Role of Bacterial Lipopolysaccharide in Enhancing Host Immune Response to <i>Candida albicans</i>

<table>Heat-killed <i>Candida-</i>(HKC-) induced IL-23 expression in human monocytes in cell cultures containing LPS. (a) LPS pretreated human PBMC with HKC challenge and expression of mRNA for IL-12p40 and IL-23p19 subunits of IL-23. A significantly increased IL-23 production in an LPS dose-dependent manner was evident compared to cells without LPS stimulation (<svg height="13.95" id="M15" style="vertical-align:-0.1638pt" version="1.1" viewbox="0 0 73.300003 13.95" width="73.300003" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
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</svg>). (b) Human monocytes cell line (THP-1) produced IL-23 in a dose-dependent manner in the cell cultures together with LPS. (c) Human PBMC produced IL-17A after days 1, 3, and 7 cultured with 3 different clinical strains of HKC.</table>

Journal of Immunology Research

fig3

Figure 3

Figure 3: Role of Bacterial Lipopolysaccharide in Enhancing Host Immune Response to <i>Candida albicans</i> 

Journal of Immunology Research

Role of Bacterial Lipopolysaccharide in Enhancing Host Immune Response to Candida albicans

Figure 3