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Commentary on “Outcomes of Allogenic Umbilical Cord Mesenchymal Stem Cell Infusion for Liver Cirrhosis Due to Biliary Atresia After Kasai Operation” JPEDSURG-D-25-00654R2
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Read the article on jpedsurg.org ↗Article · Sep 2025 · 1 min read
In brief
In brief
This commentary discusses Vietnamese research on umbilical cord mesenchymal stem cell infusion as adjunctive therapy for biliary atresia patients post-Kasai operation. The study addresses a critical unmet need in managing progressive liver fibrosis in infants with advanced disease at presentation.
- Allogeneic umbilical cord mesenchymal stem cells show promise as adjunct therapy for post-Kasai biliary atresia patients with advanced fibrosis.
- Study cohort had late Kasai operations (median 81 days) with 75% showing severe fibrosis (METAVIR F3-F4) at baseline.
- Cell-based therapy represents novel approach to address liver fibrosis progression in biliary atresia, a condition with limited treatment options.
- Vietnamese research team demonstrates feasibility of stem cell infusion in pediatric post-portoenterostomy liver disease management.
Written by the GCMD Library team from the article.
The Vietnamese team led by Prof. Nguyen Thanh Liem contributes important work based on the cutting-edge application of cell-based therapy in biliary atresia (BA). This is, potentially, an exciting area working in a field characterised essentially by complete failure to influence the morbid march of liver fibrosis and ultimately failure of the post-Kasai (KPE) portoenterostomy child born with BA [1]. The 16 infants in the study group underwent KPE at a relatively advanced median age of 81 days with 75 % having severe fibrosis (METAVIR F3 or F4 (cirrhosis)) on the initial liver biopsy.
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