Recombinant Interleukin‐18 Protects against DisseminatedCandida albicansInfection in Mice
Author(s) -
Rogier J. L. Stuyt,
Mihai G. Netea,
J. Han van Krieken,
Jos W.M. van der Meer,
Bart Jan Kullberg
Publication year - 2004
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 - 10.1086/382955
Subject(s) - candida albicans , splenocyte , immunotherapy , corpus albicans , adjuvant , recombinant dna , immunology , interleukin 2 , cytokine , biology , microbiology and biotechnology , endogeny , systemic candidiasis , inflammation , interleukin , interferon gamma , medicine , spleen , immune system , endocrinology , biochemistry , gene
Endogenous interleukin (IL)-18 is necessary for host defense against candidiasis. Prophylactic treatment of Candida albicans-infected mice with recombinant murine (r) IL-18 decreased mortality, which was accompanied by a decreased outgrowth of yeasts in the kidneys 1 day after infection. Therapeutic administration of rIL-18 also resulted in decreased outgrowth of C. albicans in the kidneys and increased levels of interferon- gamma, both in the circulation and after in vitro stimulation of splenocytes with C. albicans. Histopathologic analysis of the kidneys showed increased inflammation and decreased growth of C. albicans in rIL-18-treated mice. In conclusion, rIL-18 improves outcome of disseminated candidiasis in mice and may prove useful as adjuvant immunotherapy of fungal infections.
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