Author/Authors :
M. Barral-Netto، نويسنده , , R.L. Von Sohsten، نويسنده , , M. Teixeira، نويسنده , , W.L. Conrado dos Santos، نويسنده , , M.L. Pompeu، نويسنده , , R.A. Moreira، نويسنده , , J.T.A. Oliveira، نويسنده , , B.S. Cavada، نويسنده , , E. Falcoff، نويسنده , , A. Barral، نويسنده ,
Abstract :
In vivo administration of Canavalia brasiliensis lectin (at the time of infection, or maintained throughout the infection) reduced the lesions of highly susceptible BALB/c mice infected by Leishmania amazonensis. At the doses used C. brasiliensis lectin (ConBr) does not interfere with penetration or fate of Leishmania in the macrophages in vitro. Since Interferon-γ (IFN-γ) is the major macrophage activating factor, and considered a critical element in the successful immune response against leishmaniasis, we explored its participation in this phenomenon. ConBr either in vivo or in vitro induced IFN-γ production in normal or in leishmania-infected BALB/c mice. However we were unable to change the course of disease by in vivo IFN-γ administration (although IFN-γ preparations were effective in inducing a leishmanicidal effect in vitro on L. amazonensis-infected peritoneal macrophages). Additionally, IFN-γ neutralization with anti-IFN-γ monoclonal antibody did not alter the protection conferred by ConBr administration. These data show that lectin administration in vivo is protective in the otherwise unchecked L. amazonensis infection of BALB/c mice, and suggest that such effect is not mediated by IFN-γ.
Keywords :
Chagasי disease , Trypanosoma cruzi , Antigens , Humoral immunity , Lytic antibodies