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Published on: January 6, 2012
Altered interleukin-6 production by peritoneal leukocytes from patients with endometriosis
S E Rier1, A K Parsons, J L Becker
1Department of Medical Microbiology and Immunology, University of South Florida College of Medicine, Tampa 33606.
Insights
Interleukin-6 (IL-6) is present in peritoneal fluid in endometriosis patients. Peritoneal leukocytes show altered IL-6 production based on disease severity, suggesting a role in endometriosis pathophysiology.
Area of Science:
- Reproductive immunology
- Gynecologic pathology
Background:
- Interleukin-6 (IL-6) is a key cytokine implicated in inflammatory processes.
- Its role in the pathophysiology of endometriosis, a chronic inflammatory condition, requires further elucidation.
Purpose of the Study:
- To investigate the in vitro production of IL-6 by peritoneal leukocytes.
- To determine the presence of IL-6 in peritoneal fluid (PF) in vivo.
Main Methods:
- Peritoneal leukocytes were obtained from women undergoing laparoscopy for pain, infertility, or tubal ligation.
- Leukocyte IL-6 production was assessed spontaneously and after stimulation.
- IL-6 levels in peritoneal fluid were quantified.
Main Results:
- Peritoneal leukocytes from women with mild endometriosis or adhesions produced higher spontaneous levels of IL-6 compared to controls and severe endometriosis.
- Leukocytes from all endometriosis groups were unresponsive to endotoxin stimulation.
- Bioactive IL-6 was detected in the peritoneal fluid of all study groups.
Conclusions:
- IL-6 is present in the peritoneal fluid of women with and without endometriosis.
- Peritoneal leukocyte IL-6 production varies with endometriosis stage.
- Altered IL-6 production by leukocytes may contribute to endometriosis development and progression.
Objectives:
To investigate the ability of peritoneal leukocytes to produce interleukin-6 (IL-6) in vitro and to determine whether IL-6 is present in the peritoneal fluid (PF) in vivo.
Design:
Peritoneal leukocytes were assessed for spontaneous versus stimulated IL-6 production. Interleukin-6 in the PF was also quantitated.
Setting:
Leukocytes were recovered from PF obtained at the time of diagnostic laparoscopy for pain and infertility or from women undergoing bilateral tubal ligation.
Patients:
The study population included a total of 24 women. Experimental groups consisted of women undergoing tubal ligations (n = 6), patients with postinflammatory pelvic adhesions unrelated to endometriosis (n = 6), and women with minimal to mild endometriosis (n = 6), or moderate to severe disease (n = 6).
Results:
Peritoneal leukocytes from normal control women and patients with severe endometriosis spontaneously produced low levels of IL-6. In contrast, cells from women with mild disease or adhesions spontaneously released twofold to fourfold higher levels of this cytokine. Peritoneal leukocytes from patients with both mild and severe endometriosis were refractory to additional cytokine release directly in response to stimulation with endotoxin. Bioactive IL-6 was present in the PF of all patient groups, whereas immunoreactive IL-6 was not detected in this fluid.
Conclusions:
These data demonstrate that IL-6 was present in the PF of all patient groups. However, the ability of peritoneal leukocytes to produce IL-6 in vitro differed according to stage of disease. We hypothesize that altered leukocyte IL-6 production in vivo may contribute to the pathophysiology of endometriosis.
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