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Cytotoxicity of lymphokine activated peritoneal macrophages against Trichomonas vaginalis
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Korean J Parasito > Volume 29(4):1991 > Article

Original Article
Korean J Parasitol. 1991 Dec;29(4):381-383. English.
Published online Mar 20, 1994.  http://dx.doi.org/10.3347/kjp.1991.29.4.381
Copyright © 1991 by The Korean Society for Parasitology
Cytotoxicity of lymphokine activated peritoneal macrophages against Trichomonas vaginalis
K Yoon,J S Ryu and D Y Min
Department of Parasitology, College of Medicine, Hanyang University, Seoul 133-791, Korea.
Abstract

Trichomonas vaginalis is a parasitic flagellate in the urogenital tract of human. Innate cytotoxicity of macrophages against T. vaginalis has been recognized, but any report on the cytotoxicity of lymphokine-activated macrophages to T. vaginalis is not yet available. The present study aimed to elucidate the lymphokine-activated cell mediated cytotoxic effect against T. vaginalis by mouse peritoneal macrophages. Cytotoxicity was measured by counting the release of 3H-thymidine from prelabeled protozoa, and tested in U-bottom microtiter plates. Nitrite concentration in culture supernatants was measured by standard Griess reaction.

The results obtained are as follows:

1. The cytotoxicity of macrophages was increased by addition of rIL-2 or rIFN-γ.

2. Cytotoxicity of macrophages was reduced by addition of rIL-4 to rGM-CSF, rIL-2 or rIFN-γ.

3. Crude lymphokine mixed with anti-IL-2 decreased the cytotoxicity of macrophages.

4. In case of macrophages cultured with rIFN-γ or rIL-4, the concentration of nitrite was related with cytotoxicity of macrophages against T. vaginalis, but the cytotoxicity of macrophages cultured with rIL-2 and rIFN-γ was decreased in spite of its high production of nitrite.

From the results obtained, it is assumed that rIL-2 and rIFN-γ enhance the cytotoxicity of macrophages while rIL-4 inhibits the cytotoxicity against T. vaginalis, and that the production of nitrite does not relate with the cytotoxicity of macrophages, but nitric oxide may play a role as an inhibitory factor on the proliferation of T. vaginalis.

Figures


Fig. 1
Cytotoxicity of macrophages activated by rGM-CSF against T. vaginalis.


Fig. 2
Cytotoxicity of macrophages activated by rIL-2 against T. vaginalis.


Fig. 3
Cytotoxicity of macrophages activated by rIFN-γ against T. vaginalis.


Fig. 4
Cytotoxicity of macrophages activated by rIL-4 against T. vaginalis.

Tables


Table 1
Cytotoxicity of macrophages activated by various concentration of recombinant lymphokine against T. vaginalis


Table 2
Cytotoxicity of recombinant lymphokine-activated macrophages against T. vaginalis


Table 3
Cytotoxicity of macrophages activated by combined recombinant lymphokine against T. vaginalis


Table 4
Effect of lymphokine activated macrophages on the proliferation of T. vaginalis


Table 5
Effect of various concentration of crude lymphokine and anti-lymphokine antibody on the cytotoxicity of macrophages against T. vaginalis

References
1. Adams LB, Hibbs JB Jr, Taintor RR, Krahenbuhl JL. Microbiostatic effect of murine-activated macrophages for Toxoplasma gondii. Role for synthesis of inorganic nitrogen oxides from L-arginine. J Immunol 1990;144(7):2725–2729.
 
2. Belosevic M, Davis CE, Meltzer MS, Nacy CA. Regulation of activated macrophage antimicrobial activities. Identification of lymphokines that cooperate with IFN-gamma for induction of resistance to infection. J Immunol 1988;141(3):890–896.
 
3. Belosevic M, Finbloom DS, Meltzer MS, Nacy CA. IL-2. A cofactor for induction of activated macrophage resistance to infection. J Immunol 1990;145(3):831–839.
 
4. Bout DT, Joseph M, David JR, Capron AR. In vitro killing of S. mansoni schistosomula by lymphokine-activated mouse macrophages. J Immunol 1981;127(1):1–5.
 
