AUTHOR=Haller Wolfram , Hodson James , Brown Rachel , Lloyd Carla , Hubscher Stefan , McKiernan Patrick , Kelly Deirdre 

TITLE=The role of immunosuppression in long-term graft hepatitis and fibrosis after paediatric liver transplant – comparison of two treatment protocols

JOURNAL=Frontiers in Transplantation

VOLUME=1

YEAR=2023

URL=https://www.frontiersin.org/journals/transplantation/articles/10.3389/frtra.2022.1042676

DOI=10.3389/frtra.2022.1042676

ISSN=2813-2440

ABSTRACT=<sec><title>Background and aims</title><p>We have previously demonstrated high rates of chronic allograft hepatitis and fibrosis in liver transplant patients on long-term cyclosporine monotherapy. We subsequently changed practice to add low-dose prednisolone to maintenance treatment with tacrolimus post-transplant. The aim of the study was to assess the impact of the immunosuppression change on graft histopathology.</p></sec><sec><title>Methods</title><p>Patients treated in this era (Tac + Pred, 2000–2009, <italic>N</italic> = 128) were compared to a historical cohort, who had been maintained on a steroid-free, cyclosporine-based regime (CSA-Only, 1985–1996, <italic>N</italic> = 129). Protocol liver biopsies and laboratory tests were performed five- and ten-years post-transplant in both groups.</p></sec><sec><title>Results</title><p>Compared to CSA-Only, the Tac + Pred cohort had significantly lower rates of chronic hepatitis (CH) at five (20% vs. 44%, <italic>p</italic> &lt; 0.001) and ten (15% vs. 67%, <italic>p</italic> &lt; 0.001) years post-transplant, with similar trends observed in inflammation and fibrosis at five years. The Tac + Pred cohort also had significantly lower hepatic transaminases and IgG levels and was less likely to be autoantibody positive at both time points. However, the degree of graft fibrosis at ten years did not differ significantly between eras (<italic>p</italic> = 0.356).</p></sec><sec><title>Conclusion</title><p>Increased immunosuppression effectively reduced chronic allograft hepatitis and fibrosis at five years, suggesting it is an immunologically driven variant of rejection. However, there was no significant reduction in the degree of fibrosis at ten years, indicating a multifactorial origin for long term graft fibrosis.</p></sec>