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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

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