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外周血单细胞质量细胞术鉴定与原发性胆汁性胆管炎相关的免疫细胞亚群。

Single-cell mass cytometry on peripheral blood identifies immune cell subsets associated with primary biliary cholangitis.

机构信息

Medical Genome Facility, Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.

出版信息

Sci Rep. 2020 Jul 28;10(1):12584. doi: 10.1038/s41598-020-69358-4.

DOI:10.1038/s41598-020-69358-4
PMID:32724082
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7387528/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff1/7387528/f0f700c0b8a2/41598_2020_69358_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff1/7387528/271201fa455a/41598_2020_69358_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff1/7387528/d70280115f21/41598_2020_69358_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff1/7387528/a8436ac50919/41598_2020_69358_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff1/7387528/f0f700c0b8a2/41598_2020_69358_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff1/7387528/271201fa455a/41598_2020_69358_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff1/7387528/d70280115f21/41598_2020_69358_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff1/7387528/a8436ac50919/41598_2020_69358_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff1/7387528/f0f700c0b8a2/41598_2020_69358_Fig4_HTML.jpg

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