Distinct peripheral vs mucosal T-cell phenotypes in chlamydia-infected women

Am J Reprod Immunol. 2017 Dec;78(6):10.1111/aji.12768. doi: 10.1111/aji.12768. Epub 2017 Sep 26.

Abstract

Problem: Differences in circulating (peripheral) and mucosal T-cell phenotypes in chlamydia-infected women remain largely unknown.

Method of study: Thirteen paired mononuclear cell specimens from blood and cervicovaginal lavages collected from chlamydia-infected women were stained and analyzed using ten-color cell surface flow cytometry for T-cell distribution, activation status, homing, and T helper (Th)-associated chemokine receptors (CKRs).

Results: A higher proportion of genital mucosal T-cells were activated (CD38+ HLA-DR+ ) and expressed CCR5 and Th1-associated CKR CXCR3+ CCR5+ compared to peripheral T-cells, but a lower proportion of mucosal T-cells expressed homing CKR CCR7, Th-2 associated CKR CCR4, and CXCR3+ CCR4+ for both T-cell subsets.

Conclusion: T-cell phenotypes differed in the peripheral vs genital mucosa compartments in chlamydia-infected women. As chlamydia infects mucosal epithelial cells, the finding of a higher frequency of activated T-cells and Th-1 phenotypes in the mucosa likely reflects an adaptive immune response to infection.

Keywords: Chlamydia; T-cell; mucosal; peripheral; phenotype; receptor.

Publication types

  • Comparative Study

MeSH terms

  • Adaptive Immunity
  • Adult
  • Animals
  • Blood Cells / immunology*
  • Cell Separation
  • Chlamydia / immunology*
  • Chlamydia Infections / immunology*
  • Female
  • Flow Cytometry
  • Humans
  • Immunophenotyping
  • Lymphocyte Activation
  • Mice
  • Mucous Membrane / pathology*
  • Phenotype
  • T-Lymphocyte Subsets / immunology
  • Th1 Cells / immunology*
  • Vagina / pathology*