1. Academic Validation
  2. A locally active antiinflammatory macrolide (MLD987) for inhalation therapy of asthma

A locally active antiinflammatory macrolide (MLD987) for inhalation therapy of asthma

  • J Med Chem. 2004 Sep 23;47(20):4950-7. doi: 10.1021/jm031101l.
Rene Hersperger 1 Karl-Heinz Buchheit Salvatore Cammisuli Albert Enz Olivier Lohse Monique Ponelle Walter Schuler Alain Schweitzer Christoph Walker Hartmut Zehender Gerhard Zenke Alfred G Zimmerlin Markus Zollinger Lazzaro Mazzoni John R Fozard
Affiliations

Affiliation

  • 1 Novartis Institutes for BioMedical Research and Novartis Pharma Development, CH-4002 Basle, Switzerland. rene.hersperger@pharma.novartis.com
Abstract

One of the characteristic features of asthma is a persistent pulmonary inflammation, with increased numbers of eosinophils and activated T-lymphocytes in the airways. T-helper cells of the Th2 phenotype play a pivotal role in the pathogenesis of asthma, and they are believed to orchestrate the asthmatic response by releasing a wide repertoire of cytokines. Herein, we describe the design, synthesis, and evaluation in models of allergic asthma of a locally active T-cell modulator, MLD987 (1). Compound 1 is a potent immunosuppressant that inhibits the activation, proliferation, and release of cytokines from T-cells with IC(50) values in the low nanomolar range. In a Brown-Norway rat model of allergic asthma, 1, when given into the airways by intratracheal administration (ED(50) = 1 mg/kg) or by inhalation (ED(50) = 0.4 mg/kg), potently reduced the influx of leukocytes into bronchoalveolar lavage fluid samples obtained from antigen-challenged Animals. In contrast, 1 had an appreciably weaker activity in this model when given orally or intravenously. Pharmacokinetic evaluation in rat and rhesus monkey showed that 1 had both a low oral (2-4%) and a low pulmonary (7%, monkey) bioavailability. These findings are consistent with a local site of action of the compound and rule out that its antiinflammatory activity in the lung was caused by systemically absorbed material, which had been swallowed during inhalation or which had entered the circulation via the airways. Local administration and the metabolically soft structure of 1, which favors rapid systemic metabolism to less immunosuppressive metabolite 2, are the main reasons for the low exposure and weak systemic activity of the compound. Administration of a locally active compound such as 1, by inhalation, should reduce systemic side effects. Our results indicate that 1 has the potential to serve as an alternative to inhaled glucocorticosteroids for the long-term therapy of asthma of all grades of severity.

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