Mechanisms, diagnosis and management of eosinophilic asthma

N. Syabbalo
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引用次数: 1

Abstract

Asthma is a common chronic airway disease affecting about 334 million people worldwide, and up to 10% of asthma patients have severe asthma, which may be uncontrolled despite high doses of the standard treatment modifiers and may require the use of chronic oral corticosteroids. It is the most common chronic disease in children in the developed countries. Asthmamanifests as reversible airflow obstruction, due to airway inflammation, bronchial smooth muscle contraction, increased mucus secretion, vascular engorgement, mucosal oedema, and airway hyper responsiveness, which leads to airflow obstruction and symptoms of asthma. Eosinophilic asthma is a phenotype of asthma that is usually very severe and persistent, with frequent exacerbations. It is usually observed in adult asthmatic patients, although it may occur in children. It is characterized by the presence of high levels of eosinophils, and CD+4 Th2 cells in the lungs and airways, which can be demonstrated by a raised eosinophil count in blood, and induced sputum or bronchial biopsy. It is managed in a similar stepwise treatment for childhood-onset asthma, but some of the patients with eosinophilic asthma do not respond to this standard treatment including inhaled or oral corticosteroids. The logical approach to treat corticosteroid-refractory asthma is to target the eosinophilic interleukins which cause airway inflammation using monoclonal antibodies to block their activity on the eosinophils, and Th2 cells. Currently, the following monoclonal antibodies are used in the treatment of eosinophilic asthma: IgE antibody such as omalizumab, or interleukin receptor 5, or 4, and 13 antagonists, such mepolizumab, reslizumab, and dupilumab. These novel agents have proved to be very useful in relieving the symptoms, and in improving the forced expired volume in one second (FEV1), and in reducing exacerbations. They are also steroid-sparing agents, and improve the quality of lifein this debilitating phenotype of asthma.
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嗜酸性粒细胞哮喘的发病机制、诊断和治疗
哮喘是一种常见的慢性气道疾病,影响全球约3.34亿人,高达10%的哮喘患者患有严重哮喘,尽管使用高剂量的标准治疗调节剂,但哮喘可能无法控制,可能需要使用慢性口服皮质类固醇。这是发达国家儿童中最常见的慢性疾病。哮喘表现为可逆性气流阻塞,气道炎症、支气管平滑肌收缩、粘液分泌增加、血管充血、粘膜水肿、气道反应性亢进,导致气流阻塞,出现哮喘症状。嗜酸性哮喘是哮喘的一种表型,通常是非常严重和持续的,经常恶化。它通常见于成人哮喘患者,但也可能发生在儿童身上。其特征是肺和气道中存在高水平的嗜酸性粒细胞和CD+4 Th2细胞,这可以通过血液中嗜酸性粒细胞计数升高、诱导痰或支气管活检来证明。这是一种类似的儿童期发作哮喘的分步治疗,但一些嗜酸性哮喘患者对这种标准治疗(包括吸入或口服皮质类固醇)没有反应。治疗皮质类固醇难治性哮喘的合理方法是使用单克隆抗体靶向引起气道炎症的嗜酸性白细胞介素,以阻断其对嗜酸性粒细胞和Th2细胞的活性。目前,以下单克隆抗体用于治疗嗜酸性粒细胞哮喘:IgE抗体,如omalizumab,或白细胞介素受体5或4,以及13拮抗剂,如mepolizumab, reslizumab和dupilumab。这些新型药物已被证明在缓解症状、提高一秒内强制呼气容积(FEV1)和减少恶化方面非常有用。它们也是类固醇节省剂,并改善生活质量在这种衰弱的哮喘表型。
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