首页> 外文期刊>European journal of internal medicine >Determination of hepatitis B virus DNA incidence, viral load, and mutations in blood donors with HBsAg and anti-HBs-negative serology and antibodies to hepatitis B core antigen.
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Determination of hepatitis B virus DNA incidence, viral load, and mutations in blood donors with HBsAg and anti-HBs-negative serology and antibodies to hepatitis B core antigen.

机译:使用HBsAg和抗HBs阴性血清学以及抗乙型肝炎核心抗原抗体的献血者确定乙型肝炎病毒DNA的发生率,病毒载量和突变。

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BACKGROUND: The aim of the present study was to determine hepatitis B virus DNA incidence, viral load, and mutations in blood donors with HBsAG and anti-HBs negative serology and antibodies to hepatitis B core antigen. METHODS: Blood samples were collected from 1000 blood donors with HBsAg-negative test results. Anti-HBc total screening was performed using the ELISA method. HBsAg-negative/anti-HBc total-positive samples were tested for anti-HBs, anti-HBc IgM, HBeAg, and anti-HBe. Samples with isolated anti-HBc were determined for viral load of HBV DNA using real-time PCR. RESULTS: Anti-HBc total was established as positive in 200 (20%) of the 1000 blood donors. While anti-HBs was negative in 59 (29.5%) of the 200 anti-HBc-positive samples, it was found to be positive in 141 (70.5%) of them. All of the other hepatitis B markers were negative in all of the anti-HBs-negative samples. HBV DNA was not detected in the sera of the isolated anti-HBc-positive blood donors with real-time PCR. CONCLUSION: Although we could not detect HBV DNA in the sera of the isolated anti-HBc-positive blood donors, findings in the literature suggest that anti-HBc testing should be used in combination with HBsAg for the screening of blood donors to reduce risk. After that, the most appropriate algorithm to follow can be HBV DNA screening of donors.
机译:背景:本研究的目的是确定乙型肝炎病毒DNA的发生率,病毒载量以及HBsAG和抗HBs阴性血清学以及乙型肝炎核心抗原抗体的献血者中的突变。方法:从1000名献血者中采集血样,HBsAg阴性。使用ELISA方法进行抗HBc总筛选。测试了HBsAg阴性/抗HBc总阳性样品的抗HBs,抗HBc IgM,HBeAg和抗HBe。使用实时PCR测定分离出的抗HBc样品的HBV DNA病毒载量。结果:1000名献血者中有200名(20%)的抗HBc总阳性。虽然200份抗HBc阳性样本中有59份(29.5%)的抗HBs阴性,但其中141份(70.5%)却呈阳性。在所有抗HBs阴性样品中,所有其他乙型肝炎标志物均为阴性。实时PCR未在分离的抗-HBc阳性献血者血清中检测到HBV DNA。结论:尽管我们无法在分离的抗HBc阳性献血者的血清中检测到HBV DNA,但文献发现建议应将抗HBc检测与HBsAg结合使用以筛查献血者以降低风险。之后,最合适的算法可以是对供体的HBV DNA筛选。

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