Effect of menstrual cycle variation in female sex hormones on cellular immunity and regulation

J Reprod Immunol. 2011 Apr;89(1):70-7. doi: 10.1016/j.jri.2010.11.009. Epub 2011 Mar 22.

Abstract

Ovarian steroid hormones reduce cell-mediated immunity (CMI), perhaps by increasing regulatory T cells. We examined the relationship of estrogen and progesterone plasma concentrations during the menstrual cycle with circulating regulatory T cells (Treg cells) and with varicella-zoster virus (VZV)-specific lymphocyte proliferation (VZV-LPA). Twenty healthy and 20 HIV-infected women were tested at 1-4, 10-14, and 20-24days of the menstrual cycle. HIV-infected women experienced significant increases in the frequency of peripheral blood CD4+IL10+ and CD8+FoxP3+ Treg cells from the early and late follicular phases to the luteal phase of their cycles. Healthy women experienced significant increases only in CD4+IL10+ Treg cells. The increase in CD4+IL10+ Treg cells between the late follicular and the luteal phases of HIV-infected and uninfected women significantly correlated with the corresponding increases in progesterone plasma concentrations. VZV-LPA results decreased from the early and late follicular phases to the luteal phase in both groups. The decrease in VZV-LPA results significantly correlated with the increase in CD4+IL10+ Treg cells underscoring the potential immunosuppressive effect of the progesterone-stimulated Treg cells. In conclusion, the increase in progesterone levels during the menstrual cycle was associated with higher Treg frequencies and lower CMI.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Adult
  • Antigens, Viral / immunology
  • CD4 Antigens / biosynthesis
  • CD8 Antigens / biosynthesis
  • Female
  • Forkhead Transcription Factors / biosynthesis
  • HIV / immunology*
  • HIV / pathogenicity
  • HIV Infections / immunology*
  • HIV Infections / physiopathology
  • Herpesvirus 3, Human / immunology*
  • Humans
  • Immunity, Cellular
  • Interleukin-10 / metabolism
  • Menstrual Cycle / blood
  • Menstrual Cycle / immunology
  • Middle Aged
  • Progesterone / blood
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism*
  • T-Lymphocyte Subsets / pathology
  • T-Lymphocyte Subsets / virology
  • T-Lymphocytes, Regulatory / immunology
  • T-Lymphocytes, Regulatory / metabolism*
  • T-Lymphocytes, Regulatory / pathology
  • T-Lymphocytes, Regulatory / virology

Substances

  • Antigens, Viral
  • CD4 Antigens
  • CD8 Antigens
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Interleukin-10
  • Progesterone