Obesity intensifies sex-specific interferon signaling to selectively worsen central nervous system autoimmunity in females

Cell Metab. 2024 Oct 1;36(10):2298-2314.e11. doi: 10.1016/j.cmet.2024.07.017. Epub 2024 Aug 20.

Abstract

Obesity has been implicated in the rise of autoimmunity in women. We report that obesity induces a serum protein signature that is associated with T helper 1 (Th1), interleukin (IL)-17, and multiple sclerosis (MS) signaling pathways selectively in human females. Females, but not male mice, subjected to diet-induced overweightness/obesity (DIO) exhibited upregulated Th1/IL-17 inflammation in the central nervous system during experimental autoimmune encephalomyelitis, a model of MS. This was associated with worsened disability and a heightened expansion of myelin-specific Th1 cells in the peripheral lymphoid organs. Moreover, at steady state, DIO increased serum levels of interferon (IFN)-α and potentiated STAT1 expression and IFN-γ production by naive CD4+ T cells uniquely in female mice. This T cell phenotype was driven by increased adiposity and was prevented by the removal of ovaries or knockdown of the type I IFN receptor in T cells. Our findings offer a mechanistic explanation of how obesity enhances autoimmunity.

Keywords: T cells; T helper 1 differentiation; autoimmunity; experimental autoimmune encephalomyelitis; interferon-α; multiple sclerosis; obesity; sex differences.

MeSH terms

  • Animals
  • Autoimmunity*
  • Central Nervous System* / immunology
  • Central Nervous System* / metabolism
  • Encephalomyelitis, Autoimmune, Experimental* / immunology
  • Encephalomyelitis, Autoimmune, Experimental* / metabolism
  • Encephalomyelitis, Autoimmune, Experimental* / pathology
  • Female
  • Humans
  • Interleukin-17 / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL*
  • Multiple Sclerosis / immunology
  • Multiple Sclerosis / metabolism
  • Obesity* / immunology
  • Obesity* / metabolism
  • STAT1 Transcription Factor / metabolism
  • Sex Characteristics
  • Sex Factors
  • Signal Transduction*
  • Th1 Cells / immunology
  • Th1 Cells / metabolism

Substances

  • STAT1 Transcription Factor
  • Interleukin-17