MESOS:设计用于治疗哮喘的生物制剂的机制研究的考虑

C. Brightling, Millie Wang, M. Braddock, L. Nordenmark, Mattis Gottlow, G. Colice
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引用次数: 6

摘要

嗜酸性粒细胞是哮喘相关气道炎症和重塑的关键效应细胞;IL-13参与调节嗜酸性粒细胞活性。Tralokinumab是一种用于抑制IL-13的研究性全人源单克隆抗体,目前处于严重不受控制哮喘患者的III期临床开发阶段。在II期研究中,tralokinumab改善了那些IL-13轴上调的哮喘患者的肺功能,并具有其他临床益处。在接受定量计算机断层扫描的患者亚组中,气道形态测量学有所改善,提示可能对重塑有影响。II期MESOS研究(NCT02449473)旨在通过研究tralokinumab对嗜酸性粒细胞驱动的炎症和气道重塑的作用,更好地了解tralokinumab改善哮喘控制的作用机制。
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MESOS: considerations in designing a mechanistic study for a biologic used to treat asthma
Eosinophils are key effector cells in asthma-associated airway inflammation and remodeling; IL-13 is involved in regulating eosinophil activity. Tralokinumab, currently in Phase III clinical development for patients with severe uncontrolled asthma, is an investigational fully human monoclonal antibody designed to inhibit IL-13. In Phase II studies, tralokinumab improved lung function and had other clinical benefits in those patients with asthma who had an upregulated IL-13 axis. In a subgroup of patients that underwent quantitative computed tomography, there were improvements in airway morphometry, suggestive of a possible effect upon remodeling. The Phase II MESOS study (NCT02449473) aims to better understand the mechanism of action of tralokinumab in improving asthma control, by investigating tralokinumab effects on eosinophil-driven inflammation and airway remodeling.
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