Decrease in peripheral blood polymorphonuclear leukocyte chemotactic index in endometriosis: role of prostaglandin E2 release

Obstet Gynecol. 1998 Jan;91(1):25-9. doi: 10.1016/s0029-7844(97)00592-9.

Abstract

Objective: To investigate the effect of disease on peripheral blood polymorphonuclear leukocyte chemotactic index and natural killer cell cytotoxicity and to provide additional information concerning the cell-mediated immune function in endometriosis.

Methods: Chemotactic index of peripheral blood polymorphonuclear leukocytes, natural killer cell activity, and plasma estradiol (E2) and plasma prostaglandin (PG) E2 levels were evaluated in 46 women who underwent laparoscopy or laparotomy for pelvic pain, infertility, and/or benign adnexal masses.

Results: The 20 women (43%) with endometriosis showed a decrease in peripheral blood polymorphonuclear leukocyte chemotactic index, related to advanced disease stage (P < .001). A significant inverse correlation was observed between plasma PGE2 levels and chemotactic index in stage III and IV endometriosis (r = -.73, P = .004). Similarly, natural cytotoxicity was decreased significantly with respect to the stage of endometriosis (P = .004) and related inversely to plasma PGE2 levels (r = -.74, P = .003). A direct relationship was observed between PGE2 and plasma E2 levels (r = .59, P = .006).

Conclusion: Advanced endometriosis is associated with decreased peripheral blood polymorphonuclear leukocyte chemotactic index and natural killer cytotoxicity, which may be related to plasma PGE2 and E2 levels.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Chemotaxis, Leukocyte / immunology*
  • Cytotoxicity, Immunologic / immunology*
  • Diagnostic Techniques and Procedures
  • Dinoprostone / blood*
  • Endometriosis / blood
  • Endometriosis / immunology*
  • Endometriosis / pathology
  • Estradiol / blood*
  • Female
  • Humans
  • Killer Cells, Natural / immunology*
  • Neutrophils / immunology
  • Reference Values

Substances

  • Estradiol
  • Dinoprostone