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作 者:叶贤林[1] 朱为刚[1] 王良华[1] 尚桂芳[1]
机构地区:[1]深圳血液中心,广东深圳518035
出 处:《中华医院感染学杂志》2006年第8期874-876,共3页Chinese Journal of Nosocomiology
基 金:瑞士罗氏分子诊断公司合作资助项目
摘 要:目的了解和分析HBsAg阴性无偿献血者乙型肝炎感染状况。方法应用罗氏聚合酶链反应(PCR)定量检测方法追踪6位HBsAg阴性,DNA阳性感染者的病毒载量,同时对进行基因分型、血清转换及ALT等多项指标的的动态追踪分析观察。结果6例阳性样本经过至少40d追踪发现,3例发生了血清转换现象;DNA定量追踪分析表明,病毒载量在(35~1.8)×10^4拷贝/ml之间,1例为急性乙型肝炎感染,病毒载量峰值为1.8×10^4拷贝/ml,3例呈低水平携带状态,病毒载量在100~500拷贝/ml之间波动;1例病毒载量下降至检不出,而HBsAg转换成阳性;最后1例间或能检出病毒,载量〈100拷贝/ml。结论本实验结果认为有必要进行献血者HBV核酸筛查工作,进一步提高输血安全性。OBJECTIVE To investigate and analyze the kinetics of serological marks and virus load of the follow-up blood donors. METHODS The quantitation of HBV DNA of 6 HBsAg negative and DNA positive blood donors was detected by Roche PCR Monitor,and the donors were genotyped and traced by serological tests. RESULTS Three of 6 follow-up donor samples were seroconverted after more than 40 days follow-up study. The viral loads were with range of (35-1.8) × 10^4 copies/ml, 1 of 6 donors had acute infection, the peak load was 1.8 ×10^4 copies/ml, 3 of 6 were with lower level HBV carrier with fluctuating viral load ranged 100-500 copies/ ml. One donor had decreasing viral load,when HBsAg converted to positive,virus wasn't detected. The last one had fluctuating virus load below 100 copies/ml, intermittently falling below the threshold of the assay. CONCLUSIONS It is necessary to implement HBV DNA detection for blood screening, and further strengthen the Safety of blood transfusion.
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