γδ T cells compose a developmentally regulated intrauterine population and protect against vaginal candidiasis

γδ T 细胞构成发育调控的子宫内细胞群,并能抵抗阴道念珠菌病。

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作者:L Monin ,D S Ushakov ,H Arnesen ,N Bah ,A Jandke ,M Muñoz-Ruiz ,J Carvalho ,S Joseph ,B C Almeida ,M J Green ,E Nye ,S Hatano ,Y Yoshikai ,M Curtis ,H Carlsen ,U Steinhoff ,P Boysen ,A Hayday

Abstract

This most comprehensive analysis to date of γδ T cells in the murine uterus reveals them to compose a unique local T-cell compartment. Consistent with earlier reports, most cells expressed a canonical Vγ6Vδ1 TCR, and produced interleukin (IL)-17A upon stimulation. Nonetheless, contrasting with earlier reports, uterine γδ T cells were not obviously intraepithelial, being more akin to sub-epithelial Vγ6Vδ1+ T cells at several other anatomical sites. By contrast to other tissues however, the uterine compartment also included non-Vγ6+, IFN-γ-producing cells; was strikingly enriched in young mice; expressed genes hitherto associated with the uterus, including the progesterone receptor; and did not require microbes for development and/or maintenance. This notwithstanding, γδ T-cell deficiency severely impaired resistance to reproductive tract infection by Candida albicans, associated with decreased responses of IL-17-dependent neutrophils. These findings emphasise tissue-specific complexities of different mucosal γδ cell compartments, and their evident importance in lymphoid stress-surveillance against barrier infection.

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