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Article: Gut microbiota-driven pathogenic Th17 cells mediated autoimmune epididymo-orchitis in a mouse model of colitis

TitleGut microbiota-driven pathogenic Th17 cells mediated autoimmune epididymo-orchitis in a mouse model of colitis
Authors
KeywordsBiological sciences
Immune response
Immune system
Immunology
Microbiology
Issue Date16-May-2025
PublisherCell Press
Citation
iScience, 2025, v. 28, n. 5 How to Cite?
AbstractInflammatory 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 Rag1−/− mice, with some groups pretreated with antibiotics or receiving Il-17a−/− or Ccr6−/− 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 Il-17a−/− cells but not Ccr6−/− 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.
Persistent Identifierhttp://hdl.handle.net/10722/358124
ISSN
2023 Impact Factor: 4.6
2023 SCImago Journal Rankings: 1.497
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZeng, Qunxiong-
dc.contributor.authorLiu, Jin Chuan-
dc.contributor.authorYang, Chen-
dc.contributor.authorLyu, Minmin-
dc.contributor.authorLi, Dongliang-
dc.contributor.authorYeung, William S.B.-
dc.contributor.authorChiu, Philip C.N.-
dc.contributor.authorZhang, Tao-
dc.contributor.authorDuan, Yong Gang-
dc.date.accessioned2025-07-24T00:30:36Z-
dc.date.available2025-07-24T00:30:36Z-
dc.date.issued2025-05-16-
dc.identifier.citationiScience, 2025, v. 28, n. 5-
dc.identifier.issn2589-0042-
dc.identifier.urihttp://hdl.handle.net/10722/358124-
dc.description.abstractInflammatory 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<sup>+</sup> T cell transfer. We transferred wild-type CD4<sup>+</sup> T cells into male Rag1<sup>−/−</sup> mice, with some groups pretreated with antibiotics or receiving Il-17a<sup>−/−</sup> or Ccr6<sup>−/−</sup> CD4<sup>+</sup> 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 Il-17a<sup>−/−</sup> cells but not Ccr6<sup>−/−</sup> CD4<sup>+</sup> 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.-
dc.languageeng-
dc.publisherCell Press-
dc.relation.ispartofiScience-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectBiological sciences-
dc.subjectImmune response-
dc.subjectImmune system-
dc.subjectImmunology-
dc.subjectMicrobiology-
dc.titleGut microbiota-driven pathogenic Th17 cells mediated autoimmune epididymo-orchitis in a mouse model of colitis -
dc.typeArticle-
dc.identifier.doi10.1016/j.isci.2025.112508-
dc.identifier.scopuseid_2-s2.0-105004378477-
dc.identifier.volume28-
dc.identifier.issue5-
dc.identifier.eissn2589-0042-
dc.identifier.isiWOS:001509714300001-
dc.identifier.issnl2589-0042-

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