Natural Killer Cells: Key Players in Endometriosis

Thiruchelvam U, Uma Thiruchelvam, Mary Wingfield, Cliona O'Farrelly, Cliona O’Farrelly
American journal of reproductive immunology (New York, N.Y. : 1989) · 2015 · vol. 74(4) , pp. 291–301 · doi:10.1111/aji.12408 · PMID:26104509 · W2155024087
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This review examines evidence indicating that women with endometriosis exhibit impaired peripheral and peritoneal natural killer cell function, suggesting a potential role for abnormal uterine natural killer cells in disease pathogenesis and infertility.

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Abstract

Endometriosis affects more than 10% of women, causing significant pain and morbidity. It is also a significant cause of infertility. The aetiology of the disease remains an enigma, and the mechanisms responsible for the associated infertility are unclear. A role for immune cells in endometriosis has been postulated, with attention directed towards natural killer (NK) cells and macrophages. NK cells kill tumours and infected cells but also have roles in tissue remodelling in several organs including the uterus and are key to successful pregnancy. Here, we explore evidence (from peer-reviewed published articles) of phenotypic and functional abnormalities in NK cell subpopulations of women with endometriosis. It is clear that peripheral blood NK cells and peritoneal NK cells have reduced cytotoxic function in women with endometriosis. Uterine NK cells have a vital role in infertility, but very little research has been carried out in this area. We propose that abnormal u NK cell activity may contribute to the pathogenesis of endometriosis and its associated infertility and that future research should focus on this complex area.

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Condition tags

endometriosisinfertility

MeSH descriptors

Endometriosis Infertility, Female Killer Cells, Natural Animals Animals Chemokines Chemokines Chemokines Disease Models, Animal Disease Models, Animal Endometriosis Endometriosis Endometriosis Endometriosis Endometrium Endometrium Endometrium Endometrium Female Female

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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. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

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