Goss Kyndal, Grant Melanie L, Caldwell Cherish, Dallalio Gail A, Stephenson Susan T, Fitzpatrick Anne M, Horwitz Edwin M
Marcus Center for Advanced Cellular Therapy, Atlanta, GA, USA.
Aflac Cancer & Blood Disorders Center, Atlanta, GA, USA.
iScience. 2025 May 26;28(6):112609. doi: 10.1016/j.isci.2025.112609. eCollection 2025 Jun 20.
Asthma is the most common chronic lung disorder in the United States. While asthma is heterogeneous, blood eosinophils are central to the pathogenesis in most cases. Yet, the power of modern omics has not been widely applied to the study of asthma eosinophils. We report single cell RNA sequencing of blood eosinophils obtained from patients with severe asthma, mild asthma, and healthy volunteers. The eosinophils from asthma patients showed marked heterogeneity in the population and, as with healthy controls, clustered into 3 subsets suggesting at least 3 gene expression states circulating in the blood. Eosinophils from asthma patients had an inflammatory gene signature with enrichment of interferon α and γ pathways. Moreover, a greater fraction of these eosinophils expressed CCR3, the chemokine receptor that mediates trafficking to inflamed tissues and activates eosinophils. Our data support implementation of larger studies to define the transcriptional drivers of asthma.
哮喘是美国最常见的慢性肺部疾病。虽然哮喘具有异质性,但在大多数情况下,血液嗜酸性粒细胞是发病机制的核心。然而,现代组学技术尚未广泛应用于哮喘嗜酸性粒细胞的研究。我们报告了从重度哮喘患者、轻度哮喘患者和健康志愿者中获取的血液嗜酸性粒细胞的单细胞RNA测序结果。哮喘患者的嗜酸性粒细胞在群体中表现出明显的异质性,并且与健康对照一样,聚集成3个亚群,表明血液中至少存在3种基因表达状态。哮喘患者的嗜酸性粒细胞具有炎症基因特征,其中干扰素α和γ途径富集。此外,这些嗜酸性粒细胞中有更大比例表达CCR3,这是一种趋化因子受体,介导向炎症组织的转运并激活嗜酸性粒细胞。我们的数据支持开展更大规模的研究来确定哮喘的转录驱动因素。