D'Amato Gennaro, Stanziola Anna, Sanduzzi Alessandro, Liccardi Gennaro, Salzillo Antonello, Vitale Carolina, Molino Antonio, Vatrella Alessandro, D'Amato Maria
Division of Respiratory and Allergic Diseases, Department of Respiratory Diseases, High Speciality Hospital A. Cardarelli, Naples, Italy ; Committee of Ministry of Health on "Pollution, Climate and Respiratory Health, Naples, Italy ; Chairman Committee and Task Force on "Air pollution, climate change and allergic respiratory diseases" World Allergy Organization, Naples, Italy.
Division of Pneumology, Department of Respiratory Diseases, High Speciality Hospital "V.Monaldi" Naples and University of Naples Federico II, Naples, Italy.
Multidiscip Respir Med. 2014 Apr 15;9(1):23. doi: 10.1186/2049-6958-9-23. eCollection 2014.
Increased asthma severity is not only associated with enhanced recurrent hospitalization and mortality but also with higher social costs. Several cases of asthma are atopic in nature, with the trigger for acute asthma attacks and chronic worsening of inflammation being allergens inducing an immune, IgE mediated response. Anti-inflammatory treatments are effective for most of asthma patients, but there are subjects whose disease is incompletely controlled by inhaled or systemic corticosteroids and these patients account for about 50% of the healthcare costs of asthma. Omalizumab is a biological engineered, humanized recombinant monoclonal anti-IgE antibody developed for the treatment of allergic diseases and with clear efficacy in adolescent and adult patients with severe allergic asthma. The anti-IgE antibody inhibits IgE functions blocking free serum IgE and inhibiting their binding to cellular receptors. By reducing serum IgE levels and IgE receptor expression on inflammatory cells in the context of allergic cascade, omalizumab has demonstrated to be a very useful treatment of atopic asthma, improving quality of life of patients with severe persistent allergic asthma that is inadequately controlled by currently available asthma medications. Several trials have demonstrated that this therapy is well tolerated and significantly improves symptoms and disease control, reducing asthma exacerbations and the need to use high dosage of inhaled corticosteroids.
哮喘严重程度增加不仅与反复住院率和死亡率升高相关,还与更高的社会成本相关。几例哮喘本质上是特应性的,急性哮喘发作和炎症慢性恶化的触发因素是诱导免疫性IgE介导反应的过敏原。抗炎治疗对大多数哮喘患者有效,但有些患者的疾病不能通过吸入或全身用皮质类固醇得到完全控制,这些患者占哮喘医疗费用的约50%。奥马珠单抗是一种生物工程的人源化重组单克隆抗IgE抗体,开发用于治疗过敏性疾病,对重度过敏性哮喘的青少年和成年患者有明确疗效。抗IgE抗体抑制IgE功能,阻断游离血清IgE并抑制其与细胞受体的结合。通过在过敏级联反应中降低血清IgE水平和炎症细胞上的IgE受体表达,奥马珠单抗已被证明是治疗特应性哮喘的非常有用的药物,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。几项试验表明,这种疗法耐受性良好,可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皮质类固醇的需求。