5. Ding AH, Nathan CF, Stuehr DJ. Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages. Comparison of activating cytokines and evidence for independent production. J Immunol 1988;141(7):2407–2412.
 
6. Diamond LS. Techniques of axenic cultivation of Entamoeba histolytica Schaudinn, 1903 and E. histolytica-like amebae. J Parasitol 1968;54(5):1047–1056.
  
7. Green SJ, Meltzer MS, Hibbs JB Jr, Nacy CA. Activated macrophages destroy intracellular Leishmania major amastigotes by an L-arginine-dependent killing mechanism. J Immunol 1990;144(1):278–283.
 
8. Golden JM, Tarleton RL. Trypanosoma cruzi: cytokine effects on macrophage trypanocidal activity. Exp Parasitol 1991;72(4):391–402.
  
9. Hageman RH, et al. Methods Enzymol 1980;69:270.
 
10. Hughes HP, Speer CA, Kyle JE, Dubey JP. Activation of murine macrophages and a bovine monocyte cell line by bovine lymphokines to kill the intracellular pathogens Eimeria bovis and Toxoplasma gondii. Infect Immun 1987;55(3):784–791.
 
11. James SL, Glaven J. Macrophage cytotoxicity against schistosomula of Schistosoma mansoni involves arginine-dependent production of reactive nitrogen intermediates. J Immunol 1989;143(12):4208–4212.
 
12. James SL, Hibbs JB Jr. The role of nitrogen oxides as effector molecules of parasite killing. Parasitol Today 1990;6(9):303–305.
  
13. James SL. The effector function of nitrogen oxides in host defense against parasites. Exp Parasitol 1991;73(2):223–226.
  
14. Landolfo S, Martinotti MG, Martinetto P, Forni G. Natural cell-mediated cytotoxicity against Trichomonas vaginalis in the mouse. I. Tissue, strain, age distribution, and some characteristics of the effector cells. J Immunol 1980;124(2):508–514.
 
15. Lehn M, Weiser WY, Engelhorn S, Gillis S, Remold HG. IL-4 inhibits H2O2 production and antileishmanial capacity of human cultured monocytes mediated by IFN-gamma. J Immunol 1989;143(9):3020–3024.
 
16. Lepoivre M, Boudbid H, Petit JF. Antiproliferative activity of gamma-interferon combined with lipopolysaccharide on murine adenocarcinoma: dependence on an L-arginine metabolism with production of nitrite and citrulline. Cancer Res 1989;49(8):1970–1976.
 
17. Liew FY, Millott S, Parkinson C, Palmer RM, Moncada S. Macrophage killing of Leishmania parasite in vivo is mediated by nitric oxide from L-arginine. J Immunol 1990;144(12):4794–4797.
 
18. Liew FY, et al. Parasitology Today 1991;7:A16–A21.
 
19. Mantovani A, Polentarutti N, Peri G, Martinotti G, Landolfo S. Cytotoxicity of human peripheral blood monocytes against Trichomonas vaginalis. Clin Exp Immunol 1981;46(2):391–396.
 
20. Olivier M, Bertrand S, Tanner CE. Killing of Leishmania donovani by activated liver macrophages from resistant and susceptible strains of mice. Int J Parasitol 1989;19(4):377–383.
  
21. Ryu JS, Ahn MH, Min DY. [Cytotoxicity of resident and lymphokine-activated mouse peritoneal macrophage against Trichomonas vaginalis]. Korean J Parasitol 1990;28(2):85–89.
 
22. Scott P, Pearce E, Cheever AW, Coffman RL, Sher A. Role of cytokines and CD4+ T-cell subsets in the regulation of parasite immunity and disease. Immunol Rev 1989;112:161–182.
  
23. Vincendeau P, Daulouede S. Macrophage cytostatic effect on Trypanosoma musculi involves an L-arginine-dependent mechanism. J Immunol 1991;146(12):4338–4343.
 
24. Wahl SM, McCartney-Francis N, Hunt DA, Smith PD, Wahl LM, Katona IM. Monocyte interleukin 2 receptor gene expression and interleukin 2 augmentation of microbicidal activity. J Immunol 1987;139(4):1342–1347.
 
25. Wirth JJ, et al. FASEB Journal 1988;2(4):PA453.
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