Folic acid prevents interferon-induced iron accumulation and ferroptosis and improves liver health in children with biliary atresia

Abstract

Background & Aims: Biliary atresia (BA) is an obstructive newborn jaundice disease that leads to liver failure in the majority of affected infants. Viral infection is an important environmental trigger of BA. The aim of the study is to establish how viral infection rewires the cellular and metabolic processes of the digestive systems in at-risk infants and leads to BA development. Methods: Single cell RNA (scRNA) transcriptomes and V(D)J sequences were generated using small intestine and liver biopsies from BA and control infants. Candidate risk genes were identified by genome-wide association study. Patient specimens, mouse model of experimental biliary atresia, and a myeloid-specific Folr2 knockout mice (folr2Mko) were used to determine immune pathologies that lead to BA development. An open label clinical trial was conducted to determine the therapeutic effect of folic acid on post-Kasai outcomes of patients with BA. Results: Type I interferon (IFN-I) signaling is persistently activated in infants with BA. This promotes expression of hepcidin in hepatic TREM2+ macrophages and hepatocytes, which impairs SLC40A1-mediated iron excretion from the small intestine, leading to iron accumulation, lipid peroxidation, dysbiosis and folic acid deficiency. By genetic ablation of Folr2, we show that folinate supplementation halts persistent IFN-I activation and suppresses hepcidin expression by TREM2+ macrophages. In an open label clinical study, folic acid supplementation decreased post-Kasai cholangitis incidences and liver transplantation rates by 70%. Conclusion: Persistent IFN-I signaling plays a critical role in virally induced pathological jaundice in infants, and that folic acid supplementation is an effective therapy for BA.

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

Chinese clinical trial, ChiCTR2100050992

Funding Statement

This study was funded by The National Natural Science Foundation of China,Basic and Applied Basic Research Foundation of Guangdong Province, Basic and Applied Basic Research Foundation of Guangdong Province, Natural Science Fund of Guangdong Province, Research Fund of Guangzhou Women and Children Medical Center.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Medical Ethics Committee of Guangzhou Women and Children's Medical Center gave ethical approval for this work.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Comments (0)

No login
gif