关键词: CD, cluster of differentiation DC, dendritic cell FoxP3, forkhead box IFN, interferon IFN-γ MLN, mesenteric lymph node NKT, natural killer T cell NOD mice PCA, principal component analysis PCoA, principal coordinate analysis PLN, pancreatic lymph node Treg, regulatory T cell Type 1 diabetes gut microbiota regulatory immunity siLP, small intestinal lamina propria

Mesh : Animals Bacteria / classification genetics Dendritic Cells / immunology Diabetes Mellitus, Type 1 / pathology Feces / microbiology Gastrointestinal Microbiome / immunology Gastrointestinal Tract / microbiology pathology Interferon-gamma / analysis Lymphocyte Subsets / immunology Mice, Inbred NOD

来  源:   DOI:10.1080/19490976.2015.1011876   PDF(Sci-hub)

Abstract:
Gut microbiota regulated imbalances in the host\'s immune profile seem to be an important factor in the etiology of type 1 diabetes (T1D), and identifying bacterial markers for T1D may therefore be useful in diagnosis and prevention of T1D. The aim of the present study was to investigate the link between the early gut microbiota and immune parameters of non-obese diabetic (NOD) mice in order to select alleged bacterial markers of T1D. Gut microbial composition in feces was analyzed with 454/FLX Titanium (Roche) pyro-sequencing and correlated with diabetes onset age and immune cell populations measured in diabetic and non-diabetic mice at 30 weeks of age. The early gut microbiota composition was found to be different between NOD mice that later in life were classified as diabetic or non-diabetic. Those differences were further associated with changes in FoxP3(+) regulatory T cells, CD11b(+) dendritic cells, and IFN-γ production. The model proposed in this work suggests that operational taxonomic units classified to S24-7, Prevotella, and an unknown Bacteriodales (all Bacteroidetes) act in favor of diabetes protection whereas members of Lachnospiraceae, Ruminococcus, and Oscillospira (all Firmicutes) promote pathogenesis.
摘要:
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