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Anti-IL-5 Biologicals Targeting Severe Late Onset Eosinophilic Asthma

机译:针对重度迟发性嗜酸性哮喘的抗IL-5生物学药物

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摘要

Improved knowledge about the pathogenesis of asthma has facilitated the development of novel drugs and provided hope for patients with severe asthma. After the short- and long-term success of omalizumab in severe allergic phenotype, researchers have targeted patients with severe eosinophilic asthma who comprise up to 45% of adult severe asthma. Interleukin (IL)-5 and IL-5 receptor subunit α play crucial roles in the development, maturation, and operation of eosinophils. Currently, patients treated with anti-IL-5 biologicals depleting eosinophils experience the positive efficacy of these drugs, especially with regard to the reduction of exacerbation rate. The aim of this review was to shed light on severe eosinophilic asthma treatment with these new currently available agents selectively targeting IL-5 or its receptor, discussing their usage including pre-treatment concerns, such as selecting the target population and choosing the right agent among them, and subsequent assessment of relevant effect and safety issues.
机译:对哮喘发病机理的认识的提高促进了新药的开发,并为重症哮喘患者提供了希望。 omalizumab在严重过敏表型上短期和长期成功之后,研究人员针对了严重嗜酸性粒细胞性哮喘的患者,这些患者占成人严重哮喘的45%。白细胞介素(IL)-5和IL-5受体亚基α在嗜酸性粒细胞的发育,成熟和运作中起着至关重要的作用。当前,用抗IL-5生物学耗竭性嗜酸性粒细胞治疗的患者经历了这些药物的积极疗效,尤其是在恶化率降低方面。这篇综述的目的是阐明使用这些新的目前可用的选择性靶向IL-5或其受体的新药物对严重嗜酸性哮喘的治疗方法,讨论其用途,包括治疗前的顾虑,例如选择目标人群并在其中选择合适的药物它们,以及随后对相关影响和安全问题的评估。

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