CIBICI   14215
CENTRO DE INVESTIGACION EN BIOQUIMICA CLINICA E INMUNOLOGIA
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Epithelial cells of female genital tract mount a Type I Interferon response against Candida albicans
Autor/es:
RODRIGUEZ EMILSE; ICELY PA; CAEIRO JP; MIRÓ MS; MACCIONI M; SOTOMAYOR CE; VIGEZZI C; RIERA F
Lugar:
Curitiba
Reunión:
Congreso; Xv Forum on fungal infection in the Clinical Practice INFOCUS 2017; 2017
Institución organizadora:
INFOCUS
Resumen:
Introduction: Type I interferons (IFNs-I) constitute a family of pleiotropic cytokinesthat play a crucial role during infection by coordinating the function of different immunocompetent cells involved in the induction of defense against viruses and intracellular bacteria. However, recent studies have revealed that IFNs-I can also be producedin response to fungal pathogens, but their roles in antifungal immunity have not been thoroughly investigated. Candida albicans(Ca)is the most common human fungal pathogen causing both mucosal and systemic infections. Vulvovaginal candidiasis(VVC)is an acute inflammatory disease that affects 75% of women in reproductive age at least once in their lives. Nowadays, little is known about the ability of C.albicans to induce IFNs-I in female genital tract cells and the role of these cytokines during VVC.Objective: We aimed to study whether C.albicansrecognition can activate IFNs-I pathway in epithelial cells of female genital tract in order to establish a possible role during VVC. Methods:Human cervical epithelial cell line(HeLa) was stimulated withC.albicansSC5314 strainin three different conditions:Viable Infective(Ca)(fungus:cell ratio 0.25:1,0.5:1,1:1,5:1), viable Capseudomicelio(Amphotericin B-treated)(Capseudom)(5:1) andCaDNA(complexed with polyethylenimine)(CaDNA),during 4 and 24h. LPS and Poly I:C were used as activation controls. The expression of type IFNs-I pathway genes(IFN, IRF3, IRF7 and Mx1)was measured by qPCR and cytokine profile(IL1, IL6, TNF and TGF) by ELISA.Unstimulated cells were used as control.Results: We first evaluated the capacity ofHeLa cells to express IFNB mRNA in response to different stimuli. As expected, Poly I:C was able to induce a strong IFNB mRNA expression at 24h, while LPSshowed a significant increase at 4h(p