Association between FOXP3+ regulatory T-cells and occurrence of peritoneal lesions in women with ovarian endometrioma and dermoid cysts
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This study investigated the relationship between FOXP3+ regulatory T-cells and the presence of peritoneal lesions in women diagnosed with ovarian endometrioma and dermoid cysts.
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Abstract
Research questionIs there any relationship between numbers of FOXP3+ regulatory T-cells (Treg) and occurrence of peritoneal lesions in women with ovarian endometrioma and dermoid cysts?DesignRetrospective and prospective case-controlled cohort study. Peritoneal lesions were collected from 27 women with ovarian endometrioma and 25 women with dermoid cysts. Peritoneal fluid was collected from 36 women with ovarian endometrioma and 42 women with dermoid cysts. Tissue expression of Forkhead box P3 (FOXP3), one of the transcription factors of Treg cells, and transforming growth factor-beta (TGF-β) were examined by immunohistochemistry. Interleukin-6 (IL-6) and TGF-β levels in the peritoneal fluid were measured by enzyme-linked immunosorbent assay.ResultsOvarian endometrioma cases with coexisting peritoneal lesions were significantly more frequent than dermoid cyst cases with coexistent peritoneal lesions (269/350 [76.9%] versus 74/414 [17.9%]; P < 0.001). Numbers of FOXP3+ Treg cells were significantly higher in peritoneal lesions of women coexistent with ovarian endometrioma (F = 21.52, P < 0.001) and dermoid cysts (F = 22.01, P < 0.001) compared with women without peritoneal lesions. Higher FOXP3+ Treg cell numbers in pathological lesions corresponded with significantly higher TGF-β (P < 0.001) and lower IL-6 (P = 0.020) levels in peritoneal fluid of women with peritoneal lesions compared with women without lesions.ConclusionsThis study confirms current speculation that endometriosis is related to alteration in Treg cells, causing survival and implantation of ectopic endometrial lesions in women with endometrioma and dermoid cysts. The findings may clarify why only 10% of women in the general population develop endometriosis despite cyclic menstruation with retrograde flow occurring in >90% of women.
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Cited by (18)
- Immune mechanisms in the pathogenesis of endometriosis: a comprehensive analysis of the role of NK cells, cytokines, and extracellular vesicles/exosomes 2026
- PBMC-derived FGF, PDGF, VEGF and GM-CSF secretion in endometriosis: a case-control in vitro study 2026
- Oxidative Stress and Antioxidant Capacity in Patients with Endometrioma 2024
- Research Progress of FOXP3 and TGF-β1 in Diagnosis and Treatment of Endometriosis 2024
- Unraveling the microbial puzzle: exploring the intricate role of gut microbiota in endometriosis pathogenesis 2024
- The role of regulatory T-cells in the development of endometriosis 2024
- The role of innate and adaptive immunity in endometriosis 2024
- Immune and endocrine regulation in endometriosis: what we know 2023
- Peritoneal immune microenvironment of endometriosis: Role and therapeutic perspectives 2023
- ATG8 inhibited endometriosis formation by regulating Treg cells differentiation via integrin α4β1 and Talin-1 interaction 2023
- Interleukin-33 Derived from Endometriotic Lesions Promotes Fibrogenesis through Inducing the Production of Profibrotic Cytokines by Regulatory T Cells 2022
- Laparoscopic removal of a dermoid cyst in one ovary and an endometrioma in the other: A case report and literature review 2022
- Role of Th1, Th2, Th17, and regulatory T cells in endometriosis 2021
- The role of dendritic cells in endometriosis: A systematic review 2021
- Inflammation related to high-mobility group box-1 in endometrial ovarian cyst 2021
- Pathophysiological Basis of Endometriosis-Linked Stress Associated with Pain and Infertility: A Conceptual Review 2020
- Alteration of systemic and uterine endometrial immune populations in patients with endometriosis 2020
- Differential Levels of Regulatory T Cells and T-Helper-17 Cells in Women With Early and Advanced Endometriosis 2019
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