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作 者:洪丰[1,2,3,4] 白守国[1,2,3,4] 赵洪涛 孙文生[1,2,3,4]
机构地区:[1]山东省济宁市第一人民医院 [2]山东省济宁市妇女儿童医院 [3]山东省立医院 [4]山东医科大学
出 处:《胃肠病学和肝病学杂志》1998年第2期120-122,共3页Chinese Journal of Gastroenterology and Hepatology
摘 要:目的和方法:经肝活检诊断为慢性迁延性肝炎(CPH)51例,均做PCR、斑点杂交进行肝组织、血清HBVDNA检测,同时用ELISA方法检测了HBV血清标志物。结果,HBVDNA检出率依次为肝组织PCR941%(48/51)、血清PCR922%(47/51)和肝组织斑点杂交902%(46/51)。三者之间无显著差异(χ2=0495,P>005)。各项血清标志物总检出率HBsAg372%(19/51),HBeAg333%(17/51)和抗-HBe215%(11/15),显著低于PCR和斑点杂交HBVDNA的检出率(χ2=30.9,P<0005)。在抗-HBe(+)的11例患者中10例检出肝组织和血清HBVDNA,8例抗-HBs(+)患者,6例肝组织及血清PCRHBVDNA阳性,结论:表明抗-HBe(+)及/或抗-HBs(+)不能代表HBV复制停止或被清除。Abstract Aim and Methods:We used polymerase chain reaction(PCR) assay and slot-blot hybridization for detecting hepatitis B Virus (HBV) DNA in the serum and hepatic tissue of 51 patients with chronic persistent hepatitis(CPH) diagnosed by hepatic biopsy, while using ELISA to detect HBV five seral items. Results: The results showed that:of 94.1%(48/51) cases positive for HBV DNA by PCR of hepatic tissue, 92.2%(47/51) Cases positive for HBV DNA by PCR of serum and 90.2%(46/51) by slot-blot hybridization of hepatic tissue. No Significant differenciation among them (χ 2=0.495,P>0 05). the positive rates of HBV five seral items as follows:HBsAg 37.2%(19/51),HBeAg 33.3%(17/51) and antibody against HBV e antigen 21.5%(11/51), Significantly lower than the positive rate of HBV DNA by PCR and slot-bolt hybridization (χ 2=30.9,P<0 005). In 11 patients for antibody against HBV e antigen, 10 were positive for HBV DNA by PCR of serum and hepatic tissue, while in 8 patients positive for antibody against HBV surface antigen, 6 were positive. Conclusions: this indicated that positive for antibody against HBV e antigen and/or for antibody against HBV surface antigen couldn′t tell the cancelation or stop of replication of HBV, the hepatic disorder might still exist.
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