The involvement of T lymphocytes in the pathogenesis of endometriotic tissues overgrowth in women with endometriosis

Mediators of Inflammation

Volumn 12, Issue 3, 2003, Pages 131-138

  Szyllo, Krzysztof ^a   Tchorzewski, Henryk ^a,b   Banasik, Malgorzata ^a   Glowacka, Ewa ^a   Lewkowicz, Przemyslaw ^a   Kamer Bartosinska, Anna ^a  

^a POLISH MOTHER S MEMORIAL HOSPITAL RESEARCH INSTITUTE   (Poland)

^b MEDICAL UNIVERSITY OF LODZ   (Poland)

Author keywords

Diminished IFN production; Endometriosis; Increased IL 4 production; NK cells; T regulatory cells

Indexed keywords

CD4 ANTIGEN; CD8 ANTIGEN; CYTOKINE; GAMMA INTERFERON; GONADORELIN; GOSERELIN; INTERLEUKIN 10; INTERLEUKIN 12; INTERLEUKIN 2; INTERLEUKIN 4; INTERLEUKIN 6; PHYTOHEMAGGLUTININ; TUMOR NECROSIS FACTOR ALPHA;

ADULT; AGE; ANTIGEN DETECTION; ANTIINFLAMMATORY ACTIVITY; ARTICLE; CELL PROLIFERATION; CELLULAR DISTRIBUTION; COMPUTER PROGRAM; CONTROLLED STUDY; CONVALESCENCE; CYTOKINE PRODUCTION; DISEASE CLASSIFICATION; ENDOMETRIOSIS; ENDOMETRIUM; ENDOMETRIUM HYPERPLASIA; FEMALE; FEMALE FERTILITY; FISHER EXACT TEST; HORMONAL THERAPY; HUMAN; HYPOTHESIS; IMMUNOREGULATION; INTERFERON PRODUCTION; LAPAROSCOPY; LYMPHOCYTE ACTIVATION; LYMPHOCYTE FUNCTION; MACROPHAGE; MACROPHAGE FUNCTION; MAJOR CLINICAL STUDY; MONOCYTE; NATURAL KILLER CELL; PATHOGENESIS; PERIPHERAL CIRCULATION; PERITONEAL FLUID LEVEL; PHENOTYPE; PRIORITY JOURNAL; SCORING SYSTEM; STATISTICAL ANALYSIS; STUDENT T TEST; T LYMPHOCYTE; T LYMPHOCYTE SUBPOPULATION; TISSUE GROWTH;

ADULT; ASCITIC FLUID; CD4-CD8 RATIO; CYTOKINES; ENDOMETRIOSIS; ENDOMETRIUM; FEMALE; GOSERELIN; HUMANS; INFLAMMATION MEDIATORS; INTERFERON TYPE II; INTERLEUKIN-4; KILLER CELLS, NATURAL; LAPAROSCOPY; LYMPHOCYTE COUNT; MIDDLE AGED; T-LYMPHOCYTES;

MARTES PENNANTI;

EID: 0038779947     PISSN: 09629351     EISSN: None     Source Type: Journal    
DOI: 10.1080/0962935031000134842     Document Type: Article

References (24)

