Hober D, Shen L, Benyoucef S, De Groote D, Deubel V, Wattré P
Laboratoire de Virologie, Bât IRFPPS, CHU, Lille, France.
Immunol Lett. 1996 Nov;53(2-3):115-20. doi: 10.1016/s0165-2478(96)02620-x.
The studies indicating the importance of TNF alpha in dengue virus infection have led us to determine whether monocyte-like cells produce TNF alpha exposure after dengue virus. The supernatant fluids of mosquito cells (AP61) infected with dengue virus (DV) type 1 and DV type 3 were harvested 7 days post-infection and clarified. DV inactivation was performed in the presence of betapropiolactone that preserves antigenicity of viruses. We used the monocytic-like cell line THP-1 that is a model system of TNF alpha production. Polymyxin B (50 micrograms/ml) was added to block untoward effects resulting from possible LPS contamination of media or cultures. THP-1 cells were primed with a phorbol ester (PMA) for 24 h, then they were cultured for 4 and 24 h in the presence of inactivated culture supernatant of dengue infected AP61 cells or control preparations. The concentrations of TNF alpha in the culture supernatants were measured by using an immunoenzymatic assay. PMA-treated THP-1 cells rapidly secreted TNF alpha in response to inactivated culture supernatant of DV-infected cells. We found high levels of TNF alpha with cells exposed to DV1 and DV3 preparations compared with controls (mean values; 465 and 829 vs. 70 pg/ml, respectively, at 24 h post exposure, n = 4). We obtained a substantial inhibition of the enhancing activity of DV1 and DV3 infected supernatants in the presence of dengue hyperimmune mouse ascitic fluids. Our results demonstrate that exposure of monocytes/macrophages to DV particles or virus proteins derived from DV may be responsible for the enhanced production of TNF alpha in DV-infected patients.
多项研究表明肿瘤坏死因子α(TNFα)在登革病毒感染中具有重要作用,这促使我们去确定单核细胞样细胞在接触登革病毒后是否会产生TNFα。在感染登革病毒1型(DV1)和登革病毒3型(DV3)的7天后,收集蚊细胞(AP61)的上清液并进行澄清处理。在β-丙内酯存在的情况下进行登革病毒灭活,以保留病毒的抗原性。我们使用单核细胞样细胞系THP-1,它是TNFα产生的模型系统。加入多粘菌素B(50微克/毫升)以阻断培养基或培养物中可能存在的脂多糖污染所产生的不良影响。用佛波酯(PMA)预处理THP-1细胞24小时,然后在登革病毒感染的AP61细胞的灭活培养上清液或对照制剂存在的情况下培养4小时和24小时。通过免疫酶测定法测量培养上清液中TNFα的浓度。PMA处理的THP-1细胞对登革病毒感染细胞的灭活培养上清液迅速分泌TNFα。我们发现,与对照组相比,接触DV1和DV3制剂的细胞中TNFα水平较高(暴露后24小时的平均值分别为465和829 vs. 70皮克/毫升,n = 4)。在登革热超免疫小鼠腹水存在的情况下,我们对DV1和DV3感染上清液的增强活性获得了显著抑制。我们的结果表明,单核细胞/巨噬细胞接触DV颗粒或源自DV的病毒蛋白可能是登革病毒感染患者中TNFα产生增加的原因。