The Journal of Immunology · 2017 · 102 citations · 44 references
Life SciencesImmunologyMicrobiologyImmunoregulationInflammationInnate ImmunityGastrointestinal ImmunologyGastrointestinal InflammationMacrophage BiologyMucosal Immune SystemMucosal ImmunoregulationProbioticsBacillus SubtilisCd4 Positive T CellsCd8 Positive T CellsCd8 T Cell ActivationImmune Modulation By Gut MicrobesImmunomodulatory EffectsT-cell Immune ResponsesT-cell Mediated Responses
Abstract Commensal bacteria contribute to immune homeostasis in the gastrointestinal tract; however, the underlying mechanisms for this are not well understood. A single dose of exopolysaccharide (EPS) from the probiotic spore-forming bacterium Bacillus subtilis protects mice from acute colitis induced by the enteric pathogen Citrobacter rodentium. Adoptive transfer of macrophage-rich peritoneal cells from EPS-treated mice confers protection from disease to recipient mice. In vivo, EPS induces development of anti-inflammatory M2 macrophages in a TLR4-dependent manner, and these cells inhibit T cell activation in vitro and in C. rodentium–infected mice. In vitro, M2 macrophages inhibit CD4+ and CD8+ T cells. The inhibition of CD4+ T cells is dependent on TGF-β, whereas inhibition of CD8+ T cells is dependent on TGF-β and PD-L1. We suggest that administration of B. subtilis EPS can be used to broadly inhibit T cell activation and, thus, control T cell–mediated immune responses in numerous inflammatory diseases.
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