AUTHOR=Matthews Philippa C. , Campbell Cori , Săndulescu Oana , Matičič Mojca , Ruta Simona Maria , Rivero-Juárez Antonio , van Welzen Berend Joost , Tan Boun Kim , Garcia Federico , Gherlan George Sebastian , Çınar Güle , Hasanoğlu İmran , Gmizić Ivana , Nicolini Laura Ambra , Santos Lurdes , Sargsyants Narina , Velikov Petar , Habibović Selma , Fourati Slim , Židovec-Lepej Snježana , Herder Vanessa , Dudman Susanne , Miron Victor Daniel , Irving William , Şahin Gülşen Özkaya , and ESCMID Study Group for Viral Hepatitis (ESGVH) TITLE=Acute severe hepatitis outbreak in children: A perfect storm. What do we know, and what questions remain? JOURNAL=Frontiers in Pharmacology VOLUME=13 YEAR=2022 URL=https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2022.1062408 DOI=10.3389/fphar.2022.1062408 ISSN=1663-9812 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.