杜皮鲁玛
嗜酸性粒细胞增多症
嗜酸性粒细胞
苯拉唑马布
免疫学
医学
免疫疗法
生物标志物
白细胞介素5
过敏
美波利祖马布
细胞因子
免疫系统
哮喘
生物
白细胞介素
生物化学
作者
Joseph Cafone,Melanie A. Ruffner,Jonathan M. Spergel
标识
DOI:10.1007/s11882-020-0895-x
摘要
The purpose of this review is to provide a brief discussion on the differential diagnosis for peripheral eosinophilia. We will then focus on targeted immunotherapies for atopic disease, their effects on absolute peripheral eosinophil counts, and use of peripheral eosinophils as a predictor of treatment response.In atopic disease, lower absolute peripheral eosinophil counts are typically associated with improved outcomes. Much of the current evidence on eosinophils as a biomarker comes from post hoc analyses in therapeutic immunotherapy. While changes in eosinophilia were not the primary outcome of interest in many studies, some patterns did emerge. Cytolytic monoclonal antibodies AK002 and benralizumab completely reduce peripheral and tissue eosinophil numbers. Dupilumab may have paradoxical transient eosinophilia despite observed clinical efficacy. Atopic inflammation is complex largely due to the various cytokines which affect eosinophil activation, proliferation, differentiation, and survival. This demonstrates the challenges of using peripheral eosinophilia alone as a biomarker for atopic disease activity. More attention should spotlight how different immunotherapy modalities affect eosinophil-driven responses.
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