Role of cytokines, NO, and H2O2 on the immunopathology of leptospirosis in genetically selected mice
J. venom. anim. toxins incl. trop. dis
;
11(2): 198-212, May-Aug. 2005. tab, graf
Article
in English
| LILACS
| ID: lil-402364
RESUMO
Immune response to leptospirosis is mainly humorally mediated, and involves opsonization of leptospires for phagocytosis by macrophages and neutrophils. However, some aspects are still unknown. For a more detailed analysis of the cellular immune response to leptospirosis infection, trials were carried out in order to determine the hydrogen peroxide and nitric oxide (H2O2 and NO)production stimulated or not by Interferon-gamma. The participation of some specific cytokines, such as Tumor Necrosis Factor-alfa (TNF-alfa); Interferon-gamma (IFN-y); Interleukin-6 (IL-6); and Interleukin-4 (IL-4), in the immunopathology of this infection was also investigated. For this purpose, we analyzed the supernatant from peritonealmacrophage cell culture and the splenic cells of mice genetically selected as High (H) and Low (L) antibody producers, and inbred Balb/c mice infected with Leptospira interrogans serovar icterohaemorrhagiae. The IL-6 production varied from release speaks to inhibition in H, L, and Balb/c mice. The three strains presented constant and elevated production of TNF-alfa until day 14, suggesting its effective participation in the initial phase of the infection. Meanwhile, all the three strains presented a constant and irregular IFN-y production, with release peaks between the 7th and 14th days in L mice. The H and Balb/c mice strains presented a higher tendency to Th2 response pattern, whereas L mice tendend towards Th1 response
Full text:
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Index:
LILACS (Americas)
Main subject:
Cytokines
/
Immunity, Cellular
/
Leptospirosis
/
Mice
Limits:
Animals
Language:
English
Journal:
J. venom. anim. toxins incl. trop. dis
Journal subject:
Toxicology
Year:
2005
Type:
Article
Affiliation country:
Brazil
Institution/Affiliation country:
São Paulo State Univeristy/BR
/
São Paulo State University/BR
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