Walsh Garry M
a School of Medicine and Dentistry , University of Aberdeen , Scotland , UK.
Expert Rev Clin Immunol. 2017 Feb;13(2):143-149. doi: 10.1080/1744666X.2016.1216316. Epub 2016 Aug 2.
The development of monoclonal antibody-based biologics targeted at inhibition of the Th2 cytokines IL-4, IL-5 and IL-13 represent potentially effective treatments for patients with the glucocorticoid refractory eosinophilic asthma phenotype. Areas covered: Asthma exhibits marked heterogeneity both clinically and at the molecular phenotypic level, requiring specifically targeted treatments to block the key pathways of the disease. It is becoming apparent that significant clinical effects with anti-cytokine-based biologic therapies are more likely in carefully selected patient populations that take asthma phenotypes into account. The development of reproducible and straightforward discriminatory biomarkers may aid identification of those patients most likely to benefit from treatment with these expensive interventions. This narrative review is based on English-language original articles in PubMed or Med-Line that reported significant clinical findings published in the last two years on the evidence demonstrating the effectiveness or otherwise of the targeting of IL-4, IL-5, or IL-13 in carefully selected patients with severe refractory asthma. Expert commentary: The use of a baseline peripheral blood eosinophilia as a simple reproducible biomarker to identify patients with particular sub-phenotypes of asthma to guide the effective use of biologic therapy represents a significant step forward.
以抑制Th2细胞因子IL-4、IL-5和IL-13为靶点的基于单克隆抗体的生物制剂的研发,为糖皮质激素难治性嗜酸性粒细胞性哮喘表型患者提供了潜在的有效治疗方法。涵盖领域:哮喘在临床和分子表型水平上均表现出显著的异质性,需要针对性的治疗来阻断疾病的关键途径。越来越明显的是,在精心挑选、考虑了哮喘表型的患者群体中,基于抗细胞因子的生物疗法更有可能产生显著的临床效果。可重复且简单的鉴别生物标志物的研发,可能有助于识别那些最有可能从这些昂贵干预措施治疗中获益的患者。这篇叙述性综述基于PubMed或Med-Line上的英文原创文章,这些文章报道了过去两年发表的关于在精心挑选的重度难治性哮喘患者中靶向IL-4、IL-5或IL-13有效性证据的显著临床发现。专家评论:使用基线外周血嗜酸性粒细胞增多作为一种简单可重复的生物标志物,来识别具有特定哮喘亚表型的患者,以指导生物疗法的有效使用,这是向前迈出的重要一步。