Sittisombut N, Maneekarn N, Kanjanahaluethai A, Kasinrerk W, Viputtikul K, Supawadee J
Department of Microbiology, Faculty of Medicine, Chiang Mai University, Thailand.
J Med Virol. 1995 Jan;45(1):43-9. doi: 10.1002/jmv.1890450109.
The effect of interferon-gamma (IFN-gamma) on dengue virus multiplication in human peripheral blood monocytes was investigated. Enriched monocytes were treated with IFN-gamma and then infected with dengue virus type 2 either directly or in the presence of optimal infection-enhancing levels of antibodies. Pretreatment of monocytes from dengue-immune donors with 100 IU/ml of IFN-gamma caused 12- to 97-fold and 13- to 137-fold reduction of virus yields at 24 hr after infection in the absence and presence of an anti-flavivirus monoclonal antibody, respectively. IFN-gamma also diminished virus yields when infection of monocytes from a donor who lacked anti-dengue antibody was enhanced 40-fold. The percentage of infected monocytes in IFN-gamma-pretreated cultures was similarly reduced. Dominance of the antiviral effect of IFN-gamma in monocytes is in contrast to an augmenting effect previously observed in the promonocytic cell line U937.
研究了γ干扰素(IFN-γ)对登革病毒在人外周血单核细胞中增殖的影响。用IFN-γ处理富集的单核细胞,然后直接或在存在最佳感染增强水平抗体的情况下用2型登革病毒感染。用100 IU/ml的IFN-γ预处理来自登革热免疫供体的单核细胞,在不存在和存在抗黄病毒单克隆抗体的情况下,感染后24小时病毒产量分别降低12至97倍和13至137倍。当缺乏抗登革热抗体的供体的单核细胞感染增强40倍时,IFN-γ也降低了病毒产量。IFN-γ预处理培养物中被感染单核细胞的百分比也同样降低。IFN-γ在单核细胞中的抗病毒作用占主导地位,这与先前在原单核细胞系U937中观察到的增强作用形成对比。