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作 者:马艳丽[1] 任万华[1] 董振芳[1] 主余华[1]
机构地区:[1]山东大学山东省立医院肝病中心,济南250021
出 处:《胃肠病学和肝病学杂志》2005年第6期584-586,共3页Chinese Journal of Gastroenterology and Hepatology
摘 要:目的探讨慢性乙型肝炎(CHB)肝组织HBVcccDNA定量与乙型肝炎的关系。方法分别采用荧光定量PCR、酶联免疫吸附分析法(ELISA)检测48例CHB肝组织HBV cccDNA定量、肝组织和血清HBV DNA定量、乙型肝炎病毒标志物。同时用链霉菌抗生素蛋白-过氧化物酶连接法(SP)检测肝细胞中HBcAg表达。分析肝组织HBV cccDNA与组织和血清HBV DNA、HBeAg、肝细胞内HBcAg水平及肝脏炎症活动度的关系。结果1.肝组织HBV cccDNA定量与组织和血清HBV DNA定量呈正相关(r=0.837,P<0.001;r=0.627,P<0.005);2.肝组织HBV cccDNA定量与肝细胞内HBcAg半定量呈正相关(r=0.618,P<0.005);3.肝组织HBV cccDNA定量与肝脏炎症活动度无明显相关(P>0.05):4.HBeAg阳性较抗-HBe阳性患者肝组织HBV cccDNA定量、肝组织和血清HBV DNA定量高(P<0.05)。结论荧光定量PCR法检测肝组织HBV cccDNA定量是评价HBV复制最直接可靠的指标,在CHB的诊断和抗病毒治疗中有重要意义。但与肝组织炎症无明显相关。Objective To study the and chronic hepatitis B (CHB). Methods clinical and pathological relationship Quantitative PCR were used to detect between the quantitation of HBV cccDNA HBV cccDNA in liver biopsies. The same method was used to examine HBV DNA in sera and liver biopsies. ELISA(Enzyme-Linked Immunosorbent Assay) was used to detect hepatitis B serum markers. Expression of HBcAg in liver tissue was detected by using SP method. Results 1 .There was a strong correlation between the cccDNA levels in the biopsy samples and HBV DNA levels in the sera and liver biopsies. 2. There was a significant correlation between cccDNA copy number and the number of HBcAg + cells in liver tissue. 3. The correlation between quantitation of eccDNA in liver biopsies and histological activity index was not found.4. HBeAg-positive patients had higher HBV cccDNA in liver tissue,and HBV DNA in serum and liver tissue compared with anti-HBe-positive patients. Conclusion Quantitation of HBV cecDNA by real - time fluorescence PCR is a sensitive, stable, and reliable marker to assess HBV replication. And it plays a significant role in the diagnosis and treatment of CHB. But it has no obvious correlation with the liver inflammation.
分 类 号:R373.2[医药卫生—病原生物学]
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