Cited by 320T-cell and B-cell ImmunologyGut microbiota and healthImmunotherapy and Immune Responses

Microbial metabolites control the thymic development of mucosal-associated invariant T cells

Legoux, François, Bellet, Déborah, Daviaud, Celine, El Morr, Yara, Darbois, Aurelie, Niort, Kristina, Procopio, Emanuele, Salou, Marion +9 more·2019·Science

Abstract

Commensals rule the MAITrix: Mucosal-associated invariant T (MAIT) cells play an important role in mucosal homeostasis. MAIT cells recognize microbial small molecules presented by the major histocompatibility complex class Ib molecule MR1. MAIT cells are absent in germ-free mice, and the mechanisms by which microbiota control MAIT cell development are unknown (see the Perspective by Oh and Unutmaz). Legoux et al. show that, in mice, development of MAIT cells within the thymus is governed by the bacterial product 5-(2-oxopropylideneamino)-6- d -ribitylaminouracil, which rapidly traffics from the mucosa to the thymus, where it is captured by MR1 and presented to developing MAIT cells. Constantinides et al. report that MAIT cell induction only occurs during a limited, early-life window and requires exposure to defined microbes that produce riboflavin derivatives. Continual interactions between MAIT cells and commensals in the skin modulates tissue repair functions. Together, these papers highlight how the microbiota can direct immune cell development and subsequent function at mucosal sites by secreting compounds that act like self-antigens. Science , this issue p. 494 , p. eaax6624 ; see also p. 419

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Crossref · 10.1126/science.aaw2719

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  • The development and maturation of MAIT cells are dependent on microbiota, as demonstrated by reduced numbers of MAIT cells in GF mice, which can be restored through microbial colonization.

    “The development and maturation of MAIT cells are dependent on microbiota, as demonstrated by reduced numbers of MAIT cells in GF mice, which can be restored through microbial colonization.”

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References 34 · Cited by 320

Authors
Legoux, F., Bellet, D., Daviaud, C., El Morr, Y., Darbois, A., Niort, K., Procopio, E., Salou, M., Gilet, J., Ryffel, B., Balvay, A., Foussier, A., Sarkis, M., El Marjou, A., Schmidt, F., Rabot, S., & Lantz, O.
Affiliations
  • INSERM U932, PSL University, Institut Curie, Paris 75005, France.
  • AgroParisTech (FR)
  • Institut Curie (FR)
  • Inserm (FR)
  • Université d'Orléans (FR)
  • Centre National de la Recherche Scientifique (FR)
  • Recombinant Protein Facility, Institut Curie, Paris 75005, France.
  • CNRS UMR3666, INSERM U1143, PSL University, Institut Curie, Paris 75005, France.
Corresponding author
Lantz, Olivier
Venue
Science
Published
2019-10-25
Volume
366
Issue
6464
Pages
494-499
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2970705750
Cited by
320
References
34
Citations by year
2026: 26 · 2025: 34 · 2024: 40 · 2023: 42 · 2022: 57 · 2021: 43 · 2020: 64 · 2019: 13
FWCI
18.15
Type
journal article
Language
en
Open access
closed
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
Funders
Agence Nationale de la Recherche (MAIT, NEOMAIT, DIABMAIT, DCBIOL)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
Keywords
mucosal-associated invariant T cells, thymus development, gut microbiota, MR1, microbial metabolites, riboflavin derivatives, commensal bacteria, mucosal immunity, tissue repair, germ-free mice
MeSH terms
Gastrointestinal Microbiome, Mucosal-Associated Invariant T Cells, Animals, Escherichia coli, Germ-Free Life, Lung, Mice, Inbred C57BL, Mucous Membrane, Nucleotide Deaminases, Receptors, Antigen, T-Cell, Ribitol, Specific Pathogen-Free Organisms, Spleen, Sugar Alcohol Dehydrogenases, Symbiosis, Thymus Gland, Uracil, Histocompatibility Antigens Class I, Minor Histocompatibility Antigens, Mice, Knockout, Escherichia coli Proteins, Mice

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