Gulraiz Fahad, Bellinghausen Carla, Dentener Mieke A, Reynaert Niki L, Gaajetaan Giel R, Beuken Erik V, Rohde Gernot G, Bruggeman Cathrien A, Stassen Frank R
Department of Medical Microbiology, Maastricht University Medical Centre, Maastricht, the Netherlands.
Department of Medical Microbiology, Maastricht University Medical Centre, Maastricht, the Netherlands; Department of Respiratory Medicine, Maastricht University Medical Centre, Maastricht, the Netherlands.
PLoS One. 2014 Apr 21;9(4):e95134. doi: 10.1371/journal.pone.0095134. eCollection 2014.
Impaired interferon (IFN) production has been observed in various obstructive respiratory diseases. This contributes to enhanced sensitivity towards viral infections triggering acute exacerbations. To compensate for this impaired host IFN response, there is need to explore new therapeutic strategies, like exogenous administration of IFNs as prophylactic treatment. In the present study, we examined the protective potential of IFN-λ1 and compared it with the previously established protecting effect of IFN-β. A549 cells and human primary bronchial epithelial cells were first treated with either IFN-β (500 IU/ml) or IFN-λ1 (500 ng/ml) for 18 h. For infection, two approaches were adopted: i) Continuous scenario: after pre-treatment, cells were infected immediately for 24 h with human rhinovirus 1B (HRV1B) in IFN-containing medium, or were cultured for another 72 h in IFN-containing medium, and then infected for 24 h with HRV1B, ii) Pre-treatment scenario: IFN-containing medium was replaced after 18 h and cells were infected for 4 h either immediately after pre-treatment or after additional culturing for 72 h in IFN-free medium. The protective effect was evaluated in terms of reduction in the number of viral copies/infectious progeny, and enhanced expression of IFN-stimulated genes (ISGs). In both cell types and in both approaches, IFN-λ1 and IFN-β treatment resulted in pronounced and long-lasting antiviral effects exemplified by significantly reduced viral copy numbers and diminished infectious progeny. This was associated with strong up-regulation of multiple ISGs. However, in contrast to the IFN-β induced expression of ISGs, which decreased over time, expression of ISGs induced by IFN-λ1 was sustained or even increased over time. Here we demonstrate that the protective potential of IFN-λ1 is comparable to IFN-β. Yet, the long-lasting induction of ISGs by IFN-λ1 and most likely less incitement of side effects due to more localized expression of its receptors could make it an even more promising candidate for prophylactic treatment than IFN-β.
在各种阻塞性呼吸道疾病中均观察到干扰素(IFN)产生受损。这导致对引发急性加重的病毒感染的敏感性增强。为了弥补这种受损的宿主IFN反应,需要探索新的治疗策略,如作为预防性治疗进行外源性IFN给药。在本研究中,我们检测了IFN-λ1的保护潜力,并将其与先前确立的IFN-β的保护作用进行比较。首先用IFN-β(500 IU/ml)或IFN-λ1(500 ng/ml)处理A549细胞和人原代支气管上皮细胞18小时。对于感染,采用了两种方法:i)连续情况:预处理后,细胞立即在含IFN的培养基中用人鼻病毒1B(HRV1B)感染24小时,或在含IFN的培养基中再培养72小时,然后用HRV1B感染24小时,ii)预处理情况:18小时后更换含IFN的培养基,细胞在预处理后立即或在无IFN培养基中再培养72小时后感染4小时。根据病毒拷贝数/感染后代数量的减少以及IFN刺激基因(ISG)表达的增强来评估保护作用。在两种细胞类型和两种方法中,IFN-λ1和IFN-β处理均产生了显著且持久的抗病毒作用,表现为病毒拷贝数显著减少和感染后代减少。这与多种ISG的强烈上调相关。然而,与IFN-β诱导的ISG表达随时间下降不同,IFN-λ1诱导的ISG表达随时间持续甚至增加。我们在此证明,IFN-λ1的保护潜力与IFN-β相当。然而,IFN-λ1对ISG的持久诱导以及由于其受体更局限的表达而最有可能较少引发副作用,这可能使其成为比IFN-β更有前景的预防性治疗候选药物。