Increased seroprevalence of HAV and parvovirus B19 in children and of HEV in adults at diagnosis of autoimmune hepatitis

Richard Taubert*, Jana Diestelhorst, Norman Junge, Martha M. Kirstein, Sven Pischke, Arndt Vogel, Heike Bantel, Ulrich Baumann, Michael P. Manns, Heiner Wedemeyer, Elmar Jaeckel

*Corresponding author for this work

Abstract

Preceding viral infections have mostly been described in autoimmune hepatitis (AIH) in single cases. We aimed to identify viral infections that potentially trigger AIH, as suggested for hepatitis E virus (HEV) infections. Therefore, antibodies against hepatitis A (HAV), B, C and E viruses; hepatotropic herpesviruses; and parvovirus B19 (PVB19) were analyzed retrospectively in 219 AIH patients at diagnosis, 356 patients with other liver diseases and 89 children from our center. Untreated adult AIH (aAIH) patients showed higher anti-HEV seroprevalences at diagnosis than patients with other liver diseases. Untreated aAIH patients had no increased incidence of previous hepatitis A, B or C. Antibodies against hepatotropic herpesviruses in untreated AIH were in the range published for the normal population. Untreated pediatric AIH (pAIH) patients had evidence of more previous HAV and PVB19 infections than local age-matched controls. The genetic AIH risk factor HLA DRB1*03:01 was more frequent in younger patients, and DRB1*04:01 was more frequent in middle-aged patients without an obvious link to virus seropositivities. Pediatric and adult AIH seem to be distinct in terms of genetic risk factors and preceding viral infections. While associations cannot prove causal relations, the results suggest that hepatotropic virus infections could be involved in AIH pathogenesis.

Original languageEnglish
Article number17452
JournalScientific Reports
Volume8
Issue number1
ISSN2045-2322
DOIs
Publication statusPublished - 01.12.2018

Funding

We thank Dr. Christina Poethko-Mueller from the Department of Epidemiology and Health Monitoring at the Robert Koch Institute (Berlin/Germany) for the statistical analysis of the hepatitis A serology results from the KIGGS and DEGS1 studies, and we thank the Robert Koch Institute for contributing the health monitoring data. The work was supported by grants from the German Research Foundation (KFO250 project 7; SFB TR 127 project A4). J.D. was supported by the “Else-Kröner-Fresenius-Foundation” as part of the M.D. dissertation program (KlinStrucMed), and R.T. was supported by the Young Faculty Program of Hannover Medical School.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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