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Survey of Opinion of Spanish Physicians on the Role of Eosinophils in Asthma and Other Diseases

机译:西班牙医师关于嗜酸性粒细胞在哮喘和其他疾病中作用的观点调查

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摘要

Eosinophilic asthma is the most common inflammatory phenotype, accounting for over 25% of all patients with severe asthma. It is characterized by abnormal production of cytokines from type 2 helper T lymphocytes and type 2 innate lymphoid cells (ILC-2s), such as IL-4, IL-5, and IL-13, as well as a persistent increase and activation of eosinophils in blood and airways despite treatment with high-dose corticosteroids [1,2]. Blood and sputum eosinophilia are associated with more severe disease, poorer control, and worse prognosis [3]. The most direct way to diagnose severe eosinophilic asthma is through diagnosis of severe asthma, which is characterized by ≥2 exacerbations per year, dependence on oral corticosteroids to achieve asthma control, and a persistent increase in the eosinophil count in blood and the airways [2]. Eosinophils represent approximately 1% of peripheral blood leukocytes, and their differentiation, survival, and activation are regulated mainly by IL-5 [4]. Irrespective of the presence of allergy, severe, uncontrolled eosinophilic asthma is treated with biological drugs that target either eosinophils or the IL-5 pathway. On the one hand, biologic therapies targeting eosinophils include drugs blocking eosinophil recruitment, such as bertilimumab, which prevents accumulation of these cells in tissues [5]. On the other hand, drugs targeting the IL-5 pathway may be used, either directly against IL-5 (mepolizumab and reslizumab) or the IL-5 receptor (IL-5R a ) (benralizumab) [6-9]. By blocking the interaction between IL-5 and its receptor, the eosinophil count in blood and the airway decreases, as does survival of these cells, thus decreasing the symptoms of the disease. Another treatment approach includes inhibition of IL-4R a by blocking the action of IL-4 and IL-13. This strategy prevents the stimulation of type 2 inflammation, which contributes to asthma. Dupilumab is a monoclonal antibody targeting IL-R4 a? [10]. It was recently approved by the United States Food and Drug Administration for the treatment of moderate and severe asthma in patients with the eosinophilic phenotype.
机译:嗜酸性哮喘是最常见的炎症表型,占所有严重哮喘患者的25%以上。它的特征是从2型辅助T淋巴细胞和2型先天性淋巴样细胞(ILC-2),例如IL-4,IL-5和IL-13异常产生细胞因子,以及持续增加和激活细胞因子。尽管用大剂量皮质类固醇治疗,血液和呼吸道中的嗜酸性粒细胞[1,2]。血液和痰嗜酸性粒细胞增多与疾病更严重,控制更差和预后更差有关[3]。诊断严重嗜酸性粒细胞性哮喘最直接的方法是通过诊断严重哮喘,其特征是每年≥2次加重,依赖口服皮质类固醇来控制哮喘,以及血液和呼吸道中嗜酸性粒细胞数量持续增加[2] ]。嗜酸性粒细胞约占外周血白细胞的1%,其分化,存活和激活主要受IL-5调节[4]。无论是否存在过敏,都可以使用针对嗜酸性粒细胞或IL-5途径的生物药物治疗严重,不受控制的嗜酸性哮喘。一方面,针对嗜酸性粒细胞的生物疗法包括阻止嗜酸性粒细胞募集的药物,例如bertilimumab,它阻止了这些细胞在组织中的积累[5]。另一方面,可以使用靶向IL-5途径的药物,直接针对IL-5(Mepolizumab和Reslizumab)或IL-5受体(IL-5R a)(贝那珠单抗)[6-9]。通过阻断IL-5与其受体之间的相互作用,血液和气道中的嗜酸性粒细胞数量减少,这些细胞的存活也减少,从而减轻了疾病的症状。另一种治疗方法包括通过阻断IL-4和IL-13的作用来抑制IL-4R a。该策略可防止刺激导致哮喘的2型炎症。 Dupilumab是针对IL-R4α的单克隆抗体吗? [10]。最近,它被美国食品和药物管理局批准用于治疗嗜酸性表型患者的中度和重度哮喘。

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