Cervantes-Barragan Luisa, Züst Roland, Weber Friedemann, Spiegel Martin, Lang Karl S, Akira Shizuo, Thiel Volker, Ludewig Burkhard
Research Department, Kantonal Hospital St Gallen, Switzerland, and Abeteilung Virologie, Institut fur Medizinische Mikrobiologie und Hygiene, Universitat Freiburg, Germany.
Blood. 2007 Feb 1;109(3):1131-7. doi: 10.1182/blood-2006-05-023770. Epub 2006 Sep 19.
This study demonstrates a unique and crucial role of plasmacytoid dendritic cells (pDCs) and pDC-derived type I interferons (IFNs) in the pathogenesis of mouse coronavirus infection. pDCs controlled the fast replicating mouse hepatitis virus (MHV) through the immediate production of type I IFNs. Recognition of MHV by pDCs was mediated via TLR7 ensuring a swift IFN-alpha production following encounter with this cytopathic RNA virus. Furthermore, the particular type I IFN response pattern was not restricted to the murine coronavirus, but was also found in infection with the highly cytopathic human severe acute respiratory syndrome (SARS) coronavirus. Taken together, our results suggest that rapid production of type I IFNs by pDCs is essential for the control of potentially lethal coronavirus infections.
本研究证明了浆细胞样树突状细胞(pDCs)和pDC来源的I型干扰素(IFNs)在小鼠冠状病毒感染发病机制中具有独特且关键的作用。pDCs通过立即产生I型干扰素来控制快速复制的小鼠肝炎病毒(MHV)。pDCs对MHV的识别是通过TLR7介导的,确保在遇到这种细胞病变RNA病毒后迅速产生α干扰素。此外,特定的I型干扰素反应模式不仅限于鼠冠状病毒,在感染高致病性人类严重急性呼吸综合征(SARS)冠状病毒时也有发现。综上所述,我们的结果表明,pDCs快速产生I型干扰素对于控制潜在致命的冠状病毒感染至关重要。