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Published on: June 26, 2020
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.
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.
Abstract:
During the first half of 2022, the World Health Organization reported an outbreak of acute severe hepatitis of unknown aetiology (AS-Hep-UA) in children, following initial alerts from the United Kingdom (UK) where a cluster of cases was first observed in previously well children aged <6 years. Sporadic cases were then reported across Europe and worldwide, although in most countries incidence did not increase above the expected baseline. There were no consistent epidemiological links between cases, and microbiological investigations ruled out known infectious causes of hepatitis. In this review, we explore the evidence for the role of viral infection, superimposed on a specific host genetic background, as a trigger for liver pathology. This hypothesis is based on a high prevalence of Human Adenovirus (HAdV) 41F in affected children, together with metagenomic evidence of adeno-associated virus (Adeno-associated viruses)-2, which is a putative trigger for an immune-mediated liver injury. Roles for superantigen-mediated pathology have also been explored, with a focus on the potential contribution of SARS-CoV-2 infection. Affected children also had a high frequency of the MHC allele HLA-DRB1*04:01, supporting an immunological predisposition, and may have been vulnerable to viral coinfections due to disruption in normal patterns of exposure and immunity as a result of population lockdowns during the COVID-19 pandemic. We discuss areas of ongoing uncertainty, and highlight the need for ongoing scrutiny to inform clinical and public health interventions for this outbreak and for others that may evolve in future.
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