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恒河猴中戊型肝炎病毒1型和4型的交叉保护作用。

Cross-protection of hepatitis E virus genotypes 1 and 4 in rhesus macaques.

作者信息

Huang Weijin, Zhang Huayuan, Harrison Tim J, Lang Shuhui, Huang Guoyong, Wang Youchun

机构信息

Department of Cell Biology, National Institute for the Control of Pharmaceutical and Biological Products, Beijing, China.

出版信息

J Med Virol. 2008 May;80(5):824-32. doi: 10.1002/jmv.21140.

DOI:10.1002/jmv.21140
PMID:18360896
Abstract

The purpose of this study was to determine cross-protection between HEV genotypes 1 and 4, which are prevalent in China. Fecal suspensions of genotypes 1 and 4 from patients, as well as genotype 4 from swine, were inoculated intravenously into rhesus macaques. Each inoculum contained 5 x 10(4) genome equivalents of HEV. After infection, serum and fecal samples were collected serially and the levels of alanine aminotransferase (ALT) and anti-HEV IgG and IgM in sera, and HEV RNA in fecal samples, were measured. Liver biopsies were carried out. All the infected monkeys (12/12) developed anti-HEV IgG and exhibited fecal shedding of virus. IgM was detected in 11 of 12, and ALT elevation occurred about 2-6 weeks post-inoculation in 10 of 12, infected monkeys. Hepatic histopathology was consistent with acute viral hepatitis and the ORF2 antigen of HEV was detected in the granular cytoplasm of hepatocytes by immunohistochemistry. After recovery from their initial HEV infection, the monkeys were challenged with a heterologous genotype or heterologous source of HEV and monitored for hepatitis and fecal shedding. Previous infection with HEV completely or partially protected against subsequent challenge with a heterologous virus, because 7 of 11 monkeys did not develop HEV infection or shed virus in the feces, and none of them developed hepatitis or exhibited ALT elevation or liver biopsy findings of hepatitis. In conclusion, previous HEV infection may give rise to cross-genotype and cross-host-species protection.

摘要

本研究的目的是确定在中国流行的戊型肝炎病毒1型和4型之间的交叉保护作用。将来自患者的1型和4型以及来自猪的4型粪便悬液静脉注射到恒河猴体内。每个接种物含有5×10⁴个戊型肝炎病毒基因组当量。感染后,连续采集血清和粪便样本,检测血清中丙氨酸转氨酶(ALT)、抗戊型肝炎病毒IgG和IgM水平以及粪便样本中的戊型肝炎病毒RNA。进行肝活检。所有受感染的猴子(12/12)均产生了抗戊型肝炎病毒IgG并出现粪便病毒排出。12只中有11只检测到IgM,12只受感染猴子中有10只在接种后约2 - 6周出现ALT升高。肝脏组织病理学与急性病毒性肝炎一致,通过免疫组织化学在肝细胞的颗粒状细胞质中检测到戊型肝炎病毒的ORF2抗原。在从最初的戊型肝炎病毒感染中恢复后,用异源基因型或异源来源的戊型肝炎病毒对猴子进行攻击,并监测肝炎和粪便排出情况。先前的戊型肝炎病毒感染对随后的异源病毒攻击提供了完全或部分保护,因为11只猴子中有7只未发生戊型肝炎病毒感染或粪便中未排出病毒,且它们均未发生肝炎或出现ALT升高或肝炎的肝活检结果。总之,先前的戊型肝炎病毒感染可能产生交叉基因型和跨宿主物种的保护作用。

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