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

Warning: fopen(upload/ip_log/ip_log_2024-04.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
Interleukin-2 production and alteration of T cell subsets in mice infected with Naegleria fowleri
| Home | E-Submission | Sitemap | Contact us |  
top_img
Korean J Parasito Search

CLOSE

Korean J Parasito > Volume 31(3):1993 > Article

Original Article
Korean J Parasitol. 1993 Sep;31(3):249-257. English.
Published online Mar 20, 1994.  http://dx.doi.org/10.3347/kjp.1993.31.3.249
Copyright © 1993 by The Korean Society for Parasitology
Interleukin-2 production and alteration of T cell subsets in mice infected with Naegleria fowleri
C J Lyu,C O Shin and K Im*
Department of Parasitology & Institute of Tropical Medicine, College of Medicine, Yonsei University, Seoul 120-752, Korea.
Received July 02, 1993; Accepted July 31, 1993.

Abstract

Naegleria fowleri is the cause of primary amoebic meningoencephalitis in man. IL-2 levels after stimulation of T lymphocytes by PHA or N. fowleri lysates, the amounts of T lymphocyte subsets and the blastogenic responses of T lymphocytes in mice after infected with pathogenic N. fowleri were studied comparing between two study groups, one 1 × 104 trophozoites inoculated mice and the other 1 × 105 trophozoites inoculated mice. All experimental samples were obtained on the day 7, 14 and 24 after inoculation. The mice inoculated with 1 × 104 trophozoites showed a 14.3% mortality rate, and 72.2% in the mice inoculated with 1 × 105 trophozoites. The IL-2 levels on day 14 of two experimental groups were significantly decreased as compared with the control group. Thy 1.2+ T cells in the total spleen lymphocytes of 1 × 105 trophozoites inoculated group on day 7 were significantly increased compared with the control group. There was no significant difference between 1 × 104 trophozoites inoculated group and the control group. L3T4+ T cells and Ly2+ T cells in the total spleen lymphocytes of 1 × 105 trophozoites inoculated group on day 7 were significantly increased compared with the control group. The DNA S fraction of T cells in the spleen of 1 × 105 trophozoites inoculated group was significantly increased on day 7. The amount of S fractions of DNA were sequentially decreased on day 14 and 24, but they were also significantly increased compared with the control group.(ABSTRACT TRUNCATED AT 250 WORDS)

Figures


Fig. 1
Mortality of mice inoculated with N. fowleri trophozoites.


Fig. 2
The ratio of Thy 1,2+ T cells to spleen lymphocytes in mice inoculated with N. fowleri trophozoites.


Fig. 3
The ratio of L3T4+ T cells to spleen lymphocytes in mice inoculated with N. fowleri trophozoites.


Fig. 4
The ratio of Ly2+ T cells to spleen lymphocytes in mice inoculated with N. fowleri trophozoites.


Fig. 5
The ratio of L3T4+ T/Ly2+ T cells to spleen lymphocytes in mice inoculated with N. fowleri trophozoites.

Tables


Table 1
IL-2 production of spleen cells treated with PHA, N. fowleri lysates in mice inoculated with N. fowleri trophozoites


Table 2
S phase fraction of splenic T cells in mice inoculated with N. fowleri trophozoites

References
1. Kim KH, Shin CO, Im K. [Natural killer cell activity in mice infected with free-living amoeba with reference to their pathogenicity]. Korean J Parasitol 1993;31(3):239–248.
  
2. Kim MJ, Shin CO, Im KI. [Cell-mediated immunity in mice infected with Acanthamoeba culbertsoni]. Korean J Parasitol 1990;28(3):143–154.
 
3. Park KM, Ryu JS, Im KI. [Blastogenic responses of splenic lymphocytes to Naegleria fowleri lysates and T-cell mitogen in mice with primary amoebic meningoencephalitis]. Korean J Parasitol 1987;25(1):1–6.
 
4. Lee KR, Shin CO, Im K. [Natural killer cell activity in Naegleria fowleri infected mice]. Korean J Parasitol 1991;29(3):267–277.
 
