Respiratory Medicine
Volume 104, Issue 11 , Pages 1608-1617, November 2010

Omalizumab-induced decrease of FcɛRI expression in patients with severe allergic asthma

  • Pascal Chanez

      Affiliations

    • INSERM U 600, CNRS UMR 6212, Université de la Méditerranée, Marseille F-13009, France
    • Assistance Publique des Hôpitaux de Marseille, Département des Maladies Respiratoires, Marseille F-13009, France
  • ,
  • Cécile Contin-Bordes

      Affiliations

    • Université de Bordeaux, Bordeaux F-33000, France
    • CNRS UMR 5164, IFR 66, Bordeaux F-33000, France
    • Centre Hospitalier Universitaire de Bordeaux, Bordeaux F-33000, France
  • ,
  • Gilles Garcia

      Affiliations

    • Université Paris-Sud 11, Clamart F-92000, France
    • Hôpital Antoine Béclère, Assistance Publique des Hôpitaux de Paris, Service de Pneumologie et Réanimation Respiratoire, Clamart F-92000, France
  • ,
  • Christophe Verkindre

      Affiliations

    • Centre Hospitalier de Béthune, Béthune F-62400, France
  • ,
  • Alain Didier

      Affiliations

    • Centre Hospitalier Universitaire de Toulouse, Hôpital Larrey, Toulouse F-31059, France
  • ,
  • Frédéric De Blay

      Affiliations

    • Pôle de Pathologie Thoracique, Hôpitaux Universitaires de Strasbourg, Strasbourg F-67000, France
    • Université de Strasbourg, Strasbourg F-67000, France
  • ,
  • Manuel Tunon de Lara

      Affiliations

    • Université de Bordeaux, Bordeaux F-33000, France
    • INSERM U855, Bordeaux F-33000, France
  • ,
  • Patrick Blanco

      Affiliations

    • Université de Bordeaux, Bordeaux F-33000, France
    • CNRS UMR 5164, IFR 66, Bordeaux F-33000, France
    • Centre Hospitalier Universitaire de Bordeaux, Bordeaux F-33000, France
  • ,
  • Jean-François Moreau

      Affiliations

    • Université de Bordeaux, Bordeaux F-33000, France
    • CNRS UMR 5164, IFR 66, Bordeaux F-33000, France
    • Centre Hospitalier Universitaire de Bordeaux, Bordeaux F-33000, France
  • ,
  • Philip Robinson

      Affiliations

    • INSERM CIC0005, Bordeaux F-33000, France
  • ,
  • Isabelle Bourdeix

      Affiliations

    • Novartis Pharma S.A.S., Rueil Malmaison F-92506, France
  • ,
  • Patrick Trunet

      Affiliations

    • Novartis Pharma S.A.S., Rueil Malmaison F-92506, France
  • ,
  • Vincent Le Gros

      Affiliations

    • Novartis Pharma S.A.S., Rueil Malmaison F-92506, France
  • ,
  • Marc Humbert

      Affiliations

    • Université Paris-Sud 11, Clamart F-92000, France
    • Hôpital Antoine Béclère, Assistance Publique des Hôpitaux de Paris, Service de Pneumologie et Réanimation Respiratoire, Clamart F-92000, France
  • ,
  • Mathieu Molimard

      Affiliations

    • Université de Bordeaux, Bordeaux F-33000, France
    • Centre Hospitalier Universitaire de Bordeaux, Bordeaux F-33000, France
    • INSERM, Unité 657, IFR 99, Université de Bordeaux, Département de Pharmacologie, CHU de Bordeaux, 33076 Bordeaux cedex, France
    • Corresponding Author InformationCorresponding author. INSERM, Unité 657, IFR 99, Université de Bordeaux, Département de Pharmacologie, CHU de Bordeaux, 33076 Bordeaux cedex, France. Tel.: +33 5 57 57 15 60; fax: +33 5 57 57 46 71.

Received 30 April 2010; accepted 16 July 2010. published online 30 August 2010.

Summary 

Background

It is documented that omalizumab treatment reduces the cell surface expression of immunoglobulin E high-affinity receptor (FcɛRI) on several cell types. This has not been investigated in patients with uncontrolled severe persistent allergic asthma.

Methods

In a double-blind, randomized, placebo-controlled study, patients with severe allergic asthma uncontrolled by high dose inhaled corticosteroids and long-acting β2-agonist received either omalizumab (n = 20) or placebo (n = 11) over 16 weeks at appropriate doses and frequencies. Baseline and end of study (week 16) FcɛRI expression on basophils and plasmacytoid dendritic cells was determined by flow cytometry for the primary endpoint. Secondary efficacy endpoints included asthma control and lung function as part of an initial investigation into the use of FcɛRI expression as a marker of response.

Results

In the omalizumab group, and with respect to placebo, FcɛRI expression was significantly reduced at end of study on basophils (−82.6%, p < 0.01) and plasmacytoid dendritic cells (−44.2%, p = 0.029). FcɛRI expression reduction was not found to be correlated with clinical response.

Conclusions

Long-term omalizumab treatment induced reduction of FcɛRI expression on circulating basophils and plasmacytoid dendritic cells. These changes were not associated with those of clinical features related to severe asthma, which does not support further investigation into its use as a predictive marker of response.

Trial registration

The study was registered with ClinicalTrials.gov (identifier: NCT00454051) and the European Clinical Trials Database, EudraCT (identifier: 2006-003591-35)

Keywords: Basophils, FcɛRI, Omalizumab, Plasmacytoid dendritic cells, Uncontrolled severe allergic asthma

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PII: S0954-6111(10)00332-X

doi:10.1016/j.rmed.2010.07.011

Respiratory Medicine
Volume 104, Issue 11 , Pages 1608-1617, November 2010