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Editorial: Pathogenic Advances and Therapeutic Perspectives for Eosinophilic Inflammation

机译:社论:嗜酸性粒细胞炎症的病因学进展和治疗前景

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With the recent approval of the first eosinophil-depleting therapeutic agents targeting the Interleukin-5 (IL-5) pathway for treatment of severe eosinophilic asthma, eosinophils, and eosinophilic disorders are in the limelight. Setbacks during clinical development of these compounds have revealed how much remains to be known about eosinophil biology in vivo, and have nurtured profuse research both on basic eosinophil biology and on pathogenic disease mechanisms, in order to better delineate the most meaningful targets for innovative therapeutic strategies. On one hand, variable degrees of eosinophil depletion observed in some compartments during IL-5-targeted treatment indicate that certain eosinophil subsets may not rely on this cytokine and/or that other important pro-eosinophilic mediators and signaling pathways are operative in vivo. On the other hand, it is increasingly clear that disorders involving eosinophils such as asthma are the final outcome of complex interactions between diverse cell types and mediators, beyond eosinophils and IL-5. These include type 2 helper T (Th2) cells and innate lymphoid cells, mast cells, and a variety of factors that either activate eosinophils or are released by them. Although a considerable amount of research has focused on asthma because it is a common condition and because management of severe asthma remains a major challenge, several rare eosinophilic disorders with more homogenous features have proven to be extremely useful models to reach a better understanding of the involvement of eosinophils in tissue damage and dysfunction, and of the micro-environmental interactions operating within the complex network of eosinophilic inflammation. Unraveling this interplay has resulted in advances in the development of molecular tools to detect disease subsets and to monitor therapeutic responses, and in identification of promising new therapeutic targets. Precision medicine for management of eosinophilic disorders has now become a realistic endeavor.
机译:最近,针对白细胞介素5(IL-5)途径的首个用于治疗严重嗜酸性粒细胞性哮喘的嗜酸性粒细胞减少治疗剂,嗜酸性粒细胞和嗜酸性粒细胞疾病备受关注。这些化合物的临床开发过程中的挫折揭示了体内关于嗜酸性粒细胞生物学尚待了解的知识,并培育了有关嗜酸性粒细胞基础生物学和病原性疾病机制的大量研究,以便更好地描绘出创新治疗策略中最有意义的目标。一方面,在靶向IL-5的治疗过程中在某些隔室中观察到的嗜酸性粒细胞耗竭程度不同,这表明某些嗜酸性粒细胞亚群可能不依赖该细胞因子和/或其他重要的嗜酸性粒细胞亲和介质和信号通路在体内起作用。另一方面,越来越明显的是,涉及嗜酸性粒细胞的疾病(例如哮喘)是嗜酸性粒细胞和IL-5以外的各种细胞类型与介体之间复杂相互作用的最终结果。这些包括2型辅助性T(Th2)细胞和先天性淋巴样细胞,肥大细胞,以及激活嗜酸性粒细胞或由其释放的多种因素。尽管由于哮喘是一种常见病,并且因为应对重症哮喘仍然是一项重大挑战,所以针对哮喘的研究已经很多,但是事实证明,一些罕见的嗜酸性粒细胞疾病具有更均一的特征,对于更好地了解哮喘的发生是非常有用的模型。嗜酸性粒细胞在组织损伤和功能障碍中的作用,以及在嗜酸性粒细胞炎症的复杂网络中起作用的微环境相互作用。阐明这种相互作用已导致开发用于检测疾病亚型和监测治疗反应以及鉴定有希望的新治疗靶标的分子工具。现在,用于治疗嗜酸性粒细胞疾病的精密药物已成为现实。

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