Langland Jeffrey O, Cameron Jason M, Heck Michael C, Jancovich James K, Jacobs Bertram L
Center for Infectious Disease and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, AZ 85287-5401, USA.
Virus Res. 2006 Jul;119(1):100-10. doi: 10.1016/j.virusres.2005.10.014. Epub 2006 May 15.
Interferons were the first of the anti-viral innate immune modulators to be characterized, initially characterized solely as anti-viral proteins [reviewed in Le Page, C., Genin, P., Baines, M.G., Hiscott, J., 2000. Inteferon activation and innate immunity. Rev. Immunogenet. 2, 374-386]. As we have progressed in our understanding of the interferons they have taken a more central role in our understanding of innate immunity and its interplay with the adaptive immune response. One of the key players in function of interferon is the interferon-inducible enzyme, protein kinase (PKR, activatable by RNA). The key role played by PKR in the innate response to virus infection is emphasized by the large number of viruses, DNA viruses as well as RNA viruses, whose hosts range from insects to humans, that code for PKR inhibitors. In this review we will first describe activation of PKR and then describe the myriad of ways that viruses inhibit function of PKR.
干扰素是最早被鉴定的抗病毒天然免疫调节剂,最初仅被鉴定为抗病毒蛋白[见Le Page, C., Genin, P., Baines, M.G., Hiscott, J., 2000年。干扰素激活与天然免疫。免疫遗传学评论。2, 374 - 386]。随着我们对干扰素理解的深入,它们在我们对天然免疫及其与适应性免疫反应相互作用的理解中发挥了更核心的作用。干扰素功能的关键参与者之一是干扰素诱导酶,蛋白激酶(PKR,可被RNA激活)。大量病毒(包括DNA病毒和RNA病毒,宿主范围从昆虫到人类)编码PKR抑制剂,这突出了PKR在病毒感染天然反应中的关键作用。在本综述中,我们将首先描述PKR的激活,然后描述病毒抑制PKR功能的多种方式。