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Case report: Acute liver failure in children and the human herpes virus 6-? A factor in the recent epidemic
Suz Warner1,2, Rachel M Brown2,3, Gary M Reynolds1
1Centre for Liver and Gastrointestinal Research at the Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Insights
Human herpes virus 6B (HHV-6B) infection can cause severe acute hepatitis and liver failure in infants. This study highlights the critical need for HHV-6B screening in children with hepatitis and antiviral prophylaxis post-transplant.
Area of Science:
- Pediatrics
- Hepatology
- Virology
Background:
- The 2022 epidemic of acute hepatitis in children prompted investigation into unusual causes.
- Human herpes virus 6B (HHV-6B) and adenovirus-41F were detected in severely affected children during the UK epidemic.
- The lifting of COVID-19 lockdowns coincided with increased childhood infections and systemic complications.
Abstract:
The 2022 worldwide epidemic of acute hepatitis and liver failure in young children has led to a focus on unusual causes for childhood acute hepatitis. In the UK epidemic, human herpes virus subtype 6B (HHV-6B) was detected along with adenovirus subtype-41F in severely affected children, especially in those requiring liver transplantation (LT). The lifting of COVID lock-down measures has coincided with the rise in these common childhood infections with a higher than expected rate of systemic complications. The sudden exposure of young children to common childhood infections from which they were protected during the pandemic may have induced an abnormal immune mediated response potentiated by multiple pathogen exposure. Primary HHV-6 infection is one such common childhood infection. Classically known as Roseola infantum due to the appearance of a widespread erythematous rash on fever subsidence (exanthema subitem), it has a peak incidence of 6-12 months of age and almost all children will have been infected by age 2. It is the virus most frequently associated with febrile convulsions but the more serious complications of hepatitis and liver failure are rare. We report on the historic cases of three female infants who had suspected primary HHV-6B infection, acute hepatitis and rapid progression to acute liver failure (ALF) requiring LT. Appearances of their native liver were identical to those described in children in the recent hepatitis epidemic. Deteriorating clinical trajectories of recurrent graft hepatitis and rejection-like episodes followed and all three succumbed to graft failure with HHV-6B detected posthumously in their liver allografts. Our case series and the serious complications observed with the recent rise in common childhood infections is a reminder that these routinely encountered pathogens can be deadly especially in the young immunologically untrained. We advocate for HHV-6 to be screened for routinely in children with acute hepatitis and the use of effective HHV-6 anti-viral prophylaxis to prevent recurrence post-transplant.
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