Sirolimus to treat chronic and steroid‐resistant allograft rejection‐related fibrosis in pediatric liver transplantation

Author:

Quintero Bernabeu Jesús1ORCID,Juamperez Goñi Javier1,Mercadal Hally Maria1,Padros Fornieles Crsitina1,Ortega López Juan2,Larrarte King Mauricio1,Molino Gahete José A.3,Salcedo Allende María T.4,Hidalgo Llompart Ernest5,Bilbao Aguirre Itxarone5,Charco Torra Ramon5

Affiliation:

1. Pediatric Hepatology and Liver Transplant Department, ERN Rare Liver ‐ ERN TrasplantChild Hospital Universitari Vall d'Hebron Barcelona Spain

2. Pediatric Intensive Care Unit Hospital Universitari Vall d'Hebron Barcelona Spain

3. Pediatric Surgery Department Hospital Universitari Vall d'Hebron Barcelona Spain

4. Histology Department Hospital Universitari Vall d'Hebron Barcelona Spain

5. HPB Surgery and Transplants Hospital Universitari Vall d'Hebron Barcelona Spain

Abstract

AbstractThis study aimed to report our experience with the use of (SRL) in pediatric liver transplant patients with chronic rejection or steroid‐resistant rejection with hepatic fibrosis, focusing on their histological evolution. All pediatric liver transplant recipients who received off‐label treatment with SRL for chronic ductopenic rejection or cortico‐resistant rejection between July 2003 and July 2022 were included in the study. All nine patients included in the study showed improvement in liver enzymes and cholestasis parameters as soon as 1‐month after post‐SRL introduction. A decrease in fibrosis stage was observed in 7/9 (77.7%) patients at 36 months. All but one patient experienced an improvement in the Rejection Activity Index and ductopenia at 12 months. A single patient had to discontinue SRL treatment owing to nephrotic proteinuria. In conclusion, SRL may be a safe and effective treatment for chronic and steroid‐resistant rejection and may improve allograft rejection‐related fibrosis and ductal damage.

Publisher

Wiley

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