期刊
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY
卷 76, 期 4, 页码 292-298出版社
WILEY
DOI: 10.1111/aji.12552
关键词
dienogest; endometriosis; inflammation; medroxyprogesterone acetate; norethisterone acetate
资金
- Swiss National Science Foundation [320030_140774/1]
- Swiss National Science Foundation (SNF) [320030_140774] Funding Source: Swiss National Science Foundation (SNF)
Problem: Endometriosis is an estrogen-dependent inflammatory disease. Progestins are a first-line treatment for endometriosis via activation of pituitary progesterone receptors and suppression of systemic estrogen: a less than optimal treatment. Increasing evidence is beginning to show that progestins may also influence local endometriotic cells, which may contribute to their clinical efficacy. Method of study: Endometrial stromal cells (ESC) isolated from women with endometriosis were cultured with TNF-alpha to simulate an inflammatory environment. ESC were treated with the progestins, medroxyprogesterone acetate (MPA), norethisterone acetate (NETA), or dienogest (DNG) and cytokine mRNA production, protein secretion, and cell viability measured. Results: DNG, NETA, and MPA suppressed the secretion of interleukin (IL)-6, IL-8, and monocyte chemotactic protein (MCP)-1 from ESC. DNG and NETA only reduced the TNF-alpha-stimulated mRNA production. All three progestins suppressed TNF-alpha-stimulated ESC proliferation. Conclusion: Progestins may influence endometriotic stromal cells altering the inflammatory microenvironment and their clinical efficacy.
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