Type 1 innate lymphoid cells: a biomarker and therapeutic candidate in sarcoidosis

被引:1
|
作者
Cho, Inchul [1 ,2 ]
Ji, Andrew L. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Dermatol, New York, NY USA
[2] Icahn Sch Med Mt Sinai, Black Family Stem Cell Inst, New York, NY USA
[3] Icahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY USA
[4] Icahn Sch Med Mt Sinai, Dept Cell Dev & Regenerat Biol, New York, NY USA
[5] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 2024年 / 134卷 / 17期
关键词
EXPRESSION; CXCR4;
D O I
10.1172/JCI183708
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Sarcoidosis is an inflammatory disease characterized by immune cell-rich granulomas that form in multiple organs. In this issue of the JCI, , Sati and colleagues used scRNA-seq and spatial transcriptomics of skin samples from patients with sarcoidosis and non-sarcoidosis granulomatous disease to identify upregulation of a stromal-immune CXCL12/CXCR4 axis and accumulation of type 1 innate lymphoid cells (ILC1s) in sarcoidosis. The accumulation of ILC1s in skin and blood was specific to patients with sarcoidosis and not observed in other granulomatous diseases. The authors used a mouse model of lung granuloma to show that ILCs contribute to granuloma formation and that blockade of CXCR4 reduced the formation of granulomas, providing a proof of concept that sarcoidosis may be treated by CXCR4 blockade to prevent the progression of disease in patients. These results suggest ILC1s could serve as a diagnostic biomarker in sarcoidosis and a potential therapeutic target.
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页数:4
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