Medical Genome Facility, Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Sci Rep. 2020 Jul 28;10(1):12584. doi: 10.1038/s41598-020-69358-4.
The relationship between primary biliary cholangitis (PBC), a chronic cholestatic autoimmune liver disease, and the peripheral immune system remains to be fully understood. Herein, we performed the first mass cytometry (CyTOF)-based, immunophenotyping analysis of the peripheral immune system in PBC at single-cell resolution. CyTOF was performed on peripheral blood mononuclear cells (PBMCs) from PBC patients (n = 33) and age-/sex-matched healthy controls (n = 33) to obtain immune cell abundance and marker expression profiles. Hierarchical clustering methods were applied to identify immune cell types and subsets significantly associated with PBC. Subsets of gamma-delta T cells (CD3TCRgd), CD8 T cells (CD3CD8CD161PD1), and memory B cells (CD3CD19CD20CD24CD27) were found to have lower abundance in PBC than in control. In contrast, higher abundance of subsets of monocytes and naïve B cells were observed in PBC compared to control. Furthermore, several naïve B cell (CD3CD19CD20CD24CD27) subsets were significantly higher in PBC patients with cirrhosis (indicative of late-stage disease) than in those without cirrhosis. Alternatively, subsets of memory B cells were lower in abundance in cirrhotic relative to non-cirrhotic PBC patients. Future immunophenotyping investigations could lead to better understanding of PBC pathogenesis and progression, and also to the discovery of novel biomarkers and treatment strategies.
原发性胆汁性胆管炎(PBC)是一种慢性胆汁淤积性自身免疫性肝病,其与外周免疫系统之间的关系尚未完全阐明。在此,我们首次在单细胞分辨率水平上,通过质谱流式细胞术(CyTOF)对 PBC 的外周免疫系统进行免疫表型分析。我们对 PBC 患者(n=33)和年龄/性别匹配的健康对照者(n=33)的外周血单个核细胞(PBMC)进行 CyTOF,以获得免疫细胞丰度和标志物表达谱。应用层次聚类方法鉴定与 PBC 显著相关的免疫细胞类型和亚群。γδ T 细胞(CD3TCRgd)、CD8 T 细胞(CD3CD8CD161PD1)和记忆 B 细胞(CD3CD19CD20CD27)的亚群在 PBC 患者中的丰度低于对照组。相比之下,PBC 患者中单核细胞和幼稚 B 细胞的亚群丰度高于对照组。此外,与无肝硬化的 PBC 患者相比,肝硬化(提示疾病晚期)患者的多个幼稚 B 细胞(CD3CD19CD20CD27)亚群显著更高。相反,在肝硬化与非肝硬化 PBC 患者相比,记忆 B 细胞的亚群丰度更低。未来的免疫表型研究可能会更好地理解 PBC 的发病机制和进展,并发现新的生物标志物和治疗策略。