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核酸检测阴性的乙型肝炎病毒窗口期供体受者的乙型肝炎潜伏期延长。

Prolonged incubation period of hepatitis B in a recipient of a nucleic acid amplification test-negative hepatitis B virus window donation.

机构信息

Department of Blood Transfusion, Fujita Health University Hospital, Toyoake, Aichi, Japan.

Department of Molecular Laboratory Medicine, Fujita Health University School of Medical Sciences, Toyoake, Aichi, Japan.

出版信息

Transfusion. 2021 Sep;61(9):2782-2787. doi: 10.1111/trf.16557. Epub 2021 Jul 14.

Abstract

BACKGROUND

The occurrence of transfusion-transmitted hepatitis B virus (HBV) infection has fallen dramatically due to continuous improvements in pre-transfusion laboratory testing. However, the characteristics of transfusion-transmitted HBV infection caused by individual donor nucleic acid amplification test (ID-NAT)-negative blood products are unclear.

CASE PRESENTATION

A 76-year-old woman with acute myeloid leukemia was diagnosed with transfusion-transmitted HBV infection after receiving apheresis platelets derived from an ID-NAT-negative blood donation. This case was diagnosed definitively as transfusion-mediated because complete nucleotide homology of a 1556 bp region of the HBV Pol/preS1-preS2-S genes and a 23 bp region of the HBV core promoter/precore between the donor and recipient strains was confirmed by PCR-directed sequencing. The case is uncommon with respect to the unexpectedly prolonged HBV-DNA incubation period of nearly 5 months after transfusion (previously, the longest period observed since the recent implementation of ID-NAT pre-transfusion laboratory testing in Japan was 84 days). Slow-replicating HBV genotype A2 may contribute to the prolonged incubation period; also, the quantity of apheresis platelets delivered in a large volume of plasma, and/or the immune response of the recipient suffering from a hematological neoplasm, may have contributed to establishment of HBV infection in the recipient. This was supported by analysis of three previously documented cases of transfusion-transmitted HBV infection by blood products derived from ID-NAT-negative donations in Japan.

CONCLUSION

Continuous monitoring of HBV infection for longer periods (>3 months) may be required after transfusion of blood components from an ID-NAT-negative HBV window donation.

摘要

背景

由于输血前实验室检测的不断改进,输血传播乙型肝炎病毒(HBV)感染的发生率显著下降。然而,个体供者核酸扩增检测(ID-NAT)阴性血液制品引起的输血传播 HBV 感染的特征尚不清楚。

病例介绍

一名 76 岁女性,患有急性髓系白血病,在接受来自 ID-NAT 阴性献血的单采血小板输注后被诊断为输血传播 HBV 感染。该病例被明确诊断为输血介导的,因为通过 PCR 定向测序证实了供体和受者株之间 HBV Pol/preS1-preS2-S 基因的 1556bp 区域和 HBV 核心启动子/precore 区域的 23bp 区域的 HBV 完全核苷酸同源性。该病例较为罕见,因为输血后 HBV-DNA 的潜伏期长达近 5 个月(此前,自日本最近实施 ID-NAT 输血前实验室检测以来,观察到的最长潜伏期为 84 天)。慢复制 HBV A2 基因型可能导致潜伏期延长;此外,大量血浆中输注的单采血小板,和/或患有血液系统恶性肿瘤的受者的免疫反应,可能有助于受者建立 HBV 感染。这得到了日本三例先前记录的由 ID-NAT 阴性供体血液制品引起的输血传播 HBV 感染病例的分析的支持。

结论

对于来自 ID-NAT 阴性 HBV 窗口期供体的血液成分输注后,可能需要更长时间(>3 个月)持续监测 HBV 感染。

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