Bendall R, Ellis V, Ijaz S, Thurairajah P, Dalton H R
Department of Clinical Microbiology, Royal Cornwall Hospital Trust, Truro, Cornwall, UK.
J Med Virol. 2008 Jan;80(1):95-101. doi: 10.1002/jmv.21033.
Sequential sera were collected from 18 acute cases of UK-acquired hepatitis E. The virus strains in all cases were of genotype 3. The IgM and IgG response to acute infection were documented over time using EIA kits based on a peptide antigen, pE2, which is derived from a genotype 1 strain of hepatitis E virus (HEV). Ninety-five percentage of acute sera were IgM positive; after 6 months or more only 12% remained positive. The kit was adapted to quantify the IgG response (in WHO U/ml) and to determine antibody avidity. Following acute infection, anti-HEV IgG concentrations rose between 6.9- and 90-fold. IgG avidity was low (<25%) in most acute sera. After 6 months IgG avidity was greater than 50% in all cases. One patient with a poor IgM response and high avidity antibody in acute sera may have had a second HEV infection. Taken together, these results confirm that the pE2-based EIA kits are suitable for diagnosing acute HEV genotype 3 infection. With simple modifications the IgG kit can measure anti-HEV concentration and avidity, which can be used to confirm acute infection.
从18例在英国感染戊型肝炎的急性病例中采集了系列血清样本。所有病例中的病毒株均为3型。使用基于源自戊型肝炎病毒(HEV)1型毒株的肽抗原pE2的酶免疫分析(EIA)试剂盒,记录了急性感染过程中IgM和IgG的反应随时间的变化情况。95%的急性血清样本IgM呈阳性;6个月或更长时间后,只有12%仍为阳性。该试剂盒经过调整,可定量IgG反应(以WHO U/ml为单位)并测定抗体亲和力。急性感染后,抗HEV IgG浓度升高了6.9至90倍。大多数急性血清样本中的IgG亲和力较低(<25%)。6个月后,所有病例中的IgG亲和力均大于50%。一名急性血清样本中IgM反应较差且抗体亲和力较高的患者可能发生了第二次HEV感染。综上所述,这些结果证实基于pE2的EIA试剂盒适用于诊断急性3型HEV感染。经过简单修改,IgG试剂盒可测量抗HEV浓度和亲和力,可用于确诊急性感染。