TY - JOUR
T1 - Genomic investigations of unexplained acute hepatitis in children
AU - DIAMONDS Consortium
AU - PERFORM Consortium
AU - ISARIC 4C Investigators
AU - Morfopoulou, Sofia
AU - Buddle, Sarah
AU - Torres Montaguth, Oscar Enrique
AU - Atkinson, Laura
AU - Guerra-Assunção, José Afonso
AU - Moradi Marjaneh, Mahdi
AU - Zennezini Chiozzi, Riccardo
AU - Storey, Nathaniel
AU - Campos, Luis
AU - Hutchinson, J. Ciaran
AU - Counsell, John R.
AU - Pollara, Gabriele
AU - Roy, Sunando
AU - Venturini, Cristina
AU - Antinao Diaz, Juan F.
AU - Siam, Ala’a
AU - Tappouni, Luke J.
AU - Asgarian, Zeinab
AU - Ng, Joanne
AU - Hanlon, Killian S.
AU - Lennon, Alexander
AU - McArdle, Andrew
AU - Czap, Agata
AU - Rosenheim, Joshua
AU - Andrade, Catarina
AU - Anderson, Glenn
AU - Lee, Jack C.D.
AU - Williams, Rachel
AU - Williams, Charlotte A.
AU - Tutill, Helena
AU - Bayzid, Nadua
AU - Martin Bernal, Luz Marina
AU - Macpherson, Hannah
AU - Montgomery, Kylie Ann
AU - Moore, Catherine
AU - Templeton, Kate
AU - Neill, Claire
AU - Holden, Matt
AU - Gunson, Rory
AU - Shepherd, Samantha J.
AU - Shah, Priyen
AU - Cooray, Samantha
AU - Voice, Marie
AU - Steele, Michael
AU - Fink, Colin
AU - Whittaker, Thomas E.
AU - Santilli, Giorgia
AU - Gissen, Paul
AU - Shen, Ching Fen
AU - Wang, Shih Min
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/5/18
Y1 - 2023/5/18
N2 - Since its first identification in Scotland, over 1,000 cases of unexplained paediatric hepatitis in children have been reported worldwide, including 278 cases in the UK1. Here we report an investigation of 38 cases, 66 age-matched immunocompetent controls and 21 immunocompromised comparator participants, using a combination of genomic, transcriptomic, proteomic and immunohistochemical methods. We detected high levels of adeno-associated virus 2 (AAV2) DNA in the liver, blood, plasma or stool from 27 of 28 cases. We found low levels of adenovirus (HAdV) and human herpesvirus 6B (HHV-6B) in 23 of 31 and 16 of 23, respectively, of the cases tested. By contrast, AAV2 was infrequently detected and at low titre in the blood or the liver from control children with HAdV, even when profoundly immunosuppressed. AAV2, HAdV and HHV-6 phylogeny excluded the emergence of novel strains in cases. Histological analyses of explanted livers showed enrichment for T cells and B lineage cells. Proteomic comparison of liver tissue from cases and healthy controls identified increased expression of HLA class 2, immunoglobulin variable regions and complement proteins. HAdV and AAV2 proteins were not detected in the livers. Instead, we identified AAV2 DNA complexes reflecting both HAdV-mediated and HHV-6B-mediated replication. We hypothesize that high levels of abnormal AAV2 replication products aided by HAdV and, in severe cases, HHV-6B may have triggered immune-mediated hepatic disease in genetically and immunologically predisposed children.
AB - Since its first identification in Scotland, over 1,000 cases of unexplained paediatric hepatitis in children have been reported worldwide, including 278 cases in the UK1. Here we report an investigation of 38 cases, 66 age-matched immunocompetent controls and 21 immunocompromised comparator participants, using a combination of genomic, transcriptomic, proteomic and immunohistochemical methods. We detected high levels of adeno-associated virus 2 (AAV2) DNA in the liver, blood, plasma or stool from 27 of 28 cases. We found low levels of adenovirus (HAdV) and human herpesvirus 6B (HHV-6B) in 23 of 31 and 16 of 23, respectively, of the cases tested. By contrast, AAV2 was infrequently detected and at low titre in the blood or the liver from control children with HAdV, even when profoundly immunosuppressed. AAV2, HAdV and HHV-6 phylogeny excluded the emergence of novel strains in cases. Histological analyses of explanted livers showed enrichment for T cells and B lineage cells. Proteomic comparison of liver tissue from cases and healthy controls identified increased expression of HLA class 2, immunoglobulin variable regions and complement proteins. HAdV and AAV2 proteins were not detected in the livers. Instead, we identified AAV2 DNA complexes reflecting both HAdV-mediated and HHV-6B-mediated replication. We hypothesize that high levels of abnormal AAV2 replication products aided by HAdV and, in severe cases, HHV-6B may have triggered immune-mediated hepatic disease in genetically and immunologically predisposed children.
UR - http://www.scopus.com/inward/record.url?scp=85151469478&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85151469478&partnerID=8YFLogxK
U2 - 10.1038/s41586-023-06003-w
DO - 10.1038/s41586-023-06003-w
M3 - Article
C2 - 36996872
AN - SCOPUS:85151469478
SN - 0028-0836
VL - 617
SP - 564
EP - 573
JO - Nature
JF - Nature
IS - 7961
ER -