Zeng Qunxiong, Liu Jin-Chuan, Yang Chen, Lyu Minmin, Li Dongliang, Yeung William S B, Chiu Philip C N, Zhang Tao, Duan Yong-Gang
Shenzhen Key Laboratory of Fertility Regulation, Center of Assisted Reproduction and Embryology, the University of Hong Kong - Shenzhen Hospital, Shenzhen 518053, China.
Department of Obstetrics and Gynaecology, the University of Hong Kong, Pokfulam Road, Hong Kong, China.
iScience. 2025 Apr 23;28(5):112508. doi: 10.1016/j.isci.2025.112508. eCollection 2025 May 16.
Inflammatory bowel disease (IBD) is linked to male fertility disorders, yet the role of gut microbiota dysbiosis remains underexplored. Here, we investigated how dysbiosis contributes to autoimmune epididymo-orchitis in a colitis mouse model induced by CD4 T cell transfer. We transferred wild-type CD4 T cells into male mice, with some groups pretreated with antibiotics or receiving or CD4 T cells. Through gut microbiota profiling, histopathology evaluation, immune cell infiltration assessments in the reproductive tissues, and sperm analysis, we observed severe gut dysbiosis, colon inflammation, and reproductive impairments characterized by leukocyte infiltration in mice transferred with wild-type T cells. Interestingly, these impairments were mitigated in groups pretreated with antibiotics or receiving cells but not CD4 T cells. These findings highlight that gut microbiota dysbiosis can initiate Th17 cell-mediated reproductive disorders, offering insights for potential therapeutic interventions in IBD-related male infertility.
炎症性肠病(IBD)与男性生育障碍有关,但肠道微生物群失调的作用仍未得到充分研究。在此,我们在由CD4 T细胞转移诱导的结肠炎小鼠模型中研究了失调如何导致自身免疫性附睾睾丸炎。我们将野生型CD4 T细胞转移到雄性小鼠体内,一些组用抗生素预处理或接受 或 CD4 T细胞。通过肠道微生物群分析、组织病理学评估、生殖组织中的免疫细胞浸润评估和精子分析,我们观察到在转移了野生型T细胞的小鼠中存在严重的肠道失调、结肠炎症和以白细胞浸润为特征的生殖损伤。有趣的是,在用抗生素预处理或接受 细胞的组中,这些损伤得到缓解,但接受 CD4 T细胞的组没有。这些发现突出表明肠道微生物群失调可引发Th17细胞介导的生殖障碍,为IBD相关男性不育的潜在治疗干预提供了见解。