Treatment of childhood asthma with anti-immunoglobulin E antibody (omalizumab).

BACKGROUND AND OBJECTIVE There seems to be a strong causal relationship between allergy and the origins of asthma. Susceptibility to both is determined by a combination of genetics and environment acting through a complex network of cytokines. Nearly 90% of affected children have positive skin tests indicating the presence of specific immunoglobulin E (IgE), with sensitivity to house dust mite, Alternaria, cockroach, cat, and dog most closely linked to the disease. Greater exposure to house dust mite during infancy leads to earlier onset of wheezing, and elevated serum IgE levels correlate with the appearance of asthma symptoms. Specific IgE binds to high-affinity (FcepsilonRI) receptors on mast cells and basophils. The IgE-mediated reactions that follow exposure of sensitized mast cells to an allergen are designated early- and late-phase asthmatic responses (EAR and LAR). EAR is characterized by release of histamine and other preformed mediators within 1 hour of allergen exposure. It is often followed by LAR, an infiltration of the airways by inflammatory cells associated with an episode of more prolonged, and usually more severe airflow obstruction, 4 to 8 hours after antigen exposure. Chronic airway symptoms result from persistent LAR caused by continuous allergen exposure. IgE antibodies are capable of passive transfer of both EAR and LAR sensitivity. IgE-mediated mast cell activation contributes to chronic tissue eosinophilia and airway remodeling, with permanent loss in pulmonary function. Omalizumab (rhuMAb-E25) is a recombinant, humanized, monoclonal anti-IgE antibody of mouse origin developed for the treatment of IgE-mediated diseases. Omalizumab binds to free IgE at the same site as the high-affinity receptor. Although it attaches to free IgE, it does not bind to IgA, IgG, or cell-bound IgE. It therefore does not induce cross-linking of cell-bound IgE, which would lead to the release of allergic mediators. It has been reported to decrease serum IgE levels in a dose-dependent manner, inhibit EAR and LAR, and cause a down-regulation of FcepsilonRI receptors on basophils. Omalizumab has been reported to be safe and effective in improving asthma control and reducing the requirement for oral and inhaled corticosteroids. This double-blind, randomized, placebo-controlled study evaluated the safety, steroid-sparing effects, and impact on disease exacerbations of omalizumab in the treatment of childhood asthma. Methods. Participants were 334 males and premenarchal females aged 6 to 12 years, with moderate to severe allergic asthma requiring treatment with inhaled corticosteroids. During a run-in phase, all children were switched to equivalent doses of beclomethasone dipropionate (BDP), and the dose was adjusted to assure maintenance of asthma control achieved with previous corticosteroid treatment. Children were randomized to subcutaneously administered placebo (N = 109) or omalizumab (N = 225) at a dose based on body weight and initial serum IgE (0.016 mg/kg/IgE [IU/mL] per 4 weeks). BDP dose (initial range 168-420 microg/d) was kept stable for 16 weeks (stable-steroid phase), reduced over 8 weeks to the minimum effective dose (steroid-reduction phase), and maintained constant for the final 4 weeks. RESULTS More participants in the omalizumab group decreased their BDP dose, and their reduction was greater than that of the placebo group (median reduction 100% vs 66.7%). BDP was withdrawn completely in 55% of the omalizumab group versus 39% of the placebo group. The incidence and the frequency of asthma exacerbations requiring treatment with doubling of BDP dose or systemic corticosteroids were lower in the omalizumab group. The treatment differences were statistically significant during the steroid-reduction phase, during which fewer participants in the omalizumab group had asthma exacerbation episodes (18.2% vs 38.5%), and the mean number of episodes per patient was smaller than with placebo (0.42 vs 2.72). Five asthma exacerbations requiring hospitalization all occurred in the placebo group. Participants' and investigators' global evaluations of treatment effectiveness were more favorable for omalizumab than placebo. Investigators rated effectiveness excellent for 31.5% of the omalizumab group versus 16.3% of the placebo group and good for 44.7% of the omalizumab group versus 32.7% of the placebo group. There was little change in asthma symptom scores or spirometry measurements during either the stable-steroid or steroid dose-reduction phase, with minimal differences between the treatment groups. The requirement for rescue medication in the omalizumab group during both the stable-steroid and steroid dose-reduction phases was consistently lower than at baseline. At week 28, the median number of puffs of rescue medication taken daily was 0 in the omalizumab group and 0.46 in the placebo group. The change from baseline was significant in favor of omalizumab. (ABSTRACT TRUNCATED)

