TY - JOUR
T1 - Acute severe hepatitis outbreak in children
T2 - A perfect storm. What do we know, and what questions remain?
AU - Matthews, Philippa C
AU - Campbell, Cori
AU - Săndulescu, Oana
AU - Matičič, Mojca
AU - Ruta, Simona Maria
AU - Rivero-Juárez, Antonio
AU - van Welzen, Berend Joost
AU - Tan, Boun Kim
AU - Garcia, Federico
AU - Gherlan, George Sebastian
AU - Çınar, Güle
AU - Hasanoğlu, İmran
AU - Gmizić, Ivana
AU - Nicolini, Laura Ambra
AU - Santos, Lurdes
AU - Sargsyants, Narina
AU - Velikov, Petar
AU - Habibović, Selma
AU - Fourati, Slim
AU - Židovec-Lepej, Snježana
AU - Herder, Vanessa
AU - Dudman, Susanne
AU - Miron, Victor Daniel
AU - Irving, William
AU - Şahin, Gülşen Özkaya
N1 - Funding Information:
PM receives core funding from the Francis Crick Institute, holds a Wellcome fellowship (grant ref 110110/Z/15/Z), and has funding support from UCL NIHR Biomedical Research Centre. CC receives PhD fellowship funding from the Nuffield Department of Medicine and GSK. The funders had no role in design, writing or decision to publish.
Publisher Copyright:
Copyright © 2022 Matthews, Campbell, Săndulescu, Matičič, Ruta, Rivero-Juárez, van Welzen, Tan, Garcia, Gherlan, Çınar, Hasanoğlu, Gmizić, Nicolini, Santos, Sargsyants, Velikov, Habibović, Fourati, Židovec-Lepej, Herder, Dudman, Miron, Irving and Şahin.
PY - 2022/11/25
Y1 - 2022/11/25
N2 - 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.
AB - 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.
KW - adeno-associated virus
KW - adenovirus
KW - aetiology
KW - epidemiology
KW - hepatitis
KW - liver
KW - outbreak
KW - paediatric
UR - http://www.scopus.com/inward/record.url?scp=85143788876&partnerID=8YFLogxK
U2 - 10.3389/fphar.2022.1062408
DO - 10.3389/fphar.2022.1062408
M3 - Review article
C2 - 36506522
SN - 1663-9812
VL - 13
JO - Frontiers in Pharmacology
JF - Frontiers in Pharmacology
M1 - 1062408
ER -