The CSF in neurosarcoidosis contains consistent clonal expansion of CD8 T cells, but not CD4 T cells

被引:15
作者
Paley, Michael A. [1 ]
Baker, Brandi J. [2 ]
Dunham, S. Richard [2 ]
Linskey, Nicole [1 ]
Cantoni, Claudia [2 ]
Lee, Kenneth [2 ]
Hassman, Lynn M. [3 ]
Laurent, Jennifer [1 ]
Roberson, Elisha D. O. [1 ,4 ]
Clifford, David B. [2 ]
Yokoyama, Wayne M. [1 ]
机构
[1] Washington Univ, Dept Med, Sch Med, St Louis, MO 63110 USA
[2] Washington Univ, Dept Neurol, Sch Med, St Louis, MO 63110 USA
[3] Washington Univ, Dept Ophthalmol & Visual Sci, Sch Med, St Louis, MO 63110 USA
[4] Washington Univ, Dept Genet, Sch Med, St Louis, MO 63110 USA
基金
新加坡国家研究基金会;
关键词
Neurosarcoidosis; Sarcoidosis; T cells; TCR sequencing; Single-cell RNA sequencing; Interferon; PULMONARY SARCOIDOSIS; GENE USAGE; EBI2; MEMORY; LYMPHOCYTES; TOFACITINIB; MIGRATION; BLOOD; FLUID; FATE;
D O I
10.1016/j.jneuroim.2022.577860
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The tissue-specific drivers of neurosarcoidosis remain poorly defined. To identify cerebrospinal fluid (CSF) specific, antigen-driven T and B cell responses, we performed single-cell RNA sequencing of CSF and blood cells from neurosarcoid participants coupled to T and B cell receptor sequencing. In contrast to pulmonary sarcoidosis, which is driven by CD4 T cells, we found CD8 T cell clonal expansion enriched in the neurosarcoid CSF. These CSF-enriched CD8 T cells were composed of two subsets with differential expression of EBI2, CXCR3, and CXCR4. Lastly, our data suggest that IFN gamma signaling may distinguish neurosarcoidosis from other neurological disorders.
引用
收藏
页数:11
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