Abstract

Diagnosis of de novo autoimmune hepatitis (AIH) after orthotopic liver transplantation (OLT) is challenging especially in the absence of hyper-γ-globulinemia. Circulating autoantibodies are not sensitive nor specific in de novo AIH but when positive increase the diagnostic probability. We report the discovery of novel liver microsomal (LM) autoantibodies against CYP-2C19 in a 9-year-old boy with “de novo” AIH developed 7 years after OLT. Graft dysfunction presented with hypertransaminasemia (up to 400 IU/L), while serum γ-globulins remained within the normal range for age. Liver histology and response to high dose prednisone (2 mg/kg/day) with the addition of azathioprine therapy further supported the diagnosis of de novo AIH. Autoantibodies investigation by indirect immunofluorescence (IF) on rodent tissues showed a novel staining pattern involving the pericentral liver zone and sparing the renal tissue. Human but not rat liver proteins immunoblotting allowed us to characterize the novel LM antibodies and to identify CYP-2C19 as human antigen. The finding offers insights into the controversial discussion about autoimmunity versus alloreactivity with regard to the pathogenesis of de novo AIH. Correct information on human versus rat tissue antigens tested by methods other than IF for antibodies detection may have significant implications for the correct diagnosis and management of patients followed up after OLT.

Highlights

  • De novo autoimmune hepatitis (AIH) after orthotopic liver transplantation (OLT) should be suspected in any unexplained graft dysfunction, in both children and adults transplanted for an indication different from autoimmune liver diseases [1, 2]

  • A 9-year-old boy developed de novo AIH 7 years after liver transplantation for biliary atresia

  • Liver biopsy revealed a histological picture of portal tracts enlarged by a dense lymphoplasmacytic infiltrate and fibrosis, moderate interface hepatitis with intralobular inflammation, and necrosis in absence of relevant evidence for rejection

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Summary

Introduction

De novo autoimmune hepatitis (AIH) after orthotopic liver transplantation (OLT) should be suspected in any unexplained graft dysfunction, in both children and adults transplanted for an indication different from autoimmune liver diseases [1, 2]. Differential diagnosis with the far more common graft rejection and viral hepatitis is challenging in spite of the diagnostic criteria for de novo AIH proposed in 2006 by the Banff working group [3]. Both typical and atypical circulating autoantibodies have been found to be associated with de novo AIH. Among the typical ones [4, 5], anti-nuclear antibodies (ANA) have been the most frequently detected (42.8%–100%), followed

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