https://pubmed.ncbi.nlm.nih.gov/36506522/ Hepatitis

Review

Front Pharmacol. 2022 Nov 25;13:1062408.
doi: 10.3389/fphar.2022.1062408.eCollection 2022.

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

Philippa C Matthews 1 2 3, Cori Campbell 4, Oana Săndulescu 5, Mojca Matičič 6, Simona Maria Ruta 7, Antonio Rivero-Juárez 8, Berend Joost van Welzen 9, Boun Kim Tan 10, Federico Garcia 11, George Sebastian Gherlan 12, Güle Çınar 13, İmran Hasanoğlu 14, Ivana Gmizić 15, Laura Ambra Nicolini 16, Lurdes Santos 17, Narina Sargsyants 18, Petar Velikov 19, Selma Habibović 20, Slim Fourati 21, Snježana Židovec-Lepej 22, Vanessa Herder 23, Susanne Dudman 24, Victor Daniel Miron 25, William Irving 26, Gülşen Özkaya Şahin 27 28; and ESCMID Study Group for Viral Hepatitis (ESGVH)

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.