A case of transfusion‐transmitted hepatitis E caused by blood from a donor infected with hepatitis E virus via zoonotic food‐borne route

戊型肝炎病毒 病毒学 戊型肝炎 基因型 肝炎 医学 重型肝炎 病毒 输血 生物 免疫学 基因 生物化学
作者
Keiji Matsubayashi,Jong‐Hon Kang,Hidekatsu Sakata,Kazuaki Takahashi,Motohiro Shindo,Masaru Kato,Shin Sato,Toshiaki Kato,Hiroyuki Nishimori,Kunihiko Tsuji,Hiroyuki Maguchi,Junichi Yoshida,Hiroshi Maekubo,Shunji Mishiro,Hisami Ikeda
出处
期刊:Transfusion [Wiley]
卷期号:48 (7): 1368-1375 被引量:288
标识
DOI:10.1111/j.1537-2995.2008.01722.x
摘要

BACKGROUND: Five cases of transfusion transmission of hepatitis E virus (HEV) have been reported so far. The infection routes of the causative donors remain unclear, however. Also, the progress of virus markers in the entire course of HEV infection has not been well documented. STUDY DESIGN AND METHODS: Nucleic acid testing was performed by real-time reverse transcription-polymerase chain reaction targeting the open reading frame 2 region of HEV. Full-length nucleotide sequences of HEV RNA were detected by direct sequencing. RESULTS: Lookback study of a HEV-positive donor revealed that the platelets (PLTs) donated from him 2 weeks previously contained HEV RNA and were transfused to a patient. Thirteen relatives including the donor were ascertained to enjoy grilled pork meats together in a barbecue restaurant 23 days before the donation. Thereafter, his father died of fulminant hepatitis E and the other 6 members showed serum markers of HEV infection. In the recipient, HEV was detected in serum on Day 22 and reached the peak of 7.2 log copies per mL on Day 44 followed by the steep increase of alanine aminotransferase. Immunoglobulin G anti-HEV emerged on Day 67; subsequently, hepatitis was resolved. HEV RNA sequences from the donor and recipient were an identical, Japan-indigenous strain of genotype 4. HEV RNA was detectable up to Day 97 in serum, Day 85 in feces, and Day 71 in saliva. CONCLUSION: A transfusion-transmitted hepatitis E case by blood from a donor infected via the zoonotic food-borne route and the progress of HEV markers in the entire course are demonstrated. Further studies are needed to clarify the epidemiology and the transfusion-related risks for HEV even in industrialized countries.
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