可能与疾病的慢性化机制有关.AIM: To investigate the correlation between the expression of TLR7 mRNA in peripheral blood monouclear cells (PBMCs) of chronic hepatitis B patients and IL-12 and HBVDNA load and to explore the role of TLR7 in anti-HBV-DNA. METHODS: TLR7 mRNA expression was examined by real-time quantitative PCR in 38 patients with different HBV-DNA loads and 12 healthy controls, and the patients were divided into 3 groups based on low, medium or high viral load. HBV-DNA was examined by real-time quantitative PCR and the level of serum interleukin-12( IL-12 ) was examined by ELISA. The difference of mean between groups was studied by variance analysis and the correlation between HBV-DNA load and TLR7 expression was analyzed by Spearman rank correlation. RESULTS: The results demonstrated that the expression of TLR7 was significantly lower in HBV infection groups than that in control groups, with statistically significant difference ( P 〈 0. 01 ). There was statistical difference in TLR7 mRNA expression among the 3 groups of chronic hepatitis B patients, and the expression of TLR7 was negatively correlated with HBVDNA load. The level of serum IL- 12 was significantly higher in HBV infection groups than that in controls. There was no statistical difference between the groups of low and medium virus load ( P 〉 0.05 ), while the difference in the difference was statistically significant between other groups (P 〈 0.01 ). IL-12 was negatively correlated with HBV-DNA load (r = - 0. 075, P 〈 0. 01 ). CONCLUSION: TLR7 mRNA expression is down-regulated in PBMCs of HBV-infected patients. Both TLR7 and IL-12 play some important roles in clearing out virus and the down-regulation of them may relate to the chronic mechanism of hepatitis B.
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