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Mepolizumab in the management of severe eosinophilic asthma in adults: current evidence and practical experience

机译:Mepolizumab在成人中严重嗜酸性哮喘管理:当前的证据和实践经验

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Asthma is a chronic inflammatory condition involving the airways with varying pathophysiological mechanisms, clinical symptoms and outcomes, generally controlled by conventional therapies including inhaled corticosteroids and long-acting beta(2) agonists. However, these therapies are unable to successfully control symptoms in about 5-10% of severe asthma patients. Atopic asthma, characterized by high immunoglobulin (Ig) E or eosinophilia, represents about 50% of asthmatic patients. Interleukin (IL)-5 is the main cytokine responsible of activation of eosinophils, hence therapeutic strategies have been investigated and developed for clinical use. Biologics targeting IL-5 and its receptor (first mepolizumab and subsequently, reslizumab and benralizumab), have been recently approved and used as add-on therapy for severe eosinophilic asthma resulting in a reduction in the circulating eosinophil count, improvement in lung function and exacerbation reduction in asthma patients. Despite these biologics having been approved for stratified severe asthma patients that remain uncontrolled with high doses of conventional therapy, a number of patients may be eligible for more than one biologic. Presently, the lack of head-to-head studies comparing the biological agents among themselves and with conventional therapy make the choice of optimal therapy for each patient a challenge for clinicians. Moreover, discontinuation of these treatments, implications for efficacy or adverse events, in particular in long-term treatment, and needs for useful biomarkers are still matters of debate. In this review we evaluate to date, the evidence on mepolizumab that seems to demonstrate it is a well-tolerated and efficacious regimen for use in severe eosinophilic asthma, though more studies are still required.
机译:哮喘是一种慢性炎症病症,涉及气道,具有不同的病理生理机制,临床症状和结果,通常由常规疗法控制,包括吸入的皮质类固醇和长效β(2)激动剂。然而,这些疗法无法成功地控制哮喘严重哮喘患者约5-10%的症状。特征在于高免疫球蛋白(IG)E或嗜酸性粒细胞素的特征性哮喘,占哮喘患者的约50%。白细胞介素(IL)-5是负责嗜酸性粒细胞活化的主要细胞因子,因此对临床用途进行了研究和开发治疗策略。靶向IL-5及其受体(首发Mepolizumab和随后,Reslizumab和Benralizumab)的生物制剂已被批准并用作严重的嗜酸性嗜型哮喘的附加治疗,导致循环嗜酸性粒细胞计数降低,肺功能提高和加剧减少哮喘患者。尽管已经批准了这些生物学,但已经批准了已经用高剂量的常规治疗不受控制的分层严重的哮喘患者,许多患者可能有资格获得多种生物学。目前,缺乏头脑研究,比较自己和常规治疗的生物药物,使每人患者对临床医生的挑战进行最佳治疗。此外,停止这些治疗,对疗效或不良事件的影响,特别是在长期治疗中,对有用的生物标志物的需求仍然是辩论的重要事项。在这篇评论中,我们评估迄今为止,似乎证明它是在严重的嗜酸性哮喘中使用良好和有效的方案,但仍然需要更多的研究。

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