[1]  Brigit VanGraafeiland,et al.  National Asthma Education and Prevention Program. , 2002, The Nurse practitioner.

[2]  P. Simpson,et al.  Statistical methods in cancer research , 2001, Journal of surgical oncology.

[3]  M. E. Wohl,et al.  Asthma, steroids, and growth. , 2000, The New England journal of medicine.

[4]  T. Haahtela,et al.  Recombinant humanized mAb-E25, an anti-IgE mAb, in birch pollen-induced seasonal allergic rhinitis. , 2000, The Journal of allergy and clinical immunology.

[5]  S. Galli,et al.  The diverse potential effector and immunoregulatory roles of mast cells in allergic disease. , 2000, The Journal of allergy and clinical immunology.

[6]  P. Newacheck,et al.  Prevalence, impact, and trends in childhood disability due to asthma. , 2000, Archives of pediatrics & adolescent medicine.

[7]  T. Chang The pharmacological basis of anti-IgE therapy , 2000, Nature Biotechnology.

[8]  Salvi Ss,et al.  Treatment of allergic asthma with monoclonal anti-IgE antibody. , 1999 .

[9]  R. Bush,et al.  Treatment of allergic asthma with monoclonal anti-IgE antibody. rhuMAb-E25 Study Group. , 1999, The New England journal of medicine.

[10]  S. Szefler,et al.  The relationships among environmental allergen sensitization, allergen exposure, pulmonary function, and bronchial hyperresponsiveness in the Childhood Asthma Management Program. , 1999, The Journal of allergy and clinical immunology.

[11]  W. Busse,et al.  Early life origins of asthma. , 1999, The Journal of clinical investigation.

[12]  R. Geha,et al.  IgE in asthma and atopy: cellular and molecular connections. , 1999, The Journal of clinical investigation.

[13]  D. Sherrill,et al.  Total serum IgE and its association with asthma symptoms and allergic sensitization among children. , 1999, The Journal of allergy and clinical immunology.

[14]  E. Gelfand,et al.  Role of IgE in the development of allergic airway inflammation and airway hyperresponsiveness – a murine model , 1999, Allergy.

[15]  M. Wills-Karp Immunologic basis of antigen-induced airway hyperresponsiveness. , 1999, Annual review of immunology.

[16]  D. Postma,et al.  Prostaglandin E2 differentially modulates IL-5 gene expression in activated human T lymphocytes depending on the costimulatory signal. , 1998, The Journal of allergy and clinical immunology.

[17]  J. Spahn Is fluticasone propionate superior to the other available inhaled steroids? , 1998, The Journal of asthma : official journal of the Association for the Care of Asthma.

[18]  C. Heusser,et al.  Therapeutic potential of anti-IgE antibodies. , 1997, Current opinion in immunology.

[19]  R. Dockhorn,et al.  Use of an anti-IgE humanized monoclonal antibody in ragweed-induced allergic rhinitis. , 1997, The Journal of allergy and clinical immunology.

[20]  L. Boulet,et al.  Inhibitory effects of an anti-IgE antibody E25 on allergen-induced early asthmatic response. , 1997, American journal of respiratory and critical care medicine.

[21]  H. Boushey,et al.  The effect of an anti-IgE monoclonal antibody on the early- and late-phase responses to allergen inhalation in asthmatic subjects. , 1997, American journal of respiratory and critical care medicine.

[22]  A. Togias,et al.  Down-regulation of Fc(epsilon)RI expression on human basophils during in vivo treatment of atopic patients with anti-IgE antibody. , 1997, Journal of immunology.

