Intraperitoneal recombinant interleukin-2 activates leukocytes in rat endometriosis

• Published in: Journal of reproductive immunology 2007-06, Vol.74 (1), p.124-132
• Main Authors: Velasco, Irene, Quereda, Francisco, Bermejo, Rosa, Campos, Adolfo, Acién, Pedro
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Double-Blind Method; Embryology: invertebrates and vertebrates. Teratology; Endometriosis - drug therapy; Endometriosis - immunology; Experimental endometriosis; Female; Flow Cytometry; Fundamental and applied biological sciences. Psychology; IL-2; Immune modulator; Immunohistochemistry; Injections, Intraperitoneal; Interleukin-2 - administration & dosage; Interleukin-2 - immunology; Interleukin-2 - therapeutic use; Killer Cells, Natural - drug effects; Killer Cells, Natural - immunology; Leukocytes - drug effects; Leukocytes - immunology; Obstetrics and Gynecology; Random Allocation; Rat; Rats; Rats, Wistar; Recombinant Proteins - administration & dosage; Recombinant Proteins - therapeutic use
• ISSN: 0165-0378; 1872-7603
• DOI: 10.1016/j.jri.2006.12.001

Abstract The aim of this double-blinded study was to determine changes in leukocyte populations in blood, peritoneal lavage fluid, eutopic and ectopic endometrium after treatment with recombinant rat interleukin-2 (IL-2) using an in vivo experimental model of rat endometriosis. The in vivo model involved transplanting four square fragments of autologous endometrium onto the inner surface of the abdominal wall in 20 Wistar rats. The control group was constituted by 20 sham-operated rats. Both groups were randomly treated (1-month interval treatment) with 2 intraperitoneal doses of glucose solution (5%) that did or did not contain recombinant IL-2, and animals were sacrificed 4 weeks after the last dose of treatment. Blood and peritoneal lavage were obtained during the initial and final laparotomy, whereas eutopic and ectopic endometrium were collected at the end of the experiment. Endometriotic implants were measured in each laparotomy to determine any change in size. Leukocyte populations were analyzed by flow cytometry and immunofluorescence microscopy. Cytometric results were similar in blood and peritoneal lavage. CD25+ and natural killer (NK) cell levels in peripheral blood were lower in rats with endometriosis treated with IL-2, whereas NK cells increased in lavage compared to placebo group. The percentage of macrophages and dendritic cells in blood were higher in all rats treated with IL-2, as well as peritoneal dendritic cells. Implant size of these rats decreased significantly, showing a greater number of activated lymphocytes, macrophages, NK and dendritic cells inside them. In conclusion, recombinant IL-2 induced recruitment of activated leukocytes into endometriotic-like foci, and this was related to a reduction of the implant size, suggesting potential effectiveness of IL-2 as an immunomodulatory agent in this pathology.