6. Britten V, et al. Trop Med Parasit 1986;37:97–100.
7. Carter RF. J Porth Bacteriol 1986;96:1–25.
 
8. Cursons RT, Brown TJ, Keys EA, Moriarty KM, Till D. Immunity to pathogenic free-living amoebae: role of cell-mediated immunity. Infect Immun 1980;29(2):408–410.
 
9. Diamantstein T, Klos M, Gold D, Hahn H. Interaction between Entamoeba histolytica and the immune system. I. Mitogenicity of Entamoeba histolytica extracts for human peripheral T lymphocytes. J Immunol 1981;126(6):2084–2086.
 
10. Farrar JJ, Benjamin WR, Hilfiker ML, Howard M, Farrar WL, Fuller-Farrar J. The biochemistry, biology, and role of interleukin 2 in the induction of cytotoxic T cell and antibody-forming B cell responses. Immunol Rev 1982;63:129–166.
  
11. Ferrante A. Free-living amoebae: pathogenicity and immunity. Parasite Immunol 1991;13(1):31–47.
  
12. Ferrante A, Smyth C. Mitogenicity of Naegleria fowleri extract for murine T lymphocytes. Immunology 1984;51(3):461–468.
 
13. Ferrante A, Thong YH. Antibody induced capping and endocytosis of surface antigens in Naegleria fowleri. Int J Parasitol 1979;9(6):599–601.
  
14. Gillis S, Ferm MM, Ou W, Smith KA. T cell growth factor: parameters of production and a quantitative microassay for activity. J Immunol 1978;120(6):2027–2032.
 
15. Hay J, Dutton GN, Hair DM. Blastogenic responses of splenic lymphocytes to toxoplasmal and retinal antigens and T- and B-cell mitogens in mice with congenital ocular toxoplasmosis. Ann Trop Med Parasitol 1985;79(1):113–115.
 
16. Kierszenbaum F. Immunologic deficiency during experimental Chagas' disease (Trypanosoma cruzi infection): role of adherent, nonspecific esterase-positive splenic cells. J Immunol 1982;129(5):2202–2205.
 
17. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951;193(1):265–275.
 
18. Martinez J, Duma RJ, Nelson EC, Moretta FL. Experimental naegleria meningoencephalitis in mice. Penetration of the olfactory mucosal epithelium by Naegleria and pathologic changes produced: a light and electron microscope study. Lab Invest 1973;29(2):121–133.
 
19. Morgan DA, Ruscetti FW, Gallo R. Selective in vitro growth of T lymphocytes from normal human bone marrows. Science 1976;193(4257):1007–1008.
  
21. Reed SG, Inverso JA, Roters SB. Heterologous antibody responses in mice with chronic T. cruzi infection: depressed T helper function restored with supernatants containing interleukin 2. J Immunol 1984;133(3):1558–1563.
 
22. Rowan-Kelly B, Ferrante A, Thong YH. Activation of complement by Naegleria. Trans R Soc Trop Med Hyg 1980;74(3):333–336.
  
23. Schurr E, Kidane K, Yemaneberhan T, Wunderlich F. Cutaneous leishmaniasis in Ethiopia: I. Lymphocyte transformation and antibody titre. Trop Med Parasitol 1986;37(4):403–408.
 
25. Selkirk ME, Ogilvie BM, Platts-Mills TA. Activation of human peripheral blood lymphocytes by a trypanosome-derived mitogen. Clin Exp Immunol 1981;45(3):615–620.
 
26. Suzuki Y, Kobayashi A. Macrophage-mediated suppression of immune responses in Toxoplasma-infected mice. I. Inhibition of proliferation of lymphocytes in primary antibody responses. Cell Immunol 1984;85(2):417–427.
  
27. Svedersky LP, Shepard HM, Spencer SA, Shalaby MR, Palladino MA. Augmentation of human natural cell-mediated cytotoxicity by recombinant human interleukin 2. J Immunol 1984;133(2):714–718.
 
28. Tarleton RL. Regulation of immunity in Trypanosoma cruzi infection. Exp Parasitol 1991;73(1):106–109.
  
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