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在缺乏Vγ4和Vγ6 T细胞的情况下,Vγ1 T细胞对IL-17产生的部分补偿作用。

Partial Compensation of IL-17 Production by Vγ1 T Cells in the Absence of Vγ4 and Vγ6 T Cells.

作者信息

Wang Ziqing, Yang Tao, Lupo Federico, Behrens Lara-Marie, Janssen Anika, Coffelt Seth B, Prinz Immo, Sandrock Inga, Ravens Sarina

机构信息

Institute of Immunology, Hannover Medical School, Hannover, Germany.

School of Cancer Sciences, University of Glasgow, Glasgow, UK.

出版信息

Eur J Immunol. 2025 Sep;55(9):e70061. doi: 10.1002/eji.70061.

Abstract

γδ T cells are unconventional T cells that group into different subsets based on the usage of variable γδ T cell receptor (TCR) gene segments, body location, and functionality. γδ T cells that secrete the proinflammatory cytokine interleukin 17 (IL-17) predominantly express a Vγ4 or Vγ6 γδ TCR. The biology and the importance of the γδ TCR of IL-17-producing γδ T cells are not well understood. Here, we investigated the IL-17 production capability of γδ T cells in mice deficient for Vγ4 and Vγ6 γδ TCRs using flow cytometry, TCR-seq, and single-cell transcriptomics. Our data show that Vγ1 T cells only partially compensate for the loss of IL-17 Vγ4 and Vγ6 T cell subsets in lymphoid and nonlymphoid tissues. They develop pre- and postnatally and were predominantly detectable in their physiological body habitats. Collectively, the data underscore the nonredundant roles of Vγ4⁺ and Vγ6⁺ subsets in IL-17-mediated immunity.

摘要

γδ T细胞是非常规T细胞,根据可变γδ T细胞受体(TCR)基因片段的使用情况、身体位置和功能可分为不同亚群。分泌促炎细胞因子白细胞介素17(IL-17)的γδ T细胞主要表达Vγ4或Vγ6 γδ TCR。产生IL-17的γδ T细胞的γδ TCR的生物学特性及其重要性尚未完全了解。在此,我们使用流式细胞术、TCR测序和单细胞转录组学研究了缺乏Vγ4和Vγ6 γδ TCR的小鼠中γδ T细胞产生IL-17的能力。我们的数据表明,Vγ1 T细胞只能部分补偿淋巴组织和非淋巴组织中IL-17 Vγ4和Vγ6 T细胞亚群的缺失。它们在出生前和出生后发育,并且主要在其生理身体栖息地中被检测到。总体而言,这些数据强调了Vγ4⁺和Vγ6⁺亚群在IL-17介导的免疫中的非冗余作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e822/12449965/fa105992d80c/EJI-55-e70061-g002.jpg

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