4.8 Article

Gender Bias in Autoimmunity Is Influenced by Microbiota

Journal

IMMUNITY
Volume 39, Issue 2, Pages 400-412

Publisher

CELL PRESS
DOI: 10.1016/j.immuni.2013.08.013

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Funding

  1. National Institutes of Health [AI082418]
  2. Juvenile Diabetes Research Foundation [17-2011-519]
  3. NIH/NIDDK Digestive Disease Research Core Center [DK42086]
  4. Molecular and Cellular Biology training grant [T32 GM007183]
  5. Clinical Translational Science Award TL1 training grant [TL1TR000432]
  6. NIH [p50 GM081892]
  7. Searle Funds at the Chicago Community Trust

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Gender bias and the role of sex hormones in autoimmune diseases are well established. In specific pathogen-free nonobese diabetic (NOD) mice, females have 1.3-4.4 times higher incidence of type 1 diabetes (T1D). Germ-free (GF) mice lost the gender bias (female-to-male ratio 1.1-1.2). Gut microbiota differed in males and females, a trend reversed by male castration, confirming that androgens influence gut microbiota. Colonization of GF NOD mice with defined microbiota revealed that some, but not all, lineages overrepresented in male mice supported a gender bias in T1D. Although protection of males did not correlate with blood androgen concentration, hormone-supported expansion of selected microbial lineages may work as a positive-feedback mechanism contributing to the sexual dimorphism of autoimmune diseases. Gene-expression analysis suggested pathways involved in protection of males from T1D by microbiota. Our results favor a two-signal model of gender bias, in which hormones and microbes together trigger protective pathways.

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