脑脊液
多发性硬化
表型
免疫学
生物
细胞毒性T细胞
免疫系统
转录组
中枢神经系统
髓样
细胞
神经科学
体外
基因
基因表达
生物化学
遗传学
作者
David Schafflick,Chenling Xu,Maike Hartlehnert,Michael B. Cole,Tobias Lautwein,Andreas Schulte‐Mecklenbeck,Jolien Wolbert,Michael Heming,Sven G. Meuth,Tanja Kuhlmann,Catharina C. Groß,Heinz Wiendl,Nir Yosef,Gerd Meyer zu Hörste
摘要
Summary Cerebrospinal fluid (CSF) protects the central nervous system (CNS) and analyzing CSF aids the diagnosis of CNS diseases, but our understanding of CSF leukocytes remains superficial. Here, we firstly provide a transcriptional map of single leukocytes in CSF compared to blood. Leukocyte composition and transcriptome were compartment-specific with CSF-enrichment of myeloid dendritic cells and a border-associated phenotype of monocytes. We secondly tested how multiple sclerosis (MS) - an autoimmune disease of the CNS - affected both compartments. MS increased transcriptional diversity in blood, while it preferentially increased cell type diversity in CSF. In addition to the known expansion of B lineage cells, we identified an increase of cytotoxic-phenotype and follicular T helper (TFH) cells in the CSF. In mice, TFH cells accordingly promoted B cell infiltration into the CNS and severity of MS animal models. Immune mechanisms in MS are thus highly compartmentalized and indicate local T/B cell interaction.
科研通智能强力驱动
Strongly Powered by AbleSci AI