Reduced frequency of perforin-positive CD8+ T cells in menstrual effluent of endometriosis patients compared to healthy controls

Author:

Schmitz Timo,Hoffmann Verena,Olliges Elisabeth,Bobinger Alina,Popovici Roxana,Nößner Elfriede,Meissner Karin

Abstract

AbstractBackgroundEndometriosis is widespread among women in reproductive age and quite commonly reduces life quality of those affected by symptoms like dysmenorrhea, dyspareunia or infertility. The scientific literature indicates many immunological changes like reduced cytotoxicity of natural killer cells or altered concentrations of cytokines and cell adhesion molecules. Frequently examined tissues are peripheral blood, endometrial tissue and peritoneal fluid. Yet, knowledge on immunological differences in menstrual effluent (ME) is scarce.Methods12 women with endometriosis and 11 healthy controls were included in this study. ME was collected using menstrual cups and venous blood samples (PB) were taken. Mononuclear cells were obtained from ME (MMC) and PB (PBMC) and analyzed using flow cytometry. Furthermore, concentrations of cell adhesion molecules (ICAM-I and VCAM-I) and cytokines (IL-6, IL-8 and TNF-α) were measured in ME and PB.ResultsCD8+ T cells obtained from ME were significantly less often perforin-positive in women with endometriosis compared to healthy controls. Additionally, plasma ICAM-I concentrations were significantly lower in the endometriosis group. A comparison between MMC and PBMC revealed that MMC contained significantly less T cells and more B cells. The CD4/CD8 ratio was significantly higher in MMC, and Tregs were significantly less frequently in MMC. In ME, T cells and NK cells expressed significantly more CD69. NK cells obtained from ME were predominantly CD56bright/CD16dim and had a lower frequency of perforin+ cells compared to PBMC NK cells. NKp46 was significantly more expressed on NK cells from PBMC.ConclusionCD8+ T cells obtained from the ME were significantly less perforin-positive in endometriosis patients indicating a reduced cytotoxic potential. MMC are distinctively different from PBMC and, thus, seem to be of endometrial origin.

Publisher

Cold Spring Harbor Laboratory

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