Treating Moderate-to-Severe Allergic Asthma with a Recombinant Humanized Anti-IgE Monoclonal Antibody (Omalizumab).

Gennaro D'Amato, Enrica Bucchioni, Virginio Oldani, Walter Canonica
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引用次数: 17

Abstract

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.

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重组人源化抗ige单克隆抗体(Omalizumab)治疗中重度过敏性哮喘。
支气管哮喘是一种呼吸道慢性炎症性疾病,在发达国家和发展中国家都被认为是一种非常普遍的健康问题,具有重大的人类和经济后果。过敏被认为是哮喘的主要危险因素。过敏性哮喘的发病特点是气道炎症,肥大细胞、嗜碱性粒细胞、嗜酸性粒细胞、单核细胞和辅助T型2淋巴细胞浸润,同时B细胞的同型转换产生免疫球蛋白E (IgE)类免疫球蛋白。哮喘严重程度的增加不仅与反复住院和死亡率增加有关,而且还与更高的社会成本有关。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,但仍有相当数量的哮喘患者在接受吸入性糖皮质激素和长效β(2)-肾上腺素受体激动剂(β(2)-激动剂)治疗后仍有症状,有时需要全身性糖皮质激素来控制病情。这些患者约占哮喘医疗费用的50%。因此,这些患者需要新的治疗方案,更具体地针对引起哮喘发展的病理生理事件。一种新的治疗哮喘和其他过敏性呼吸系统疾病的方法涉及干扰IgE的作用和预防随后的IgE介导反应。Omalizumab是一种人源化重组单克隆抗ige抗体,用于治疗过敏性疾病,对青少年和成人中重度过敏性哮喘患者有明显疗效。这种非过敏性抗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。Omalizumab治疗耐受性良好,可显著改善症状和疾病控制,减少哮喘加重和使用大剂量吸入皮质类固醇的需要。此外,omalizumab改善了严重持续性过敏性哮喘患者的生活质量,这些患者目前可用的哮喘药物无法充分控制。总之,对于吸入皮质类固醇+ β(2)-激动剂控制不充分的中重度哮喘患者,omalizumab可能满足其重要需求。
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