靶向 COPD 中的 IL-5。

Targeting IL-5 in COPD.

机构信息

Section of Pulmonary, Critical Care and Sleep Medicine, Baylor College of Medicine, Houston, TX, USA.

出版信息

Int J Chron Obstruct Pulmon Dis. 2019 May 16;14:1045-1051. doi: 10.2147/COPD.S155306. eCollection 2019.

Abstract

Many patients with chronic obstructive pulmonary disease (COPD) continue to experience exacerbations despite receiving standard-of-care treatments. Novel approaches to COPD treatment focus on understanding and targeting molecular mechanisms of airway inflammation, airway obstruction, remodeling and lung destruction. Several identified phenotypes and endotypes of COPD will pave the future path for a more personalized approach to therapy. Although well known to be associated with neutrophilic inflammation, COPD may also be driven by eosinophilic inflammation both at stable states and during exacerbation. Targeting eosinophilic inflammation has been successful in managing severe eosinophilic asthma and may hold promise in certain phenotypes of COPD. The most promising biologic treatments at an advanced stage of development are agents blocking interleukin (IL)-5 or its receptor. This review examines our current understanding of the eosinophilic inflammation in COPD and the rationale for IL-5 targeting agents.

摘要

许多慢性阻塞性肺疾病(COPD)患者尽管接受了标准治疗,但仍会经历病情恶化。COPD 的新治疗方法侧重于了解和针对气道炎症、气道阻塞、重塑和肺破坏的分子机制。已经确定的 COPD 表型和内型将为更个性化的治疗方法铺平未来的道路。虽然众所周知与中性粒细胞炎症相关,但 COPD 在稳定期和恶化期也可能由嗜酸性粒细胞炎症驱动。靶向嗜酸性粒细胞炎症在管理严重嗜酸性哮喘方面已取得成功,并可能在 COPD 的某些表型中具有前景。在开发的后期阶段最有前途的生物治疗方法是阻断白细胞介素(IL)-5 或其受体的药物。本综述检查了我们对 COPD 中嗜酸性粒细胞炎症的现有理解以及针对 IL-5 靶向药物的基本原理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6867/6529620/dfcdc9459ed4/COPD-14-1045-g0001.jpg

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