Peritoneal natural killer cell chemotaxis is decreased in women with pelvic endometriosis
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Peritoneal NK cell chemotaxis was significantly lower in women with endometriosis compared to controls, and this decrease persisted throughout the menstrual cycle.
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Abstract
PROBLEM: NK cell and macrophage function are decreased in endometriosis, and the disease may involve reduced immune surveillance in the peritoneal cavity. NK cell cytotoxicity and migration ability (chemotaxis) are considered important; the former has been investigated, but the latter has not. METHOD OF STUDY: We compared chemotaxis of immunocompetent cells (NK cells, macrophages, T cells) in peritoneal fluid obtained during laparoscopy in 27 women with and 13 without endometriosis. Peripheral blood NK cells were also obtained by the peripheral blood antibody beads method. Micro-cultured cells were examined by time-lapse photography, and the mean migration speed per cell was calculated as the chemotaxis. We investigated the relationship between chemotaxis and endometriosis. RESULTS: NK cell chemotaxis was significantly lower in the endometriosis group. Macrophages and lymphocytes were not significantly different between the groups. During menstruation, NK cell chemotaxis decreased in both groups. Postmenstrual chemotaxis was increased significantly in women without endometriosis but remained low in women with endometriosis. The Revised-American Society for Reproductive Medicine score was not correlated with chemotaxis; in women with endometriosis, chemotaxis was decreased even at early stages. Peripheral blood NK cells showed no significant differences. CONCLUSIONS: In women with endometriosis, not only cytotoxicity but also chemotaxis by NK cells in peritoneal cavity is significantly decreased, and particularly chemotaxis is decreased throughout the menstrual cycle. Therefore, antigens in retrograde menstrual blood that enters the peritoneal cavity might be left unprocessed. Repetition of this immune process in the peritoneal cavity may lead to the onset and subsequent progression of endometriosis.
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Cited by (11)
- Identification and Validation of Potential Immune‐Related Genes for Endometriosis 2025
- Immunological aspects of endometriosis: pathophysiological mechanisms, diagnosis, autoimmunity, targeted therapy and modulation 2024
- Proangiogenic properties of complement protein C1q can contribute to endometriosis 2024
- An Estrogen–NK Cells Regulatory Axis in Endometriosis, Related Infertility, and Miscarriage 2024
- Additional file 2 of Signatures of necroptosis-related genes as diagnostic markers of endometriosis and their correlation with immune infiltration 2024
- Additional file 2 of Signatures of necroptosis-related genes as diagnostic markers of endometriosis and their correlation with immune infiltration 2024
- The Role of Peritoneal Immunity in Peritoneal Endometriosis and Related Infertility 2023
- Signatures of necroptosis-related genes as diagnostic markers of endometriosis and their correlation with immune infiltration 2023
- Signatures of necroptosis-related genes as diagnostic markers of endometriosis and their correlation with immune infiltration 2023
- Validation of Contour Extraction Using YOLACT for Analysis of NK Cell Chemotaxis 2023
- Non-invasive diagnosis of endometriosis: Immunologic and genetic markers 2022
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