In this study, we have attempted to determine whether the systemic administration of CpG oligodeoxynucleotide (CpG-ODN) 1826 would protect mice against systemic lethal Candida albicans infection. CpG-ODNs were found completely to protect mice from death and also reduced the growth of C. albicans in the kidneys. The administration of CpG-ODNs resulted in early interleukin (IL)-12 mRNA expression in the kidneys and an increase in serum IL-12 levels. The protective activity of CpG-ODN was abolished in IL-12-deficient (IL-12 -/-) mice, thereby indicating the IL-12-dependency inherent to the effects of CpG-ODN. The protective effect of CpG-ODN was not associated with the activity of NF-κB. Interestingly, in tumor necrosis factor (TNF)-α-deficient (TNF-/-) mice CpG-ODN neither exerted protective effects nor induced IL-12 expression. These data indicate that CpG-ODN protects animals against lethal C. albicans challenge via a pathway that involves the TNF-α-dependent induction of IL-12. © 2007 Federation of European Microbiological Societies.
CITATION STYLE
Choi, J. H., Ko, H. M., Park, S. J., Kim, K. J., Kim, S. H., & Im, S. Y. (2007). CpG oligodeoxynucleotides protect mice from lethal challenge with Candida albicans via a pathway involving tumor necrosis factor-α-dependent interleukin-12 induction. FEMS Immunology and Medical Microbiology, 51(1), 155–162. https://doi.org/10.1111/j.1574-695X.2007.00292.x
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