Diagnostic Performance of Five Assays for Anti-Hepatitis E Virus IgG and IgM in a Large Cohort Study

Author:

Norder Heléne1,Karlsson Marie1,Mellgren Åsa2,Konar Jan3,Sandberg Elisabeth1,Lasson Anders4,Castedal Maria5,Magnius Lars6,Lagging Martin1

Affiliation:

1. Department of Infectious Medicine, Institute of Biomedicine at Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

2. Clinic of Infectious Diseases, Södra Älvsborgs Hospital, Borås, Sweden

3. Department of Transfusion Medicine, Sahlgrenska University Hospital, Gothenburg, Sweden

4. Department of Internal Medicine, Södra Älvsborgs Hospital, Borås, Sweden

5. Transplant Institute, Sahlgrenska University Hospital and Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

6. Ulf Lundahl Foundation, Stockholm, Sweden

Abstract

ABSTRACT Determination of anti-hepatitis E virus (anti-HEV) antibodies is still enigmatic. There is no gold standard, and results obtained with different assays often diverge. Herein, five assays were compared for detection of anti-HEV IgM and IgG. Serum samples from 500 Swedish blood donors and 316 patients, of whom 136 had suspected HEV infection, were analyzed. Concordant results for IgM and IgG with all assays were obtained only for 71% and 70% of patients with suspected hepatitis E, respectively. The range of sensitivity for anti-HEV detection was broad (42% to 96%); this was reflected in the detection limit, which varied up to 19-fold for IgM and 17-fold for IgG between assays. HEV RNA was analyzed in all patients and in those blood donors reactive for anti-HEV in any assay, and it was found in 26 individuals. Among all of the assays, both anti-HEV IgG and IgM were detected in 10 of those individuals. Twelve had only IgG and, in 7 of those 12, IgG was only detected with the two most sensitive assays. Three of the HEV-RNA-positive samples were negative for anti-HEV IgM and IgG in all assays. With the two most sensitive assays, anti-HEV IgG was identified in 16% of the blood donor samples and in 66% of patients with suspected HEV infection. Because several HEV-RNA-positive samples had only anti-HEV IgG without anti-HEV IgM or lacked anti-HEV antibodies, analysis for HEV RNA may be warranted as a complement in the laboratory diagnosis of ongoing HEV infection.

Funder

EU 7th framework programme

Sahlgrenska Univesity Hospital

FoU-rådet Södra Älvsborg

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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