Department of Pathology, New York University School of Medicine, New York, NY 10016, USA.
Immunol Rev. 2013 Sep;255(1):25-39. doi: 10.1111/imr.12101.
Interferons (IFNs) are produced in response to virus infection and induce an antiviral state in virtually all cell types. In addition to upregulating the transcription of genes that inhibit virus replication, type I (or -α/β) IFNs also act to orchestrate the adaptive immune response to virus infection. Recently a new family of antiviral cytokines, the type III (or -λ) IFNs, has been identified that activate the same antiviral pathways via a distinct receptor. Although the identical transcription factor, IFN-stimulated gene factor 3 is activated by either IFN-α/β or IFN-λ signaling, differences in the induction and action of these two cytokine families are beginning to be appreciated. In this article, we review this emerging body of literature on the differing roles these cytokines play in host defense of the mucosal surface. Although many viruses enter the body through the respiratory and gastrointestinal tracts, we have focused the discussion on influenza A virus, respiratory syncytial virus, and rotavirus, three ubiquitous human pathogens that target the epithelial lining and are associated with a major disease burden.
干扰素(IFNs)是在病毒感染后产生的,几乎能在所有细胞类型中诱导抗病毒状态。除了上调抑制病毒复制的基因转录外,I 型(或-α/β)IFNs 还能协调针对病毒感染的适应性免疫反应。最近,一个新的抗病毒细胞因子家族,即 III 型(或-λ)IFNs,已被鉴定出来,它通过一个独特的受体激活相同的抗病毒途径。虽然相同的转录因子干扰素刺激基因因子 3(IFN-stimulated gene factor 3)被 IFN-α/β 或 IFN-λ 信号激活,但这两种细胞因子家族的诱导和作用的差异开始被认识到。在本文中,我们回顾了这一新兴的文献,探讨了这些细胞因子在宿主防御黏膜表面方面的不同作用。尽管许多病毒通过呼吸道和胃肠道进入人体,但我们将讨论重点放在了甲型流感病毒、呼吸道合胞病毒和轮状病毒上,这三种普遍存在的人类病原体都以上皮衬里为靶点,并与重大疾病负担有关。