Rouabhia Mahmoud, Ross Geneviève, Pagé Nathalie, Chakir Jamila
Faculté de médecine dentaire. GREB, Université Laval, Québec G1K 7P4, Canada.
Infect Immun. 2002 Dec;70(12):7073-80. doi: 10.1128/IAI.70.12.7073-7080.2002.
Oral candidiasis is a collective name for a group of disorders caused by the dimorphic fungus Candida albicans. Host defenses against C. albicans essentially fall into two categories: specific immune mechanisms and local oral mucosal epithelial cell defenses. Since oral epithelial cells secrete a variety of cytokines and chemokines in response to oral microorganisms and since C. albicans is closely associated with oral epithelial cells as a commensal organism, we wanted to determine whether interleukin-18 (IL-18) and gamma interferon (IFN-gamma) were produced by oral epithelial cells in response to C. albicans infection and lipopolysaccharide (LPS) stimulation. Our results showed that IL-18 mRNA and protein were constitutively expressed by oral epithelial cells and were down-regulated by Candida infections but increased following LPS stimulation. Both C. albicans and LPS significantly decreased pro-IL-18 (24 kDa) levels and increased active IL-18 (18 kDa) levels. This effect was IL-1beta-converting-enzyme dependent. The increase in active IL-18 protein levels promoted the production of IFN-gamma by infected cells. No effect was obtained with LPS. Although produced only at an early stage, secreted IFN-gamma seemed to be a preferential response by oral epithelial cells to C. albicans growth. These results provide additional evidence for the contribution of oral epithelial cells to local (direct contact) and systemic (IL-18 and IFN-gamma production) defense against exogenous stimulation such as C. albicans infection or LPS stimulation.
口腔念珠菌病是由二态真菌白色念珠菌引起的一组病症的统称。宿主针对白色念珠菌的防御机制主要分为两类:特异性免疫机制和口腔局部黏膜上皮细胞防御机制。由于口腔上皮细胞会针对口腔微生物分泌多种细胞因子和趋化因子,并且白色念珠菌作为共生菌与口腔上皮细胞密切相关,因此我们想确定白细胞介素-18(IL-18)和γ干扰素(IFN-γ)是否由口腔上皮细胞在白色念珠菌感染和脂多糖(LPS)刺激下产生。我们的结果表明,IL-18 mRNA和蛋白在口腔上皮细胞中组成性表达,在念珠菌感染时下调,但在LPS刺激后增加。白色念珠菌和LPS均显著降低前体IL-18(24 kDa)水平并增加活性IL-18(18 kDa)水平。这种效应依赖于IL-1β转换酶。活性IL-18蛋白水平的增加促进了感染细胞产生IFN-γ。LPS对此没有影响。尽管IFN-γ仅在早期产生,但分泌的IFN-γ似乎是口腔上皮细胞对白色念珠菌生长的优先反应。这些结果为口腔上皮细胞在针对白色念珠菌感染或LPS刺激等外源性刺激的局部(直接接触)和全身(产生IL-18和IFN-γ)防御中的作用提供了额外证据。