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Published on: January 6, 2012
Immunosuppressive activity of peritoneal fluid in women with endometriosis
D J Oosterlynck1, C Meuleman, M Waer
1Rega Institute for Medical Research, University of Leuven, Belgium.
Insights
Peritoneal fluid from women with endometriosis suppresses natural killer (NK) cell activity, potentially contributing to endometriosis pathogenesis. The immunosuppressive factor differs between peritoneal and follicular fluids.
Area of Science:
- Immunology
- Reproductive Biology
- Gynecology
Background:
- Endometriosis is associated with altered immune function.
- Peritoneal fluid and follicular fluid contain factors that can modulate immune responses.
Purpose of the Study:
- To investigate the immunosuppressive effects of peritoneal and follicular fluids on natural killer (NK) cell cytotoxicity and lymphocyte proliferation.
- To compare these effects in women with and without endometriosis.
Main Methods:
- Peritoneal and follicular fluids from women with endometriosis and controls were used to pre-treat lymphocytes.
- NK cell-mediated cytotoxicity against K562 tumor cells was measured.
- Phytohemagglutinin-induced lymphocyte proliferation was assessed.
Main Results:
- Peritoneal fluid from women with endometriosis significantly suppressed NK cell activity and lymphocyte proliferation compared to fertile controls.
- The immunosuppressive effect was more pronounced with longer incubation periods.
- The inhibitory factor in peritoneal fluid was not removed by charcoal treatment, unlike in follicular fluid.
Conclusions:
- Peritoneal fluid from women with severe endometriosis suppresses NK cell activity, suggesting a role in endometriosis pathogenesis.
- The immunosuppressive factors in peritoneal fluid and follicular fluid are distinct.
Objective:
To investigate the immunosuppressive effect of peritoneal fluid and follicular fluid on both natural killer-mediated cytotoxicity and phytohemagglutinin-induced lymphocyte proliferation.
Methods:
The peritoneal fluid of women with endometriosis was compared to both fertile and infertile control fluids. Lymphocytes were pretreated for 2 or 20 hours with peritoneal or follicular fluids, and their cytotoxicity toward K562 tumor cells was measured. We also investigated the phytohemagglutinin-induced stimulation of lymphocytes cocultured with peritoneal or follicular fluid.
Results:
Peritoneal fluid from women with endometriosis had a significantly greater immunosuppressive effect on natural killer-mediated cytotoxicity and on phytohemagglutinin stimulation of lymphocytes compared to peritoneal fluid of fertile women without endometriosis (P < .01 and P < .05, respectively). Using the peritoneal fluid of infertile women without endometriosis, these differences were significant only when compared to women with severe endometriosis. Inhibition of the natural killer activity increased when the incubation period was prolonged from 2 to 20 hours (P < .04). There was no correlation between the immunosuppressive effect of peritoneal fluid and the volume of peritoneal fluid, the day of the menstrual period, or estradiol, progesterone, prostaglandin E2, or prostaglandin F2 alpha levels. In peritoneal fluid, the factor responsible for inhibition of natural killer activity was not removed with charcoal treatment. In follicular fluid, on the other hand, the inhibition of natural killer activity decreased significantly after treatment with charcoal.
Conclusion:
Natural killer activity is suppressed by the peritoneal fluid of women with severe endometriosis; this may be important in the pathogenesis of endometriosis. The factor responsible for the inhibition of natural killer activity in peritoneal fluid is different from that in follicular fluid.
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