D'Amato Gennaro, Bucchioni Enrica, Oldani Virginio, Canonica Walter
Division of Respiratory and Allergic Diseases, Department of Respiratory Diseases, High Speciality Hospital A. Cardarelli, Naples, Italy.
Treat Respir Med. 2006;5(6):393-8. doi: 10.2165/00151829-200605060-00004.
Bronchial asthma is a chronic inflammatory disease of the airways which is recognized as a highly prevalent health problem in both the developed and the developing world, with significant human and economic consequences.Allergy is acknowledged as a major risk factor for asthma. The pathogenetic aspects of allergic asthma are characterized by airway inflammation with infiltration of mast cells, basophils, eosinophils, monocytes and T helper type 2 lymphocytes, along with the isotype switching of B cells to generate immunoglobulins of the immunoglobulin E (IgE) class. Increased asthma severity is not only associated with recurrent hospitalization and increased mortality but also with higher social costs.Inhaled corticosteroids are the standard anti-inflammatory medication and are effective for most asthma patients, but there is a substantial number of asthmatics who remain symptomatic even after receiving treatment with inhaled corticosteroids and long-acting beta(2)-adrenoceptor agonists (beta(2)-agonists), and sometimes are in need of systemic corticosteroids to control the disease. These patients account for about 50% of the healthcare costs of asthma.New treatment options more specifically targeting the pathophysiologic events causing development of asthma are therefore required in these patients.A novel therapeutic approach to asthma and other allergic respiratory diseases involves interference with the action of IgE and prevention of subsequent IgE-mediated responses.Omalizumab is a humanized recombinant monoclonal anti-IgE antibody developed for the treatment of allergic diseases, with clear efficacy in adolescent and adult patients with moderate-to-severe allergic asthma. This non-anaphylactogenic anti-IgE antibody inhibits IgE functions by blocking free serum IgE and inhibiting their binding to cellular receptors. Omalizumab therapy is well tolerated and significantly improves symptoms and disease control, and reduces asthma exacerbations and the need to use high dosages of inhaled corticosteroids. Moreover, omalizumab improves quality of life of patients with severe persistent allergic asthma that is inadequately controlled by currently available asthma medications. In conclusion, omalizumab may fulfill an important need in patients with moderate-to-severe asthma inadequately controlled with inhaled corticosteroids +beta(2)-agonists.
支气管哮喘是一种气道慢性炎症性疾病,在发达国家和发展中国家均被视为一个高度普遍的健康问题,会造成重大的人力和经济后果。过敏被公认为哮喘的主要危险因素。过敏性哮喘的发病机制特点是气道炎症,伴有肥大细胞、嗜碱性粒细胞、嗜酸性粒细胞、单核细胞和2型辅助性T淋巴细胞浸润,同时B细胞发生同种型转换以产生免疫球蛋白E(IgE)类免疫球蛋白。哮喘严重程度增加不仅与反复住院和死亡率上升有关,还与更高的社会成本相关。吸入性糖皮质激素是标准的抗炎药物,对大多数哮喘患者有效,但有相当一部分哮喘患者即使接受吸入性糖皮质激素和长效β2肾上腺素能受体激动剂(β2激动剂)治疗后仍有症状,有时还需要全身使用糖皮质激素来控制病情。这些患者占哮喘医疗费用的约50%。因此,这些患者需要更有针对性地针对导致哮喘发生的病理生理事件的新治疗选择。一种针对哮喘和其他过敏性呼吸道疾病的新型治疗方法涉及干扰IgE的作用并预防随后的IgE介导的反应。奥马珠单抗是一种为治疗过敏性疾病而研发的人源化重组单克隆抗IgE抗体,对中度至重度过敏性哮喘的青少年和成年患者有明确疗效。这种非致过敏性抗IgE抗体通过阻断游离血清IgE并抑制其与细胞受体的结合来抑制IgE功能。奥马珠单抗治疗耐受性良好,能显著改善症状和疾病控制,减少哮喘发作以及使用高剂量吸入性糖皮质激素的需求。此外,奥马珠单抗可改善目前可用哮喘药物控制不佳的重度持续性过敏性哮喘患者的生活质量。总之,奥马珠单抗可能满足那些使用吸入性糖皮质激素+β2激动剂控制不佳的中度至重度哮喘患者的重要需求。