May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
Mycophenolate mofetil (MMF) is a highly effective and safe immunosuppressive agent for the treatment of uveitis
Author Affiliations & Notes
  • M. Zierhut
    Department Ophthalmology, University of Tubingen, Tubingen, Germany
  • M. Huber
    Department Ophthalmology, University of Tubingen, Tubingen, Germany
  • N. Stuebiger
    Department Ophthalmology, University of Tubingen, Tubingen, Germany
  • C. Deuter
    Department Ophthalmology, University of Tubingen, Tubingen, Germany
  • K. Siepmann
    Department Ophthalmology, University of Tubingen, Tubingen, Germany
  • Footnotes
    Commercial Relationships  M. Zierhut, None; M. Huber, None; N. Stuebiger, None; C. Deuter, None; K. Siepmann, None.
  • Footnotes
    Support  none
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 3371. doi:
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      M. Zierhut, M. Huber, N. Stuebiger, C. Deuter, K. Siepmann; Mycophenolate mofetil (MMF) is a highly effective and safe immunosuppressive agent for the treatment of uveitis . Invest. Ophthalmol. Vis. Sci. 2004;45(13):3371.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose: We evaluated the outcomes of patients with different forms of chronic uveitis treated with MMF as an immunomodulatory and steroid–sparing agent. The multi–system side effects that arise after long–term treatment with corticosteroids and other immunosuppressants prompted us to use MMF. MMF is a selective inhibitor of inosine monophosphate dehydrogenase thus blocking purine synthesis via the de novo pathway preferentially used by T and B lymphocytes. Methods: Between 1998 and 2003, 106 patients were treated for uveitis (anterior n=26, intermediate n=51, posterior n= 23, panuveitis n=6). Treatment duration was between 1 and 3 years. Patient charts were analysed according to a standardized evaluation protocol. Results: In 95 patients MMF was combined with Prednisolone in a dosage of between 2.5 to 10 mg/day. In 8 patients MMF was used as a monotherapy and in 3 cases one further systemic immunosuppressant was required. The frequency of recurrences was 1 or less in 92 patients, 2 in 6 cases and 3 or greater in 8 patients. The most frequently observed side effects were gastrointestinal upset (15%), followed by eczema (9.3%), fatigue (5.7%), headache (5%), and hair loss (3.5%). Other side effects were sporadic. Most of these phenomena were transitory. 42 patients experienced no side effects at all. In 4 patients MMF was judged ineffective due to recurrences or persistent macular edema. Conclusions: MMF is a safe, effective immunosuppressant in patients with uveitis. We provide evidence that MMF controls the disease in the majority of patients with an acceptable profile of side effects.

Keywords: uveitis–clinical/animal model • immunomodulation/immunoregulation • autoimmune disease 
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