Acute severe hepatitis outbreak in children: A perfect storm. What do we know, and what questions remain?

Philippa C Matthews1,2,3, Cori Campbell4, Oana Săndulescu5

  • 1The Francis Crick Institute, London, United Kingdom.

Frontiers in Pharmacology
|December 12, 2022
PubMed

Insights

Severe hepatitis in children was linked to Human Adenovirus 41F and adeno-associated virus-2, potentially triggered by immune responses in genetically predisposed individuals. COVID-19 lockdowns may have increased vulnerability to these viral coinfections.

Area of Science:

  • Pediatric Infectious Diseases
  • Hepatology
  • Immunology

Background:

  • An outbreak of acute severe hepatitis of unknown aetiology (AS-Hep-UA) occurred in children globally in 2022.
  • Microbiological investigations ruled out common infectious causes, prompting research into novel etiologies.

Purpose of the Study:

  • To review evidence supporting viral infections, particularly Human Adenovirus (HAdV) 41F, as a trigger for pediatric hepatitis.
  • To explore the role of host genetic factors and immune responses in AS-Hep-UA pathogenesis.

Main Methods:

  • Review of existing literature and case data on the 2022 pediatric hepatitis outbreak.
  • Analysis of microbiological findings, including Human Adenovirus (HAdV) 41F and adeno-associated virus-2 prevalence.
  • Examination of host genetic factors, such as HLA-DRB1*04:01, and potential links to SARS-CoV-2.

Main Results:

  • High prevalence of Human Adenovirus (HAdV) 41F detected in affected children.
  • Metagenomic evidence suggested adeno-associated virus-2 involvement in immune-mediated liver injury.
  • Association found between affected children and the MHC allele HLA-DRB1*04:01, indicating genetic predisposition.

Conclusions:

  • Viral infections, specifically HAdV 41F and potentially AAV-2, superimposed on a susceptible host genetic background, are a leading hypothesis for AS-Hep-UA.
  • Immune-mediated liver injury and potential contributions from SARS-CoV-2 are considered.
  • COVID-19 pandemic-related disruptions may have influenced susceptibility to viral coinfections.

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