Role of cytokines in pathogenesis of endometriosis.

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This review summarizes current knowledge on how various cytokines contribute to the development of endometriosis by affecting immune surveillance and ectopic endometrial cell implantation and proliferation.

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Abstract

Sampson's theory stating that endometrial cells and fragments desquamate during the menstrual period are transported through Fallopian tubes into the peritoneal cavity where they implant, proliferate and develop into endometriotic lesions is generally accepted [1]. Accumulating data suggest that deficient immunity against retrograde endometrium during menstruation may be involved in the pathophysiology of endometriosis. Recent studies in women with endometriosis have demonstrated functional changes in several immunologic components in the peritoneal fluid as well as in sera of those patients. It was shown, for instance, that a wide pattern of cytokines are involved during endometrial cells implantation, proliferation and forming of endometriotic lesions. Those factors play a critical role in decreased immunologic surveillance, recognition and destruction of ectopic endometrial cells and possible facilitation of the implantation of ectopic endometrial tissues. The present review summarises the current knowledge on the role of different cytokines in the pathophysiology of endometriosis.

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Condition tags

endometriosis

MeSH descriptors

Cytokines Endometriosis Ascitic Fluid Ascitic Fluid Chemokine CCL5 Chemokine CCL5 Cytokines Endometriosis Endometriosis Endometriosis Endothelial Growth Factors Endothelial Growth Factors Epidermal Growth Factor Epidermal Growth Factor Female Humans Interleukin-12 Interleukin-12 Interleukin-6 Interleukin-6

Citation neighborhood

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

Cited by (37)

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europepmc
last seen: 2026-06-17T06:13:18.893374+00:00
openalex
last seen: 2026-06-10T17:14:06.276822+00:00
pubmed
last seen: 2026-05-13T22:13:30.513821+00:00
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