Gut microbiota promotes immune tolerance at the maternal-fetal interface.

TitleGut microbiota promotes immune tolerance at the maternal-fetal interface.
Publication TypeJournal Article
Year of Publication2026
AuthorsBrown JA, Amir M, Yu S, Wong DSH, Gu J, Balaji U, Parkhurst CN, Hong S, Hart LR, Carrow HC, Bah MA, Ananthanarayanan A, Sanidad KZ, Lyu M, Siddikova A, Santos MLima Silva, Serganova I, Diehl GE, Anrather J, Inohara N, Sonnenberg GF, Pascual V, Zeng MY
JournalCell
Volume189
Issue1
Pagination196-214.e24
Date Published2026 Jan 08
ISSN1097-4172
KeywordsAbortion, Habitual, Animals, Female, Gastrointestinal Microbiome, Humans, Immune Tolerance, Interferon-gamma, Interleukin-17, Maternal-Fetal Exchange, Mice, Mice, Inbred C57BL, Myeloid-Derived Suppressor Cells, Nuclear Receptor Subfamily 1, Group F, Member 3, Placenta, Pregnancy, T-Lymphocytes, Regulatory, Tryptophan
Abstract

Immune tolerance at the maternal-fetal interface (MFI) is required for fetal development. Excessive maternal interferon-gamma (IFN-γ) and interleukin-17 (IL-17) are linked to pregnancy complications, but the regulation of maternal IFN-γ and IL-17 at the MFI is poorly understood. Here, we demonstrate a gut-placenta immune axis in pregnant mice in which the absence or perturbation of gut microbiota dysregulates maternal IFN-γ and IL-17 responses at the MFI, resulting in fetal resorption. Microbiota-dependent tryptophan derivatives suppress IFN-γ+ and IL-17+ T cells at the MFI by priming myeloid-derived suppressor cells (MDSCs) and gut-derived RORγt+ regulatory T cells (Tregs), respectively. The tryptophan derivative indole-3-carbinol, or tryptophan-metabolizing Lactobacillus murinus, rebalances the T cell response at the MFI and reduces fetal resorption in germ-free mice. Furthermore, MDSCs, RORγt+ Tregs, and microbiota-dependent tryptophan derivatives are dysregulated at the MFI in human recurrent miscarriage cases. Together, our findings identify microbiota-dependent immune tolerance mechanisms that promote fetal development.

DOI10.1016/j.cell.2025.11.022
Alternate JournalCell
PubMed ID41412123