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Lambda Interferon (IFN-λ), a Type III IFN, Is Induced by Viruses and IFNs and Displays Potent Antiviral Activity against Select Virus Infections In Vivo

机译:Lambda干扰素(IFN-λ),一种III型IFN,由病毒和IFN诱导,并显示出对选定病毒感染的有效抗病毒活性

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摘要

Type III interferons (IFNs) (interleukin-28/29 or lambda interferon [IFN-λ]) are cytokines with IFN-like activities. Here we show that several classes of viruses induce expression of IFN-λ1 and -λ2/3 in similar patterns. The IFN-λs were—unlike alpha/beta interferon (IFN-α/β)—induced directly by stimulation with IFN-α or -λ, thus identifying type III IFNs as IFN-stimulated genes. In vitro assays revealed that IFN-λs have appreciable antiviral activity against encephalomyocarditis virus (EMCV) but limited activity against herpes simplex virus type 2 (HSV-2), whereas IFN-α potently restricted both viruses. Using three murine models for generalized virus infections, we found that while recombinant IFN-α reduced the viral load after infection with EMCV, lymphocytic choriomeningitis virus (LCMV), and HSV-2, treatment with recombinant IFN-λ in vivo did not affect viral load after infection with EMCV or LCMV but did reduce the hepatic viral titer of HSV-2. In a model for a localized HSV-2 infection, we further found that IFN-λ completely blocked virus replication in the vaginal mucosa and totally prevented development of disease, in contrast to IFN-α, which had a more modest antiviral activity. Finally, pretreatment with IFN-λ enhanced the levels of IFN-γ in serum after HSV-2 infection. Thus, type III IFNs are expressed in response to most viruses and display potent antiviral activity in vivo against select viruses. The discrepancy between the observed antiviral activity in vitro and in vivo may suggest that IFN-λ exerts a significant portion of its antiviral activity in vivo via stimulation of the immune system rather than through induction of the antiviral state.
机译:III型干扰素(IFN)(白介素28/29或λ干扰素[IFN-λ])是具有IFN样活性的细胞因子。在这里,我们显示了几类病毒以相似的模式诱导IFN-λ1和-λ2/ 3的表达。与α/β干扰素(IFN-α/β)不同,IFN-λ是通过IFN-α或-λ刺激直接诱导的,因此将III型IFN识别为IFN刺激的基因。体外测定显示,IFN-λs对脑心肌炎病毒(EMCV)具有明显的抗病毒活性,但对2型单纯疱疹病毒(HSV-2)的活性却有限,而IFN-α则有效地限制了这两种病毒。使用三种鼠类模型进行广义病毒感染,我们发现,尽管重组IFN-α降低了EMCV,淋巴细胞性脉络膜脑膜炎病毒(LCMV)和HSV-2感染后的病毒载量,但体内重组IFN-λ的治疗并没有影响病毒感染EMCV或LCMV后可减少负荷,但确实降低了HSV-2的肝病毒滴度。在具有局部HSV-2感染的模型中,我们进一步发现IFN-λ完全阻断了阴道粘膜中的病毒复制,并完全阻止了疾病的发展,而IFN-α具有更适度的抗病毒活性。最后,用IFN-λ预处理可提高HSV-2感染后血清中IFN-γ的水平。因此,III型IFN表达对大多数病毒的应答,并在体内对选定的病毒显示出有效的抗病毒活性。在体外和体内观察到的抗病毒活性之间的差异可能表明,IFN-λ通过刺激免疫系统而不是通过诱导抗病毒状态而在体内发挥了很大一部分抗病毒活性。

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