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生物制剂在重度哮喘治疗中的应用

Biologics in the treatment of severe asthma.

作者信息

Quirce S, Phillips-Angles E, Domínguez-Ortega J, Barranco P

机构信息

Department of Allergy, Hospital La Paz Institute for Health Research (IdiPAZ), Madrid, Spain; CIBER de Enfermedades Respiratorias, CIBERES, Spain.

Department of Allergy, Hospital Universitario La Paz, Madrid, Spain.

出版信息

Allergol Immunopathol (Madr). 2017 Dec;45 Suppl 1:45-49. doi: 10.1016/j.aller.2017.09.012. Epub 2017 Nov 3.

DOI:10.1016/j.aller.2017.09.012
PMID:29108767
Abstract

Severe asthma is defined as asthma which requires treatment with high dose inhaled corticosteroids and with a second controller drug to prevent it from becoming uncontrolled or which remains uncontrolled despite this therapy. Patients with uncontrolled severe asthma require additional treatment options as add-on therapy, including biologics. Biologic therapies in asthma are designed to block key immune regulators, such as IgE, or certain pro-inflammatory cytokines, e.g. interleukin (IL)-5, IL-4, IL-13 or IL-17. Patients with severe asthma and eosinophilic phenotype may benefit from biologic therapies aimed at reducing blood and tissue eosinophils, such as mepolizumab, reslizumab and benralizumab. Patients with Th2-high phenotype may also benefit from therapy with anti-IL-4/anti-IL-13 monoclonal antibodies (dupilumab). The main limitations of asthma treatment with biologic agents are the crossover and overlap of the different pathways in the pathogenesis of asthma which may cause lack of complete success of these therapies, in addition of high costs, which make pharmacoeconomic studies necessary to identify the ideal target patient population to receive these biologic drugs.

摘要

重度哮喘被定义为需要使用高剂量吸入性糖皮质激素和第二种控制药物进行治疗以防止病情失控,或尽管进行了这种治疗仍未得到控制的哮喘。未得到控制的重度哮喘患者需要额外的治疗选择作为附加疗法,包括生物制剂。哮喘的生物疗法旨在阻断关键的免疫调节因子,如IgE,或某些促炎细胞因子,如白细胞介素(IL)-5、IL-4、IL-13或IL-17。重度哮喘和嗜酸性粒细胞表型的患者可能受益于旨在减少血液和组织嗜酸性粒细胞的生物疗法,如美泊利单抗、瑞利珠单抗和贝那利珠单抗。Th2高表型的患者也可能受益于抗IL-4/抗IL-13单克隆抗体(度普利尤单抗)治疗。使用生物制剂治疗哮喘的主要局限性在于哮喘发病机制中不同途径的交叉和重叠,这可能导致这些疗法无法完全成功,此外成本高昂,这使得有必要进行药物经济学研究以确定接受这些生物药物的理想目标患者群体。

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