Department of Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia B3H 1X5, Canada.
J Virol. 2011 Jan;85(2):1145-50. doi: 10.1128/JVI.01630-10. Epub 2010 Nov 10.
Vascular perturbation is a hallmark of severe forms of dengue disease. We show here that antibody-enhanced dengue virus infection of primary human cord blood-derived mast cells (CBMCs) and the human mast cell-like line HMC-1 results in the release of factor(s) which activate human endothelial cells, as evidenced by increased expression of the adhesion molecules ICAM-1 and VCAM-1. Endothelial cell activation was prevented by pretreatment of mast cell-derived supernatants with a tumor necrosis factor (TNF)-specific blocking antibody, thus identifying TNF as the endothelial cell-activating factor. Our findings suggest that mast cells may represent an important source of TNF, promoting vascular endothelial perturbation following antibody-enhanced dengue virus infection.
血管功能紊乱是登革热严重病症的一个显著特征。我们在这里表明,通过原发性人脐血衍生的肥大细胞(CBMC)和人肥大细胞样系 HMC-1 增强的抗体增强登革病毒感染会导致释放激活人内皮细胞的因子,这一点可以通过细胞间黏附分子 1(ICAM-1)和血管细胞黏附分子 1(VCAM-1)的表达增加得到证明。肥大细胞来源的上清液预先用肿瘤坏死因子(TNF)特异性阻断抗体处理,可以防止内皮细胞的激活,因此鉴定 TNF 为内皮细胞激活因子。我们的研究结果表明,肥大细胞可能是 TNF 的一个重要来源,促进了抗体增强登革病毒感染后的血管内皮功能紊乱。