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Innate lymphoid cells exhibited IL-17-expressing phenotype in active tuberculosis disease by Pan, Linyue (author);Chen, Xiaoli (author);Liu, Xuanqi (author);Qiu, Wenjia (author);Liu, Yunhuan (author);Jiang, Weiping (author);Zheng, Yang (author);Mou, Yan (author);Xu, Wei (author);Li, Xiangyang (author);Ge, Haiyan (author);Zhu, Huili (author) is a Medicine article available to read on EtoBox.

What is Innate lymphoid cells exhibited IL-17-expressing phenotype in active tuberculosis disease about?

## Background: Innate lymphoid cells (ilcs), as an important group of innate immunity, could respond rapidly to mycobacterium tuberculosis (mtb) infection. in this research, we studied the phenotypic changes of circulatory ilcs in active tuberculosis (tb) disease. ## Methods: We recruited 40 patients with active mtb infection (tb group) and 41 healthy subjects (nc group), and collected their clinical information and peripheral blood. circulating ilcs, ilc subsets, dendritic cells (dcs), macrophages, and the production of cytokines in ilcs were tested by flow cytometry (fcm). enzyme-linked immunosorbent assay (elisa) was used to detect plasma il-23. ## Results: Compared with healthy control, total ilcs (0.73% vs. 0.42%, p = 0.0019), ilc1 (0.55% vs. 0.31%, p = 0.0024) and cd117 ilc2 (0.02% vs. 0.01%, p = 0.0267) were upregulated in tb group. the total il-17 lymphocytes were elevated (3.83% vs. 1.76%, p = 0.0006) while the il-22 lymphocytes remained unchanged. within ilc subsets, ilc3, cd117 ilc2 and ilc1 in tb group all expressed increased il-17 (15.15% vs. 4.55%, 19.01% vs. 4.57%, 8.79% vs. 3.87%, p < 0.0001) but similar il-22 comparing with healthy control. tb group had more plasma

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Author
Pan, Linyue (author);Chen, Xiaoli (author);Liu, Xuanqi (author);Qiu, Wenjia (author);Liu, Yunhuan (author);Jiang, Weiping (author);Zheng, Yang (author);Mou, Yan (author);Xu, Wei (author);Li, Xiangyang (author);Ge, Haiyan (author);Zhu, Huili (author)
Publisher
Springer Science and Business Media LLC
Published
2021
Language
EN
Field
Medicine (Health Sciences)

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