The present study explored the possible relationships between immune cell subsets and interleukin (IL)-12 or IL-13 levels in the peritoneal fluid of patients with and without endometriosis. Peritoneal fluid samples were obtained from 80 women while they were undergoing laparoscopy for pain, infertility, tubal ligation or re-anastomosis. The American Fertility Society scoring system was used to determine the extension of endometriosis. The peritoneal fluid mononuclear cells were analyzed for immunophenotyping using cytometry, whereas peritoneal fluid concentrations of interleukins were measured using two ultrasensitive commercially available enzyme-linked immunosorbent assay kits. Significantly higher peritoneal fluid IL-12 levels were found in women with moderate or severe endometriosis (stages III and IV) than in healthy controls (p < 0.01). Conversely, subjects with endometriosis showed remarkably lower peritoneal fluid IL-13 concentrations than controls, independent of the severity of the disease (p < 0.05). Considering immune system effectors, patients with endometriosis presented a significantly higher peritoneal fluid CD8(+)/CD4(+) ratio when compared with healthy controls. Moreover, the number of peritoneal fluid CD8(+) and CD4(+) activated T cells was significantly lower in the former than in the latter group, independent of the endometriosis stage. Connections were observed between peritoneal fluid interleukins and peritoneal fluid T cells: both patients with endometriosis and controls presented an inverse correlation between peritoneal fluid activated T cells and IL-13 levels, and a direct correlation between peritoneal fluid T cells and IL-12 concentrations. These data seem to suggest that a reciprocal modulation exists between peritoneal fluid cytokines and T lymphocyte subsets in patients with endometriosis.
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Queen Mary Univ London, Reprod Physiol Lab, St Bartholomews Sch Med & Dent, London, England
London Bridge Fertil Gynecol & Genet Ctr, London, EnglandQueen Mary Univ London, Reprod Physiol Lab, St Bartholomews Sch Med & Dent, London, England
Gillott, David J.
Remorgida, Valentino
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San Martino Hosp, Dept Obstet & Gynecol, Genoa, Italy
Univ Genoa, Genoa, ItalyQueen Mary Univ London, Reprod Physiol Lab, St Bartholomews Sch Med & Dent, London, England
Remorgida, Valentino
Anserini, Paola
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San Martino Hosp, Dept Obstet & Gynecol, Genoa, Italy
Univ Genoa, Genoa, ItalyQueen Mary Univ London, Reprod Physiol Lab, St Bartholomews Sch Med & Dent, London, England
Anserini, Paola
Ragni, Nicola
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San Martino Hosp, Dept Obstet & Gynecol, Genoa, Italy
Univ Genoa, Genoa, ItalyQueen Mary Univ London, Reprod Physiol Lab, St Bartholomews Sch Med & Dent, London, England
Ragni, Nicola
Grudzinskas, Jurgis G.
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Queen Mary Univ London, Reprod Physiol Lab, St Bartholomews Sch Med & Dent, London, England
London Bridge Fertil Gynecol & Genet Ctr, London, EnglandQueen Mary Univ London, Reprod Physiol Lab, St Bartholomews Sch Med & Dent, London, England
机构:Univ Sao Paulo FMUSP SP, Sch Med, Endometriosis Unit, Dept Obstet & Gynaecol, Sao Paulo, Brazil
Pupo-Nogueira, A.
de Oliveira, R. M.
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机构:Univ Sao Paulo FMUSP SP, Sch Med, Endometriosis Unit, Dept Obstet & Gynaecol, Sao Paulo, Brazil
de Oliveira, R. M.
Petta, C. A.
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机构:Univ Sao Paulo FMUSP SP, Sch Med, Endometriosis Unit, Dept Obstet & Gynaecol, Sao Paulo, Brazil
Petta, C. A.
Podgaec, S.
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机构:Univ Sao Paulo FMUSP SP, Sch Med, Endometriosis Unit, Dept Obstet & Gynaecol, Sao Paulo, Brazil
Podgaec, S.
Dias, J. A., Jr.
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机构:Univ Sao Paulo FMUSP SP, Sch Med, Endometriosis Unit, Dept Obstet & Gynaecol, Sao Paulo, Brazil
Dias, J. A., Jr.
Abrao, M. S.
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Univ Sao Paulo FMUSP SP, Sch Med, Endometriosis Unit, Dept Obstet & Gynaecol, Sao Paulo, BrazilUniv Sao Paulo FMUSP SP, Sch Med, Endometriosis Unit, Dept Obstet & Gynaecol, Sao Paulo, Brazil