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
Production of interferon-γ and interleukin-4 by splenocytes in mice infected with Paragonimus westermani
| Home | E-Submission | Sitemap | Contact us |  
top_img
Korean J Parasito Search

CLOSE

Korean J Parasito > Volume 34(3):1996 > Article

Original Article
Korean J Parasitol. 1996 Sep;34(3):185-189. English.
Published online Sep 20, 1996.  http://dx.doi.org/10.3347/kjp.1996.34.3.185
Copyright © 1996 by The Korean Society for Parasitology
Production of interferon-γ and interleukin-4 by splenocytes in mice infected with Paragonimus westermani
M H Shin,*1 and D Y Min2
1Department of Parasitology, College of Medicine, Ewha Womans University, Seoul 158-056, Korea.
Received May 11, 1996; Accepted July 31, 1996.

Abstract

The TH cytokine responses of spleen cells stimulated with Con A from mice infected with Paragonimus westermani were examined. The spleen cell culture supernatants were assayed for TH1-specific IFN-γ and TH2-specific IL-4. Cytokine responses for IL-4 peaked at three days (410 ± 60.9 pg/ml), persisted at a high level until the second week (343 ± 59.0 pg/ml), and then decreased slowly four and six weeks after infection. IFN-γ production by splenocytes only increased during the first week (151 ± 32.3 pg/ml) and declined abruptly after the second week of infection. IFN-γ production by splenocytes of infected mice was not observed during the sixth week of infection. In addition, serum IL-4 and IFN-γ were measured. Serum IL-4 was not detected in substantial quantity until four to six weeks after infection. The time course of serum IL-4 was not correlated with that of IL-4 production by splenocytes. Serum IFN-γ was undetectable during the entire course of infection. These results suggest that TH2 cytokine responses, rather than TH1, predominate in mice infected with P. westermani.

Tables


Table 1
Cytokine levels (pg/ml) in splenocyte culture supernatant of mice infected with Paragonimus westermani


Table 2
Serum cytokine level (pg/ml) in mice infected with Paragonimus westermani

References
1. Amiri P, Haak-Frendscho M, Robbins K, McKerrow JH, Stewart T, Jardieu P. Anti-immunoglobulin E treatment decreases worm burden and egg production in Schistosoma mansoni-infected normal and interferon gamma knockout mice. J Exp Med 1994;180(1):43–51.
  
2. Coffman RL, Ohara J, Bond MW, Carty J, Zlotnik A, Paul WE. B cell stimulatory factor-1 enhances the IgE response of lipopolysaccharide-activated B cells. J Immunol 1986;136(12):4538–4541.
 
3. Else KJ, Finkelman FD, Maliszewski CR, Grencis RK. Cytokine-mediated regulation of chronic intestinal helminth infection. J Exp Med 1994;179(1):347–351.
  
4. Else KJ, Grencis RK. Helper T-cell subsets in mouse trichuriasis. Parasitol Today 1991;7(11):313–316.
  
5. Finkelman FD, Katona IM, Urban JF Jr, Snapper CM, Ohara J, Paul WE. Suppression of in vivo polyclonal IgE responses by monoclonal antibody to the lymphokine B-cell stimulatory factor 1. Proc Natl Acad Sci U S A 1986;83(24):9675–9678.
  
6. Grzych JM, Pearce E, Cheever A, Caulada ZA, Caspar P, Heiny S, Lewis F, Sher A. Egg deposition is the major stimulus for the production of Th2 cytokines in murine schistosomiasis mansoni. J Immunol 1991;146(4):1322–1327.
 
7. Habe S. Jpn J Parasitol 1978;27:261–292.
8. Min DY, Ryu JS, Shin MH. Changes of IgE production, splenic helper and suppressor T lymphocytes in mice infected with Paragonimus westermani. Korean J Parasitol 1993;31(3):231–238.
  
9. Mosmann TR, Cherwinski H, Bond MW, Giedlin MA, Coffman RL. Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins. J Immunol 1986;136(7):2348–2357.
 
10. Pond L, Wassom DL, Hayes CE. Evidence for differential induction of helper T cell subsets during Trichinella spiralis infection. J Immunol 1989;143(12):4232–4237.
 
11. Radermecker M, Bekhti A, Poncelet E, Salmon J. Serum IgE levels in protozoal and helminthic infections. Int Arch Allergy Appl Immunol 1974;47(2):285–295.
  
12. Ramaswamy K, Goodman RE, Bell RG. Cytokine profile of protective anti-Trichinella spiralis CD4+ OX22- and non-protective CD4+ OX22+ thoracic duct cells in rats: secretion of IL-4 alone does not determine protective capacity. Parasite Immunol 1994;16(8):435–445.
  
13. Sher A, Coffman RL, Hieny S, Cheever AW. Ablation of eosinophil and IgE responses with anti-IL-5 or anti-IL-4 antibodies fails to affect immunity against Schistosoma mansoni in the mouse. J Immunol 1990;145(11):3911–3916.
 
14. Silva JS, Morrissey PJ, Grabstein KH, Mohler KM, Anderson D, Reed SG. Interleukin 10 and interferon gamma regulation of experimental Trypanosoma cruzi infection. J Exp Med 1992;175(1):169–174.
  
15. Urban JF Jr, Katona IM, Paul WE, Finkelman FD. Interleukin 4 is important in protective immunity to a gastrointestinal nematode infection in mice. Proc Natl Acad Sci U S A 1991;88(13):5513–5517.
  
16. Urban JF Jr, Madden KB, Cheever AW, Trotta PP, Katona IM, Finkelman FD. IFN inhibits inflammatory responses and protective immunity in mice infected with the nematode parasite, Nippostrongylus brasiliensis. J Immunol 1993;151(12):7086–7094.
 
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