Abstract
Gamma interferon (IFN-gamma) previously has been shown to block the replication of Toxoplasma gondii in fibroblasts by the induction of indoleamine 2,3-dioxygenase (IDO) activity. IFN-beta also is known to induce IDO activity in monocyte-derived macrophages, but its ability to block the growth of T. gondii has not been demonstrated. We found not only that the combination of IFN-beta and lipopolysaccharide induced greater IDO activity in monocyte-derived macrophages than did IFN-beta alone but that this combination also was effective in inhibiting the growth of T. gondii. In addition, the inhibition was reversed by the addition of exogenous tryptophan, thus demonstrating that a mechanism by which IFN-beta inhibited T. gondii replication was by the induction of IDO.
MeSH Terms
Animals
Enzyme Activation/drug effects
Growth Inhibitors/pharmacology
Humans
Indoleamine-Pyrrole 2,3,-Dioxygenase
Interferon Type I/pharmacology
Interferon-gamma/pharmacology
Lipopolysaccharides/pharmacology
Macrophages/drug effects,enzymology,parasitology
Monocytes/drug effects,enzymology,parasitology
Oxygenases/metabolism,physiology
Toxoplasma/drug effects,growth & development
Tryptophan Oxygenase
Chemicals
Growth Inhibitors
Indoleamine-Pyrrole 2,3,-Dioxygenase
Interferon Type I
Lipopolysaccharides
Interferon-gamma
Oxygenases
Tryptophan Oxygenase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Schmitz J L
Department of Medical Microbiology and Immunology, University of Wisconsin Medical School, Madison 53706.
Carlin J M
Borden E C
Byrne G I
References (13)
13 references, click to expand
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