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Inhibition of Con A-induced lymphocyte proliferation by peritoneal exudate of Toxoplasma gondii-infected mice
H W Nam,* and W Y Choi
Department of Parasitology, Catholic University Medical College, Seoul 137-107, Korea.
Received July 21, 1995; Accepted August 11, 1995.
Abstract
The presence of biological response modifiers (BRM)-like effect was confirmed in peritoneal exudate (PE) of Toxoplasma gondii-infected ICR mice which inhibited Concanavalin A (Con A)-induced peritoneal lymphocyte (PL) proliferation. During 5 days of PL incubation with 10 µg/ml Con A with or without PE, 3H-thymidine uptake was measured for the last 24 hrs. Compared to uninduced control, PL proliferated by 7.3-fold with Con A induction. When PE of infected mice was added, PL proliferation was inhibited by 74.0 ± 11.9% whereas inhibition by PE of normal mice was 16.4 ± 8.3%. Inhibitory effect of PE increased exponentially from 3 days up to 4-5 days of survival after the infection. Inhibitory activity of PE was decreased concentration- dependently. Also the inhibition was diminished when the PE was treated with heat of 95℃ for 10 min or precipitated with 10% trichloracetic acid (TCA). In SDS-PAGE of PE, many minor bands appeared newly. Heat-labile protein molecule in PE exerted inhibitory activity to Con A-induced lymphocyte proliferation.
Figures
Fig. 1 Inhibition of Con A-induced peritoneal lymphocyte (Pl) proliferation by peritoneal exudate of mice infected with T. gondii. Control, PL only; Con A, PL induced with Con A; Con A + PE, PL induced with Con A in the presence of peritoneal exudate; and PE, PL without Con A but with peritoneal exudate.
Fig. 2 Percent inhibition of Con A-induced proliferation by PE from infected and non-infected mice. Percent inhibition was calculated by the formula: (1-cpm of PL with Con A and PE/ cpm of PL with Con A) ×100. PE (infected), PE from infected mice; and PE (Normal), PE from non-infected mice.
Fig. 3 Changing pattern of inhibitory effects on Con A-induced PL proliferation in PE which were collected consecutively after peritoneal infection with T. gondii.
Fig. 4 Effect of PE dilution on inhibition of Con A-induced PL proliferation. PE added to the culture well was 10% (v/v) of media primarily, the dilution factors were further multiplied by 10 actually.
Fig. 5 SDS-PAGE pattern of PE on the time course of postinfection. M, molecular weight markers; N, PE of uninfected normal mouse, and 1-4, day after infection.
Fig. 6 Effects heat (95℃ for 10 min) and 10% TCA precipitation on inhibition of Con A-induced PL proliferation.
References
1.
Albina JE, Abate JA, Henry WL Jr. Nitric oxide production is required for murine resident peritoneal macrophages to suppress mitogen-stimulated T cell proliferation. Role of IFN-gamma in the induction of the nitric oxide-synthesizing pathway. J Immunol 1991;147(1):144–148.
2.
Alleva DG, Burger CJ, Elgert KD. Tumor-induced regulation of suppressor macrophage nitric oxide and TNF-alpha production. Role of tumor-derived IL-10, TGF-beta, and prostaglandin E2. J Immunol 1994;153(4):1674–1686.
3.
Allison AC. Immunol Res 1978;40:3–27.
4.
Chan J, Siegel JP, Luft BJ. Demonstration of T-cell dysfunction during acute toxoplasma infection. Cell Immunol 1986;98(2):422–433.
5.
Ding L, Linsley PS, Huang LY, Germain RN, Shevach EM. IL-10 inhibits macrophage costimulatory activity by selectively inhibiting the up-regulation of B7 expression. J Immunol 1993;151(3):1224–1234.
6.
Gazzinelli RT, Oswald IP, James SL, Sher A. IL-10 inhibits parasite killing and nitrogen oxide production by IFN-gamma-activated macrophages. J Immunol 1992;148(6):1792–1796.
8.
Isobe K, Nakashima I. Feedback suppression of staphylococcal enterotoxin-stimulated T-lymphocyte proliferation by macrophages through inductive nitric oxide synthesis. Infect Immun 1992;60(11):4832–4837.
9.
Kim SE, et al. Korean J infect Dis 1993;25:63–69.
11.
Kung JT, Brooks SB, Jakway JP, Leonard LL, Talmage DW. Suppression of in vitro cytotoxic response by macrophages due to induced arginase. J Exp Med 1977;146(3):665–672.
12.
Lowenberg B, van Gijn J, Prins E, Polderman AM. Fatal cerebral toxoplasmosis in a bone marrow transplant recipient with leukemia. Transplantation 1983;35(1):30–34.
13.
Luft BJ, Pedrotti PW, Engleman EG, Remington JS. Induction of antigen-specific suppressor T cells during acute infection with Toxoplasma gondii. J Infect Dis 1987;155(5):1033–1037.
Mellors JW, Debs RJ, Ryan JL. Incorporation of recombinant gamma interferon into liposomes enhances its ability to induce peritoneal macrophage antitoxoplasma activity. Infect Immun 1989;57(1):132–137.
16.
Metzger Z, Hoffeld JT, Oppenheim JJ. Macrophage-mediated suppression I Evidence for participation of both hdyrogen peroxide and prostaglandins in suppression of murine lymphocyte proliferation. J Immunol 1980;124(2):983–988.
18.
Murray HW, Scavuzzo D, Jacobs JL, Kaplan MH, Libby DM, Schindler J, Roberts RB. In vitro and in vivo activation of human mononuclear phagocytes by interferon-gamma. Studies with normal and AIDS monocytes. J Immunol 1987;138(8):2457–2462.
19.
Sharma SD, Hofflin JM, Remington JS. In vivo recombinant interleukin 2 administration enhances survival against a lethal challenge with Toxoplasma gondii. J Immunol 1985;135(6):4160–4163.
Suzuki Y, Orellana MA, Schreiber RD, Remington JS. Interferon-gamma: the major mediator of resistance against Toxoplasma gondii. Science 1988;240(4851):516–518.
23.
Sypek JP, Jacobson S, Vorys A, Wyler DJ. Comparison of gamma interferon, tumor necrosis factor, and direct cell contact in activation of antimycobacterial defense in murine macrophages. Infect Immun 1993;61(9):3901–3906.
24.
Unanue ER, Allen PM. The basis for the immunoregulatory role of macrophages and other accessory cells. Science 1987;236(4801):551–557.
25.
Yano A, Norose K, Yamashita K, Aosai F, Sugane K, Segawa K, Hayashi S. Immune response to Toxoplasma gondii--analysis of suppressor T cells in a patient with symptomatic acute toxoplasmosis. J Parasitol 1987;73(5):954–961.