4.7 Article

Characterization of the Genital Mucosa Immune Profile to Distinguish Phases of the Menstrual Cycle: Implications for HIV Susceptibility

Journal

JOURNAL OF INFECTIOUS DISEASES
Volume 219, Issue 6, Pages 856-866

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiy585

Keywords

Genital inflammation; HIV; menstrual cycle; immune activation

Funding

  1. Canadian Institutes of Health Research (CIHR) [MOP 86721]
  2. Fond de la recherche-Sante
  3. CIHR International Infectious Diseases and Global Health Training Program

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Here, we compared the impact of endogenous sexual hormones on the mucosal immune response. Our study shows that the follicular phase of the menstrual cycle was associated with elevated level of cervical CCL2 and retention of resident memory CD4(+) T cells.Inflammation and immune activation are key factors in sexual transmission of human immunodeficiency virus (HIV). We sought to define the impact of hormonal cycling on the mucosal immune environment and HIV risk in sex workers with a natural menstrual cycle. We compared soluble mucosal immune factors and cervical mononuclear cells during hormone titerdefined phases of the menstrual cycle among 37 sex workers from Nairobi, Kenya. Systemic and mucosal samples were collected 14 days apart to distinguish the follicular and luteal phases of the menstrual cycle, and phases were confirmed by hormone measurements. Vaginal concentrations of 19 immune modulators and cervical T-cell activation markers were measured. The follicular phase signature was characterized by an elevated CCL2 level, decreased interleukin 1 and interleukin 1 cervical concentrations, and a significant increase in the proportion of CD4(+) T cells that expressed CD69. The genital concentration of CCL2 was the best marker to distinguish the follicular from the luteal phase in univariate and multivariate analyses and remained independent of elevated genital inflammation and bacterial vaginosis. The follicular phase of the menstrual cycle was associated with an elevated CCL2 level and retention of resident memory CD4(+) T cells, which has implications for increased susceptibility to HIV infection.

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