2009, Number 2
Next >>
Alerg Asma Inmunol Pediatr 2009; 18 (2)
The modulation of the synthesis of IL-2 an IFN-γ by means of human mononuclear cells is associated at the physiologic immunosuppression of the epididymal fluid
Rodríguez-Orozco AR, Mallea SLE, Machado CAJ, Cabrera OV, Carbonell VMA
Language: Spanish
References: 24
Page: 39-46
PDF size: 102.77 Kb.
ABSTRACT
Background and objective: IL-2 and IFN-γ play an important role in lymphocyte proliferation and activation. This study was undertaken to analyze if the inhibitory effect of the epididymal fluid on the immune response is associated with the modulation of the expression of IL-2 and IFN-γ.
Material and methods: Mononuclear cells (
Ficoll-paque d = 1.077) were isolated from blood from healthy donors and they were stimulated with epididymal fluid from everyone: an organ donor, and a man who was castrated by surgery. Once demonstrated the inhibition of proliferation of mononuclear cells, the levels of IL-2 and IFN-γ was determined by ELISA in supernatants of cultures of mononuclear cells stimulated with epididymal fluid and the results were expressed as inhibition or stimulation index.
Results: The inhibitory effect of the epididymal fluid on the mononuclear cells proliferation was not associated with the source of the epididymus and it was associated with potent stimulation of the synthesis of IFN-γ up to 51.6 x 10
3% in cells treated with 1/4 dilution of the epididymal fluid and with IL-2 synthesis inhibition up to 100% in cells treated with 1/4 dilution of the epididymal fluid.
Conclusions: The modulation of the synthesis of IL-2 and IFN-γ is one of the mechanisms involved in the inhibition of the local immune response by epydidimal substances.
REFERENCES
O’Rand MG, Romrell LJ. Appearance of cell surface auto and isoantigens during spermatogenesis in the rabbit. Rev Biol 1997; 55: 246-58.
Alexander NJ, Anderson DJ. Immunology of semen. Fertil Steril 1987; 47: 192-96.
Anderson DJ, Tarter TH. Immunosuppressive effects of mouse seminal plasma components “in vivo” e “in vitro”. J Immunol 1982; 128: 535-39.
Frenette G, Legare C, Saez F, Sullivan R. Macrophage migration inhibitory factor in the human epididymis and semen. Mol Hum Reprod 2005; 11: 575-82.
Kocak I, Dundar M, Yenisey C, Serter M, Gunaydin G. Pro-inflammatory cytokine response of the fluid contents of spermatoceles and epididymal cysts. Androl 2002; 34: 112-15.
Evaluation of the cytokines in genital secretions of patients with chronic prostatitis. Arch Ital Urol Androl 2003; 75: 179-86.
Catalog R&D System. Minneapolis, 1995.
Cytokine Bulletin. Spring 1995. R&D System. Minneapolis, 1995.
Bradford MM. A rapid and sensitive method for the quantitation of microgram quantitaties of proteins utilizing the principle of protein dye binding. Analytical Biochem 1976; 72: 248-254.
Sterzl I, Hampl R, Hill M, Hrda P, Matucha P. Immunomodulatory cytokines in human seminal plasma correlate with immunomodulatory steroids. Steroids 2003; 68: 725-31.
Jarvis JN, Zhao L, Moore HT, Long PM, Vani Gutta P. Regulation of cytokine in RNA expression by human choriocarcinoma JAR cell. Cell Immunol 1996; 168: 251-257.
Riccioli A, Starace D, D´Alessio A, Starac G, Padula F, De Cesaris P et al. TNF-alpha and IFN-gamma regulate expression and function of the Fas system in the seminiferous epithelium. J Immunol 2000; 165(2): 743-9.
Oyaizu N, McCloskey TW, Than S, Hu R, Kalyanaraman VS, Pahwa S. Cross-linking of CD4 molecules up regulates Fas antigen expression in lymphocytes by inducing IFN-g and tumor TNF-a secretion. Blood 1994; 84: 2622-25.
Arase H, N Arase; T Saito. IFN-g production by Natural Killer (NK) cells and NK 1.1 + T cells upon NKR-P1 cross-linking. J Exp Med 1996; 183: 2391-96.
Channon JY, LH Kasper. Toxoplasma gondii induced immune suppression by human peripheral blood monocytes. Role of IFN-g. Infect Immunol 1996; 64: 1181-89.
Carson WE, Ross ME, Baiocchi RA, Marien MJ, Boiani N, Grabstein K et al. Endogenous production of interleukin 15 by activated human monocytes is critical for optimal production of IFN-g by natural killer cells in vitro. J Clin Invest 1995; 96: 2575-92.
Novelli F, Bernabe P, Ozmen L, Rigomonti L, Allione A, Pestka S et al. Switching on of the proliferation or apoptosis of activated human T lymphocytes by IFN-g is correlated with the differential expression of the alfa and beta chains of its receptor. J Immunol 1996; 157: 1938-43.
Pernis A, Gupta S, Gollob KJ, Garfein E, Coffman KI, Schindler C et al. Lack of IFN-g receptor b-chain and the prevention of IFN-g signalling in Th1 cells. Science 1995; 269: 245-49.
Bach EA, Szabo SJ, Dighe AS, Ashkenazi A, Aquet M, Murphy KM et al. Ligand-induced autoregulation of IFN-g receptor b-chain expression in T helper cells subsets. Science 1995; 270: 1215-18.
Smith KA. Cytokines in the nineties. Eur Cytokine Net 1990; 1: 7-10.
Alderson MR, Armitage RJ, Marakowski E, Tough TW, Roux E, Schooley K et al. Fas transduces activation signals in normal human T lymphocytes. J Exp Med 1993; 178: 2231-36.
Liu Y, CA Janeway. IFN-g plays a critical role in induced cell death of effector T cell: a possible third mechanism of self tolerance. J Exp Med 1988; 172: 1735-39.
Novelli F, Di Pierro F, Francia Di Celle P, Bertini S, Affadicati P, Garotta G et al. Environmental signals influencing expression of the IFN-g receptor on human T cells control whether IFN-g promotes proliferation or apoptosis. J Immunol 1994; 152: 496-501.
Kishimoto HC, Surb D, Sprent J. Upregulation of surface markers on dying thymocytes. J Exp Med 1995; 181: 649-652.