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Human gut bacterial metabolism drives Th17 activation and colitis

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High-resolution mycobiota analysis reveals dynamic intestinal translocation preceding invasive candidiasis

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Oral epithelial IL-22/STAT3 signaling licenses IL-17–mediated immunity to oral mucosal candidiasis

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Ribosome-Targeting Antibiotics Impair T Cell Effector Function and Ameliorate Autoimmunity by Blocking Mitochondrial Protein Synthesis

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Microbiota Sensing by Mincle-Syk Axis in Dendritic Cells Regulates Interleukin-17 and -22 Production and Promotes Intestinal Barrier Integrity

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Commensal Candida albicans Positively Calibrates Systemic Th17 Immunological Responses

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The Bone Marrow Protects and Optimizes Immunological Memory during Dietary Restriction

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A dysbiotic microbiome triggers TH17 cells to mediate oral mucosal immunopathology in mice and humans

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Antibiotic Treatment Affects Intestinal Permeability and Gut Microbial Composition in Wistar Rats Dependent on Antibiotic Class

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Microbiota-Dependent Crosstalk Between Macrophages and ILC3 Promotes Intestinal Homeostasis

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Bactericidal Antibiotics Induce Mitochondrial Dysfunction and Oxidative Damage in Mammalian Cells

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Interactions Between Commensal Fungi and the C-Type Lectin Receptor Dectin-1 Influence Colitis

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Specific Microbiota Direct the Differentiation of IL-17-Producing T-Helper Cells in the Mucosa of the Small Intestine

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Vancomycin-resistant enterococci exploit antibiotic-induced innate immune deficits

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Mucosal Damage and Neutropenia Are Required for Candida albicans Dissemination

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