The Influence of Antigen-Presenting Cell Type and Interferon- on Priming and Cytokine Secretion of Leishmania major--Specific T Cells
Author(s) -
Anuraj H. Shankar,
Richard G. Titus
Publication year - 1997
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1093/infdis/175.1.151
Subject(s) - priming (agriculture) , biology , leishmania major , secretion , cytokine , interleukin 12 , interferon , antigen presenting cell , immune system , cd40 , immunology , dendritic cell , leishmania , microbiology and biotechnology , t cell , in vitro , cytotoxic t cell , endocrinology , parasite hosting , biochemistry , botany , germination , world wide web , computer science
A Leishmania major-specific primary in vitro system that mimics the immune response of infected mice was used to determine the role that dendritic cells, B cells, and macrophages play in L. major T cell priming. Their relative priming potential (in order) was dendritic cells, B cells, and macrophages. Initiating primary in vitro responses with cell populations depleted of either B or dendritic cells modestly enhanced interferon (IFN)-gamma production; deleting both cells markedly enhanced IFN-gamma production. Thus, macrophages were the most effective cell for eliciting L. major Th1 cells. The effects of exogenously added IFN-gamma or neutralizing anti-IFN-gamma were also studied. With cells from genetically susceptible BALB/c mice, IFN-gamma inhibited proliferation and interleukin-4 secretion by T cells, whereas with resistant C57BL/6 cells, IFN-gamma enhanced IFN-gamma secretion. These results could not be explained by differences in IFN-gamma receptor expression.
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