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机构地区:[1]齐齐哈尔医学院附属第三医院检验科,黑龙江齐齐哈尔161000
出 处:《中华医院感染学杂志》2010年第4期502-503,共2页Chinese Journal of Nosocomiology
摘 要:目的探讨血清HBV-DNA水平与HBV血清标志物的相关性。方法采用实时荧光定量PCR对1517例HBV感染者血清标本中HBV-DNA含量进行检测,同时用ELISA法检测其HBV免疫标志物。结果HBsAg、HBeAg、HBcAb阳性组患者血清HBV-DNA检出率98.24%;HBsAg、HBeAg阳性组为100.00%;HBsAg、HBeAb、HBcAb阳性组为60.98%;HBsAg、HBcAb阳性组为37.71%;HBcAb阳性组为12.90%。结论患者血清HBV-DNA的阳性率与HBV血清标志物的存在状态相关,采用FQ PCR法检测HBV-DNA能更准确、直接地反映体内病毒复制情况。OBJECTIVE To investigate the relationship between the level of HBV-DNA and Serum markers. METHODS FQ PCR was used to detect the contents of serum HBV-DNA in 1517 patients infected HBV and ELISA was used to detect the immunological markers. RESULTS The detected rate of HBsAg(+), HBeAg(+), HBcAb(+) group were 98.24%, HBsAg(+), HBeAg(+) group 100.00% of HBsAg(+), HBeAb(+), HBcAb(+) group 60.98 %, of HBsAg(+), HBcAb(+) showed a HBV-DNA group 37.71%, and of HBcAb(+) showed a HBV-DNA group was 12.90%. CONCLUSIONS The positive rate of serum HBV-DNA is related to the mode of serum HBV markers. The result of serum HBV-DNA detected by FQ-PCR can reflect the replication of hepatitis B virus more correctly and directly.
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