[23]  J. Fox,et al.  Tissue distribution and complex formation with IgE of an anti-IgE antibody after intravenous administration in cynomolgus monkeys. , 1996, The Journal of pharmacology and experimental therapeutics.

[24]  H. Hoogsteden,et al.  Effects of fluticasone propionate on methacholine dose-response curves in nonsmoking atopic asthmatics. , 1996, The European respiratory journal.

[25]  S. Holgate The inflammatory basis of asthma and its implications for drug treatment , 1996, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[26]  A Pietinalho,et al.  Effect of early vs late intervention with inhaled corticosteroids in asthma. , 1995, Chest.

[27]  S. Shire,et al.  Characterization of complex formation by humanized anti-IgE monoclonal antibody and monoclonal human IgE. , 1995, Biochemistry.

[28]  L. Presta,et al.  Inhibition of allergic reactions with antibodies to IgE. , 1995, International archives of allergy and immunology.

[29]  W. Morgan,et al.  Asthma and wheezing in the first six years of life. The Group Health Medical Associates. , 1995, The New England journal of medicine.

[30]  L. Presta,et al.  The binding site on human immunoglobulin E for its high affinity receptor. , 1994, The Journal of biological chemistry.

[31]  T. Haahtela,et al.  Effects of reducing or discontinuing inhaled budesonide in patients with mild asthma. , 1994, The New England journal of medicine.

[32]  S. Pedersen,et al.  Effects of long-term treatment with an inhaled corticosteroid on growth and pulmonary function in asthmatic children. , 1994, Respiratory medicine.

[33]  B. Zweiman The late-phase reaction: role of IgE, its receptor and cytokines. , 1993, Current opinion in immunology.

[34]  Alfred O. Berg,et al.  Clinical Guidelines And Primary Care Guidelines For The Diagnosis And Management Of Asthma , 2012 .

[35]  P. Turkeltaub,et al.  The association of individual allergen reactivity with respiratory disease in a national sample: data from the second National Health and Nutrition Examination Survey, 1976-80 (NHANES II). , 1992, The Journal of allergy and clinical immunology.

[36]  Turkeltaub Pc,et al.  Epidemiology of allergic disease and allergen skin test reactivity in the US population: data from the second National Health and Nutrition Examination Survey (1976-1980)-NHANES II. , 1992 .

[37]  P. Turkeltaub,et al.  Epidemiology of allergic disease and allergen skin test reactivity in the US population: data from the second National Health and Nutrition Examination Survey (1976-1980)-NHANES II. , 1992, Arbeiten aus dem Paul-Ehrlich-Institut (Bundesamt fur Sera und Impfstoffe) zu Frankfurt a.M.

[38]  S T Holgate,et al.  Exposure to house-dust mite allergen (Der p I) and the development of asthma in childhood. A prospective study. , 1990, The New England journal of medicine.

[39]  D. Postma,et al.  Prognosis of asthma from childhood to adulthood. , 1989, The American review of respiratory disease.

[40]  M. Chapman,et al.  Epidemiology of acute asthma: IgE antibodies to common inhalant allergens as a risk factor for emergency room visits. , 1989, The Journal of allergy and clinical immunology.

[41]  M. Kaliner,et al.  Late Phase Allergic Reactions , 1983, International journal of dermatology.

[42]  S. Wasserman Mediators of immediate hypersensitivity. , 1983, The Journal of allergy and clinical immunology.

[43]  N. Breslow,et al.  Statistical methods in cancer research: volume 1- The analysis of case-control studies , 1980 .

[44]  C. Pantin,et al.  Screening for IgE‐Mediated Allergy , 1980, Allergy.

[45]  E. Middleton,et al.  Allergy, principles and practice , 1978 .

[46]  M. Bazaral,et al.  Standardization and stability of immunoglobulin E (IgE). , 1972, The Journal of allergy and clinical immunology.

[47]  P. Elteren On the combination of independent two-sample tests of wilcoxon : Corrected version , 1959 .