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Tralokinumab, an anti-IL-13 mAb for the potential treatment of asthma and COPD

机译:Tralokinumab,一种抗IL-13 mAb,可潜在治疗哮喘和COPD

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摘要

Biopharmaceutical approaches have been used to target key elements in the processes controlling airway inflammation in asthma and COPD. There is compelling evidence that IL-13 is a key mediator in the inflammatory processes in the asthmatic lung. Tralokinumab (CAT-354), under development by MedImmune, is an injectable, anti-IL-13 humanized mAb for the potential treatment of asthma and COPD. In a study in mice, tralokinumab prevented the development of the asthmatic phenotype, including eosinophil recruitment and airway hyperresponsiveness. In clinical trials, tralokinumab demonstrated favorable safety and pharmacokinetic profiles, both in healthy volunteers and in patients with asthma. This review summarizes the problems and successes regarding recent developments in mAb-based strategies targeted against IL-13 in asthma and COPD, with an emphasis on tralokinumab.
机译:在控制哮喘和COPD中气道炎症的过程中,已使用生物药物方法来靶向关键要素。有令人信服的证据表明,IL-13是哮喘肺炎症过程中的关键介质。 Tralokinumab(CAT-354)由MedImmune开发,是一种可注射的抗IL-13人源化mAb,可用于治疗哮喘和COPD。在小鼠的一项研究中,曲妥珠单抗阻止了哮喘表型的发展,包括嗜酸性粒细胞募集和气道高反应性。在临床试验中,无论是在健康志愿者中还是在哮喘患者中,tralokinumab均显示出良好的安全性和药代动力学特征。这篇综述总结了针对针对哮喘和COPD中IL-13的基于mAb的策略的最新进展所面临的问题和成功,重点是曲妥单抗。

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