Common mechanisms in pediatric acute liver failure

Jake P Mann, Dominic Lenz, Zania Stamataki, Deirdre Kelly

Research output: Contribution to journalReview articlepeer-review

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Abstract

Acute liver failure (ALF) is a rare but potentially fatal disease in children. The etiology is multifactorial, including infection, autoimmune, and genetic disorders, as well as indeterminate hepatitis, which has a higher requirement for liver transplantation. Activation of the innate and adaptive immune systems leads to hepatocyte-specific injury which is mitigated by T regulatory cell activation. Recovery of the native liver depends on activation of apoptotic and regenerative pathways, including the integrated stress response (ISR; e.g., PERK), p53, and HNF4α. Loss-of-function mutations in these pathways cause recurrent ALF in response to non-hepatotropic viruses. Deeper understanding of these mechanisms will lead to improved diagnosis, management, and outcomes for pediatric ALF.

Original languageEnglish
Number of pages13
JournalTrends in Molecular Medicine
Early online date7 Dec 2022
DOIs
Publication statusE-pub ahead of print - 7 Dec 2022

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Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

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