1. Hornung D, Klingel K, Dohrn K, Kandolf R, Wallwiener D, Taylor RN. Regulated on activation, normal T-cell-expressed and secreted mRNA expression in normal endometrium and endometriotic implants: assessment of autocrine/paracrine regulation by in situ hybridization. Am J Pathol 2001; 158: 1949-1954.
2. Chatenoud L, Salomon B, Bluestone JA. Suppressor T cells - they're back and critical for regulation of autoimmunity! Immunol Rev 2001; 182: 149-163.
3. Arima K, Nasu K, Narahara H, Fujisawa K, Matsui N, Miyakawa I. Effect of lipopolysaccharide and cytokines on production of Rantes by cultured human endometrial stromal cells. Mol Hum Reprod 2000; 6: 246-251.
4. Zeyneloglu HB, Senturk LM, Seli E, Bahtiyar OM, Olive DL, Arici A. The peritoneal fluid levels of interleukin-12 in women with endometriosis. Am J Reprod Immunol 1998; 39: 152-156.
5. Hoeger KM, Guzick DS. An update on the classification of endometriosis. Clin Obstet Gynecol 1999; 42: 611-619.
6. Buckley CD, Pilling D, Lord Janet M, Akbar Arne N, Scheel-Toellner D, Salmon M. Fibroblasts regulate the switch from acute resolving to chronic persistent inflammation. Trend Immunol 2001; 22: 199-204.
7. Hogaboam CM, Bone-Larson CL, Lipinski S, Lukacs NW, Chensue SW, Strieter RM, Kunkel SL. Differential monocyte chemoattractant protein-1 and chemokine receptor 2 expression by murine lung fibroblasts derived from Th1-and Th2-type pulmonary granuloma models. J Immunol 1999; 163: 2193-2201.
8. Keenan A, Chen TT, Chadwell NL, Torry DS, Caudle MR. Interferon-gamma (IFN-γ) and interleukin-6 (IL-6) in peritoneal fluid and macrophage-conditioned media of women with endometriosis. Amer J Reprod Immunol 1994; 32: 180-183.
9. Ho HN, Wu MY, Yang YS. Peritoneal cellular immunity and endometriosis. Amer J Reprod Immunol 1997; 38: 400-412.
10. Ho HN, Wu MY, Chao KH, et al. Decrease in interferon gamma production and impairment of T-lymphocyte proliferation in peritoneal fluid of women with endometriosis. Am J Obstet Gynecol 1996; 175: 1236-1241.
11. Oosterlynck DJ, Lacquer FA, Mear WM, Koninclcx PR. Lymphokine-activated killer activity in women with endometriosis. Gynecol Obstet Invest 1994; 37: 185-190.
12. Hsu CC, Yang BC, Wu MH, Huang KE. Enhanced interleukin-4 expression in patients with endometriosis. Fertil Steril 1997; 67: 1059-1064.
13. Mangan DF, Robertson B, Wahl SM. IL-4 enhances programmed cell death (apoptosis) in stimulated human monocytes. J Immunol 1992; 148: 1812-1816
14. Vigano P, Vercellini P, Di Blasio AM, Colombo A, Candiani GB, Vignali M. Deficient antiendometrium lymphocyte-mediated cytotoxicity in patients with endometriosis. Fertil Steril 1991; 56: 894-899.
15. Miossec P, Banchereau J. Interleukin 4: a potential antitumor and antiinflammatory agent. In: Oppenheim J, Rossio JL, Gearing AJH, eds. Clinical Applications of Cytokines, Oxford: Oxford University Press, 1993: 171-176.
16. Kadowaki N, Antonenko S, Lau JY, Liu YJ. Natural interferon alpha/beta-producing cells link innate and adaptive immunity. J Exp Med 2000; 192: 219-226.
17. Hsu CC, Lin YS, Wang St, Huang KE. Immunomodulation in woman with endometriosis receiving GnRH agonist. Obstet Gynecol 1997; 89: 993-998.
18. Wu MY, Yang JH, Chao KH, Hwang JL, Yang YS, Ho HN. Increase in the expression of killer cell inhibitory receptors on peritoneal natural killer cells in women with endometriosis. Fertil Steril 2000; 74: 187-1191.
19. Tchorzewski H, Krasomski G, Biesiada L, Glowacka E, Banasik M, Lewkowicz P. IL-12, IL-6 and IFN-γ production by lymphocytes of pregnant women with rheumatoid arthritis remission during pregnancy. Mediat Inflamm 2000; 9: 289-293.
20. Gleicher N, Dmowski WP, Siegel I. Lymphocyte subsets in endometriosis. Obstet Gynecol 1984; 63: 463-466.
21. Klentzeris LD, Bulmer JN, Liu DT, Morrison L. Endometrial leukocyte subpopulations in women with endometriosis. Eur J Obstet Gynecol Reprod Biol 1995; 63: 41-47.
22. Belardelli F, Ferrantini M. Cytokines as a link between innate and adaptive antitumor immunity. Trends Immunol 2002; 23: 201-208.
23. Tchórzewski H, Glowacka E, Banasik M, Lewkowicz P, Szalapska Zawodniak M. Activated T lymphocytes from patiens with high risk of type I diabetes mellitus have different ability to produce interferon-γ, interleukin-6 and interleukin 10 and undergo anti-CD95 induced apoptosis after insulin stimulation. Immunol Lett 2001; 75: 225-234.
24. Glowacka E, Banasik M, Lewkowicz P, Tchórzewski H. The effect of LPS on neutrophils from patients with high risk of type I diabetes mellitus in relation to IL-8, IL-10 and IL-12 production and apoptosis in vitro. Scand J Immunol 2002; 55: 210-217.