Cited by 317Endometriosis Research and TreatmentReproductive System and PregnancyEctopic Pregnancy Diagnosis and Management

The role of cytokines in endometriosis

Wu, Ming‐Yih, Ho, Hong‐Nerng·2003·American Journal of Reproductive Immunology

Abstract

PROBLEM: To review the literature on the role of peritoneal cytokines in the pathogenesis and endometriosis-related infertility. METHODS OF STUDY: A MEDLINE search was conducted by the key words of cytokine and endometriosis in the English publications, and references identified within the identified papers were also reviewed. RESULTS: Several cytokines including interleukin (IL)-1, 6, 8, 10, tumor necrosis factor (TNF)-alpha, and vascular endothelial growth factor (VEGF) were reported to be increased in the peritoneal fluid (PF) of women with endometriosis. Those cytokines may be involved in macrophage activation, inflammatory change and enhanced angiogenesis. However, some cytokines were less expressed such as IL-2, and interferon (IFN)-gamma. They reflect the impaired T- and natural killer (NK)-cell function. Endometriotic implants produce some factors, e.g. matrix metalloproteinases (MMPs), Bcl-2, and affect their capacity to implant into the peritoneum. CONCLUSION: Peritoneal cytokines, which are produced by mesothelial cells, leukocytes and ectopic endometrial cells, interwork locally and systemically in women with endometriosis. More studies about the specific role and interactions of these cytokines are needed to improve the understanding of endometriosis and to develop novel therapies.

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Crossref · 10.1034/j.1600-0897.2003.01207.x

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  • Pelvic endometriosis is associated with a low-grade inflammation of the peritoneal cavity with higher concentrations of activated macrophages and thus with higher concentrations of many different cytokines and angiogenic factors.

    “Pelvic endometriosis is associated with a low-grade inflammation of the peritoneal cavity with higher concentrations of activated macrophages and thus with higher concentrations of the many different cytokines (68-72) and angiogenic factors (73)(74)(75)(76)(77)(78)(79)(80)(81)(82)(83)(84)(85)(86)(87)(88)(89)(90)(91).”

    From Pathogenesis of deep endometriosis (2017) · cites this paper as [71]

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Authors
Wu, M., & Ho, H.
Affiliations
National Taiwan University (TW)
Corresponding author
Ho, Hong‐Nerng
Venue
American Journal of Reproductive Immunology
Publisher
Wiley
Published
2003-04-09
Volume
49
Issue
5
Pages
285-296
ISSN
  • 0271-7352 (ISSN-L)
  • 1046-7408
  • 1600-0897
OpenAlex
W1992372603
Cited by
317
References
150
Citations by year
2026: 7 · 2025: 8 · 2024: 8 · 2023: 19 · 2022: 14 · 2021: 14 · 2020: 9 · 2019: 4 · 2018: 12 · 2017: 10 · 2016: 16 · 2015: 18 · 2014: 15 · 2013: 22 · 2012: 19
FWCI
2.72
Type
journal article
Language
en
Open access
closed
Locations
  • American Journal of Reproductive Immunology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Reproductive Medicine › Endometriosis Research and Treatment
  • Life Sciences › Immunology and Microbiology › Immunology › Reproductive System and Pregnancy
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Ectopic Pregnancy Diagnosis and Management
Keywords
endometriosis, cytokines, peritoneal fluid, endometriosis-associated infertility, interleukins, TNF-α, vascular endothelial growth factor, angiogenesis, macrophage activation, T cell function, natural killer cells, matrix metalloproteinases, Bcl-2, mesothelial cells
MeSH terms
Cell Adhesion, Endometriosis, Female, Humans, Infertility, Female, Neovascularization, Pathologic, Cytokines

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