慢性HBsAg携带者HBV-DNA的筛选。

Microbiologica Pub Date : 1991-10-01
F Bevilacqua, A Conti, A Marcello, G Angelini, D Di Piramo, M Rassu, L Dolci, L Piacentini, G Palù
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引用次数: 0

摘要

采用聚合酶链反应(PCR)和液相杂交(LPH)技术检测了52例慢性乙型肝炎表面抗原(HBsAg)携带者血清中HBV-DNA的存在。样本来自两组患者:A组包括34名慢性HBsAg携带者(“健康”个体),无肝细胞溶解或病毒复制;B组包括18例慢性HBsAg携带者,伴有肝细胞溶解(ALT水平至少为正常值的两倍)和激活的病毒复制标记物。A组PCR检测结果优于LPH,分别为7/34和5/34。在B组中,两种方法的敏感性没有差异,因为9/18的样本都是阳性的。这些数据强调了采用PCR技术筛选HBeAg-/HBsAg+-携带者的HBV-DNA的必要性。
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Screening of HBV-DNA in chronic HBsAg carriers.

A series of 52 serum samples from chronic HBsAg carriers was tested for the presence of HBV-DNA by means of the Polymerase Chain Reaction (PCR) and Liquid Phase Hybridization (LPH). The samples were obtained from two groups of patients: group A included 34 chronic HBsAg carriers ("healthy" individuals) without hepatocytolysis or viral replication; group B included 18 chronic HBsAg carriers with signs of hepatocytolysis (ALT levels at least twice the normal value) and activated markers of viral replication. PCR was superior to LPH in group A, with 7/34 versus 5/34 positive samples being detected, respectively. No difference in sensitivity was found between the two techniques in group B, since 9/18 samples were positive both cases. The data stress the need to adopt PCR for the HBV-DNA screening of HBeAg-/HBsAg+-carriers.

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