Warning: mkdir(): Permission denied in /home/virtual/lib/view_data.php on line 81

Warning: fopen(upload/ip_log/ip_log_2024-11.txt): failed to open stream: No such file or directory in /home/virtual/lib/view_data.php on line 83

Warning: fwrite() expects parameter 1 to be resource, boolean given in /home/virtual/lib/view_data.php on line 84
Cytotoxicity of resident and lymphokine-activated mouse peritoneal macrophage against Trichomonas vaginalis
| Home | E-Submission | Sitemap | Contact us |  
top_img
Korean J Parasito Search

CLOSE

Korean J Parasito > Volume 28(2):1990 > Article

Original Article
Korean J Parasitol. 1990 Jun;28(2):85-89. English.
Published online Mar 20, 1994.  http://dx.doi.org/10.3347/kjp.1990.28.2.85
Copyright © 1990 by The Korean Society for Parasitology
Cytotoxicity of resident and lymphokine-activated mouse peritoneal macrophage against Trichomonas vaginalis
J S Ryu,M H Ahn and D Y Min
Department of Parasitology, College of Medicine, Hanyang University, Seoul 133-791, Korea.
Abstract

This study was aimed to observe the direct and lymphokine-activated cell mediated cytotoxic effects against Trichomonas vaginalis by mouse peritoneal macrophages. Cytotoxicity was measured as release of 3H-thymidine from prelabeled protozoa, and tested in U-bottom microtiter plates. A 0.1 ml suspension of labeled protozoa (2 × 105/ml) was placed in each well, followed by 0.1 ml of a suspension containing increasing numbers of peritoneal cells. After a 24 hr incubation at 37℃, 0.1 ml of the supernatant was collected and counted in liquid scintillation counter.

Mouse peritoneal macrophages had appreciable level of spontaneous cytotoxicity against T. vaginalis at the effector to target cell ratios from 5:1 to 50:1. Treatment of macrophages with lymphokine, produced by PHA-stimulated spleen cells, increased the cytotoxicity in comparison with resident macrophages against T. vaginalis. The degree of macrophage activation for the killing was not dependent upon the lymphokine concentration. Peritoneal cells adherent to plastic displayed significant levels of cytotoxicity against T. vaginalis.

This study indicates that mouse peritoneal macrophages are spontaneously cytotoxic for T. vaginalis and lymphokine increases the cytotoxicity by activating macrophages to kill T. vaginalis.

Tables


Table 1
Cytotoxicity of mouse macrophages against T. vaginalis in different E : T ratios and incubation times


Table 2
Cytotoxicity of peritoneal cells against T. vaginalis


Table 3
Cytotoxicity of lymphokine-activated macrophages from normal & immunized mice against T. vaginalis


Table 4
Effect of lymphokine concentrations on the macrophage cytotoxicity against T. vaginalis

References
1. Belosevic M, Faubert GM. Killing of Giardia muris trophozoites in vitro by spleen, mesenteric lymph node and peritoneal cells from susceptible and resistant mice. Immunology 1986;59(2):269–275.
 
2. Bout DT, et al. J Immunol 1981;27(1):1–5.
3. Diamond LS. Techniques of axenic cultivation of Entamoeba histolytica Schaudinn, 1903 and E. histolytica-like amebae. J Parasitol 1968;54(5):1047–1056.
  
4. Freund M, Pick E. The mechanism of action of lymphokines. VIII. Lymphokine-enhanced spontaneous hydrogen peroxide production by macrophages. Immunology 1985;54(1):35–45.
 
5. 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.
 
6. Kanwar SS, Walia BN, Ganguly NK, Mahajan RC. The macrophages as an effector cell in Giardia lamblia infections. Med Microbiol Immunol 1987;176(2):83–88.
  
7. 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.
 
8. 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.
 
9. 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.
  
10. Passwell JH, Shor R, Gazit E, Shoham J. The effects of Con A-induced lymphokines from the T-lymphocyte subpopulations on human monocyte leishmanicidal capacity and H2O2 production. Immunology 1986;59(2):245–250.
 
11. Reed SG, Douglass TG, Speer CA. Surface interactions between macrophages and Trypanosoma cruzi. Am J Trop Med Hyg 1982;31(4):723–729.
 
12. Smith PD, Elson CO, Keister DB, Nash TE. Human host response to Giardia lamblia. I. Spontaneous killing by mononuclear leukocytes in vitro. J Immunol 1982;128(3):1372–1376.
 
Editorial Office
Department of Molecular Parasitology, Samsung Medical Center, School of Medicine, Sungkyunkwan University,
2066 Seobu-ro, Jangan-gu, Suwon 16419, Gyeonggi-do, Korea.
Tel: +82-31-299-6251   FAX: +82-1-299-6269   E-mail: kjp.editor@gmail.com
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
Copyright © 2024 by The Korean Society for Parasitology and Tropical Medicine.     Developed in M2PI