Early steroids after pediatric liver transplantation protect against T-cell–mediated rejection: Results from the ChilSFree study

Author:

Goldschmidt Imeke1ORCID,Chichelnitskiy Evgeny2ORCID,Götz Juliane1,Rübsamen Nicole3ORCID,Karch André3ORCID,Jäger Veronika3,Kelly Deirdre4ORCID,Lloyd Carla4ORCID,Debray Dominique5ORCID,Girard Muriel5,d’ Antiga Lorenzo6ORCID,di Giorgio Angelo6,Hierro Loreto7ORCID,Pawlowska Joana8,Klaudel-Dreszler Maja8ORCID,McLin Valerie9ORCID,Korff Simona9ORCID,Falk Christine2ORCID,Baumann Ulrich1

Affiliation:

1. Department of Paediatric Liver, Kidney and Metabolic Diseases, Division of Paediatric Gastroenterology and Hepatology, Hannover Medical School, Hannover, Germany

2. Institute of Transplant Immunology, Hannover Medical School, Hannover, Germany

3. Institute of Epidemiology and Social Medicine, University of Münster, Münster, Germany

4. Liver Unit, Birmingham Women’s & Children’s Hospital, University of Birmingham, Birmingham, UK

5. Pediatric Hepatology Unit, Hôpital Necker-Enfants malades, Paris, France

6. Paediatric Liver, GI and Transplantation, Ospedali Riuniti di Bergamo, Bergamo, Italy

7. Servicio de Hepatología y Transplante, Hospital Infantil Universitario La Paz Madrid, Madrid, Spain

8. Centrum Zdrowia Dziecka, Al. Dzieci Polskich, Warszawa, Poland

9. Department of Pediatrics, Gynecology, and Obstetrics, Swiss Pediatric Liver Center, University Hospitals Geneva, University of Geneva, Geneva, Switzerland

Abstract

Steroid-free immunosuppression protocols gained popularity in pediatric liver transplantation (pLT) after the introduction of IL-2–receptor blockade for induction therapy. We analyzed the clinical and immunologic outcome data of the multicenter prospective observational ChilSFree study to compare the impact of steroid-free versus steroid-containing immunosuppressive therapy following pLT in a real-life scenario. Two hundred forty-six children [55.3% male, age at pLT median: 2.4 (range: 0.2–17.9) y] transplanted for biliary atresia (43%), metabolic liver disease (9%), acute liver failure (4%), hepatoblastoma (9%), and other chronic end-stage liver diseases (39%) underwent immune monitoring and clinical data documentation over the first year after pLT. Patient and graft survival at 1 year was 98.0% and 92.7%, respectively. Primary immunosuppression was basiliximab induction followed by tacrolimus (Tac) monotherapy (55%), Tac plus steroid tapering over 3 months (29%), or cyclosporine and steroid tapering (7%). One center used intraoperative steroids instead of basiliximab followed by Tac plus mycophenolate mofetil (7% of patients). N = 124 biopsy-proven T-cell–mediated rejections were documented in n = 82 (33.3%) patients. T-cell–mediated rejection occurred early (median: 41 d, range: 3–366 d) after pLT. Patients initially treated with Tac plus steroids experienced significantly fewer episodes of rejection than patients treated with Tac alone (chi-square p<0.01). The use of steroids was associated with earlier downregulation of proinflammatory cytokines interferon (IFN)-γ, Interleukin (IL)-6, CX motif chemokin ligand (CXCL)8, IL-7, and IL-12p70. Both primary immunosuppression with Tac plus steroids and living donor liver transplantation were independent predictors of rejection-free survival 1 year after pLT on logistic regression analysis. Adjunctive steroid therapy after pLT leads to earlier suppression of the post-pLT proinflammatory response and significantly reduced rejection rates during the first year after pLT (15.9%). Fifty-one percent of patients initially treated without steroids remain steroid-free over the first 12 months without rejection.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Transplantation,Hepatology,Surgery

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