Dysregulation of the vitamin D nuclear receptor may contribute to the higher prevalence of some autoimmune diseases in women

Ann N Y Acad Sci. 2009 Sep;1173:252-9. doi: 10.1111/j.1749-6632.2009.04672.x.

Abstract

Researchers have noted that the incidence of autoimmune diseases, such as Hashimoto's thyroiditis, is markedly higher in women than in men, but to date the reason for this disparity has been unclear. The vitamin D nuclear receptor (VDR) is expressed in the human cycling endometrium. Because the VDR controls expression of the cathelicidin and beta-defensin antimicrobial peptides (AmPs), dysregulation of the receptor greatly compromises the innate immune response. Increasing evidence indicates the presence of a chronic, intraphagocytic, metagenomic microbiota in patients with autoimmune disease that may survive by dysregulating the VDR. VDR dysregulation, in turn, prevents the breakdown of the active vitamin D metabolite 1,25-hydroxyvitamin D (1,25-D) by CYP24. In silico data suggest that when 1,25-D rises above its normal range, it binds the alpha/beta thyroid receptors, the glucocorticoid receptor (GCR), and the androgen receptor (AR), displacing their native ligands and causing an array of hormonal imbalances. If T3 is displaced from alpha-thyroid, thyroiditis may result. Because the VDR, GCR, and AR also express multiple families of AmPs, expression of these natural antibiotics further wanes in response to dysregulation by 1,25-D. The end result is a system-wide drop in AmP expression that may allow pathogens to spread with greater ease. Because women have an extra site of VDR expression in the endometrium, the drop in AmP expression associated with nuclear receptor dysregulation may disproportionately affect them. This would cause women to accumulate higher bacterial loads than their male counterparts, particularly during early pregnancy when 1,25-D levels rise by 40%.

MeSH terms

  • Antimicrobial Cationic Peptides / metabolism
  • Autoimmune Diseases / metabolism
  • Autoimmune Diseases / physiopathology*
  • Binding Sites
  • Calcitriol / metabolism
  • Cell Nucleus / metabolism*
  • Endometrium / metabolism
  • Female
  • Humans
  • Immunity, Innate / physiology
  • Ligands
  • Male
  • Pregnancy
  • Receptors, Calcitriol / metabolism
  • Receptors, Calcitriol / physiology*
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Receptors, Cytoplasmic and Nuclear / physiology
  • Sex Factors
  • Steroid Hydroxylases / metabolism
  • Vitamin D3 24-Hydroxylase
  • beta-Defensins / metabolism

Substances

  • Antimicrobial Cationic Peptides
  • Ligands
  • Receptors, Calcitriol
  • Receptors, Cytoplasmic and Nuclear
  • beta-Defensins
  • CAP18 lipopolysaccharide-binding protein
  • Steroid Hydroxylases
  • Vitamin D3 24-Hydroxylase
  • Calcitriol