Journal of Hepatology
Volume 33, Issue 3 , Pages 371-375, September 2000

Mycophenolate mofetil for maintenance of remission in autoimmune hepatitis in patients resistant to or intolerant of azathioprine

  • Paul D Richardson

      Affiliations

    • Department of Gastroenterology, Queen's Medical Centre, University Hospital, Nottingham, UK
  • ,
  • Peter D James

      Affiliations

    • Department of Histopathology, Queen's Medical Centre, University Hospital, Nottingham, UK
  • ,
  • Stephen D Ryder

      Affiliations

    • Department of Gastroenterology, Queen's Medical Centre, University Hospital, Nottingham, UK
    • Corresponding Author InformationStephen D. Ryder, Consultant Hepatologist, Queen's Medical Centre, University Hospital, Nottingham, NG7 2UH, UK. Tel: 44 115 970 9155. Fax: 44 115 942 4554.

Received 7 July 1999; received in revised form 19 January 2000; accepted 28 January 2000.

Abstract 

Background/Aim: Azathioprine is standard therapy for maintenance of remission in patients with autoimmune hepatitis. However, approximately 15% of patients are intolerant of therapy and 10% do not respond to it. There is a need for alternative therapies. We describe here the results of mycophenolate mofetil therapy in patients with autoimmune hepatitis.

Patients: We studied seven patients with type 1 AIH (six female). Three were intolerant of azathioprine and had elevated transaminases and liver histology showing active disease despite prednisolone therapy. Four had been on a dose of 2 mg per kg of azathioprine without complete normalisation of ALT, and had liver biopsies showing active disease. All were treated with mycophenolate 1 g bd and were followed for a median of 46 months (21–59). End points were improvement in histological inflammation, ALT and prednisolone dose.

Results: Five of the seven (71%) patients had normal transaminases after 3 months of treatment. The steroid dose fell from a median of 20 mg per day to 2 mg per day at 9 months (p=0.0001) and the hepatic activity index fell from median 11 to 3 (p=0.001) after 7 months of therapy. One patient required dose reduction because of a fall in white cell count. No other adverse effects were seen.

Conclusions: Mycophenolate mofetil is effective and well tolerated in patients with type 1 AIH who are intolerant of, or do not respond to, azathioprine.

Keywords:  Immunomodulation, Mycopenoloic acid, Therapy

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PII: S0168-8278(00)80271-8

Journal of Hepatology
Volume 33, Issue 3 , Pages 371-375, September 2000