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急性暴发性肝衰竭中的人细小病毒B19感染

Human parvovirus B19 infection in acute fulminant liver failure.

作者信息

Karetnyi Y V, Beck P R, Markin R S, Langnas A N, Naides S J

机构信息

Division of Rheumatology, Department of Internal Medicine, University of Iowa, Iowa City, USA.

出版信息

Arch Virol. 1999;144(9):1713-24. doi: 10.1007/s007050050699.

Abstract

We previously reported detection of human parvovirus B19 DNA in livers from patients requiring transplantation for acute fulminant liver failure. In this study, we used immune adherence PCR (IA-PCR) to bind B19 virions in recipient native liver onto solid phase with specific monoclonal antibodies followed by PCR amplification of virion DNA. IA-PCR had sensitivity and specificity similar to conventional PCR. We examined liver tissue from 16 patients with non-A, non-B, non-C, non-E (NA-E) acute fulminant liver failure (AFLF) (6 of unknown etiology associated with aplastic anemia (AA), 4 of unknown etiology without AA; and 6 patients with AFLF of known etiology). IA-PCR detected B19 virions in 5 of 6 (83%) of livers from patients with idiopathic NA-E AFLF associated with AA and in 2 of 3 (75%) without AA, compared to 1 of 6 (17%) of livers from patients with AFLF of known etiology and to 6 of 34 (18%) of 34 control patients with chronic or neoplastic liver disease. Viral mRNA encoding the structural protein was detected in the liver tissue from three B19 IA-PCR positive patients with AFLF. Detection of B19 virions and mRNA for capsid proteins provided strong evidence for B19 infection during the course of NA-E AFLF and argues for involvement of B19 virus in liver injury.

摘要

我们之前报道过,在因急性暴发性肝衰竭而需要进行肝移植的患者肝脏中检测到了人细小病毒B19 DNA。在本研究中,我们使用免疫粘附PCR(IA-PCR),通过特异性单克隆抗体将受体自身肝脏中的B19病毒颗粒结合到固相上,随后对病毒颗粒DNA进行PCR扩增。IA-PCR的敏感性和特异性与传统PCR相似。我们检查了16例非A、非B、非C、非E(NA-E)急性暴发性肝衰竭(AFLF)患者的肝组织(6例病因不明且与再生障碍性贫血(AA)相关,4例病因不明但无AA;以及6例病因已知的AFLF患者)。与6例病因已知的AFLF患者肝脏中的1例(17%)以及34例慢性或肿瘤性肝病对照患者中的6例(18%)相比,IA-PCR在6例与AA相关的特发性NA-E AFLF患者的肝脏中有5例(83%)检测到B19病毒颗粒,在3例无AA的患者中有2例(75%)检测到。在3例B19 IA-PCR阳性的AFLF患者的肝组织中检测到了编码结构蛋白的病毒mRNA。B19病毒颗粒和衣壳蛋白mRNA的检测为NA-E AFLF病程中B19感染提供了有力证据,并表明B19病毒参与了肝损伤。

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