4.6 Article

The Role of Selected Chemokines in the Peritoneal Fluid of Women with Endometriosis-Participation in the Pathogenesis of the Disease

Journal

PROCESSES
Volume 9, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/pr9122229

Keywords

endometriosis; chemokines; peritoneal fluid; inflammation

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Endometriosis is characterized by the presence of endometrial tissue outside the uterus, and associated with immune dysregulation. The study aimed to investigate the role of chemokines in endometriosis development, finding that certain chemokines in peritoneal fluid may play a key role in disease pathogenesis, with concentrations correlating with disease severity.
Endometriosis is a disorder characterized by the presence of endometrial tissue outside the uterine cavity, primarily into the peritoneal cavity. It is known as a complex, chronic inflammatory disease and it is strongly associated with immune dysregulation. Various soluble mediators of the immune and inflammatory responses, including chemokines, play an important role in these processes. The aim of the study was to understand the role of the chemokines MCP-1, MCP-2, MCP-3, MCP-4, MIP-1 alpha, MIP-1 beta, eotaxin 2, eotaxin 3, ENA-78, and fractalkine in the development of endometriosis through their assessment in the peritoneal fluid of women with endometriosis. The study group included 58 women with endometriosis who were diagnosed during laparoscopy and then confirmed by histopathology. In 15 women from the reference group, laparoscopic examination demonstrated a normal status of the pelvic organs without any evidence of endometriosis nor inflammation in the peritoneal cavity. The peritoneal fluid of women with endometriosis and of women from the reference group were examined. To determine the concentration of the studied chemokines, enzyme immunoassays for Luminex(R) platforms were used. In the peritoneal fluid of women with endometriosis, a statistically significant increase in the concentration of MIP-1 beta, eotaxin 2, eotaxin 3, ENA-78, and fractalkine and a decrease in the concentration of MCP-1, MCP-2, MCP-3, MCP-4, and MIP-1 alpha were observed compared to the reference group. The concentration of these cytokines depended on the severity of the disease. Changes in the concentration of the studied chemokines in the peritoneal fluid of women with endometriosis suggest their participation in the pathogenesis of the disease. The differences in chemokines concentration observed in different stages of endometriosis may be associated with the presence of inflammation in the peritoneal cavity at each step of disease development.

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