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    Interferon-g mediated immune effector mechanisms against Bordetella pertussis

    Mahon, Bernard P. and Mills, Kingston H.G. (1999) Interferon-g mediated immune effector mechanisms against Bordetella pertussis. Immunology Letters, 68. pp. 213-217.

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    The role of IFN-g in reducing the intracellular load of Bordetella pertussis in murine macrophages in vitro has been examined. The results demonstrate that exposure to IFN-g can reduce bacterial load in viable macrophages and that this is associated with production of nitric oxide (NO). These observations provide a mechanism by which IFN-g may mediate its antimicrobial effect and support an important role for activated alveolar macrophages in the elimination of B. pertussis from the respiratory tract. Using intracellular iron chelation, it is shown that intracellular survival of B. pertussis is dependant on iron availability and suggest that iron restriction may be an important mechanism by which IFN-g influences bacterial survival within mouse macrophages. It is also shown that IFN-g may mediate its effect through NO independent mechanisms and that B. pertussis is sensitive to agents that stimulate the respiratory burst. Finally, it is shown that the concentration of L-tryptophan may be a limiting step in the intracellular survival of B. pertussis and that the induction of tryptophan degrading enzymes may be an additional mechanism through which IFN-g exerts its antimicrobial effects against B. pertussis.

    Item Type: Article
    Keywords: Pertussis; Interferon-g; Nitric oxide; Iron; Indoleamine 2,3-dioxygenase;
    Academic Unit: Faculty of Science and Engineering > Biology
    Faculty of Science and Engineering > Research Institutes > Institute of Immunology
    Item ID: 169
    Depositing User: Bernard Mahon
    Date Deposited: 04 Jan 2005
    Journal or Publication Title: Immunology Letters
    Publisher: Elsevier Science B.V.
    Refereed: Yes
      Use Licence: This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA). Details of this licence are available here

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