Infusini Giuseppe, Smith Jeffrey M, Yuan He, Pizzolla Angela, Ng Wy Ching, Londrigan Sarah L, Haque Ashraful, Reading Patrick C, Villadangos Jose A, Wakim Linda M
Division of Systems Biology and Personalised Medicine, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3052, Australia.
Department of Microbiology and Immunology, The University of Melbourne, at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria 3000, Australia.
PLoS One. 2015 Nov 23;10(11):e0143539. doi: 10.1371/journal.pone.0143539. eCollection 2015.
Respiratory dendritic cells (DC) play a pivotal role in the initiation of adaptive immune responses to influenza virus. To do this, respiratory DCs must ferry viral antigen from the lung to the draining lymph node without becoming infected and perishing en route. We show that respiratory DCs up-regulate the expression of the antiviral molecule, interferon-induced transmembrane protein 3 (IFITM3) in response to influenza virus infection, in a manner dependent on type I interferon signaling and the transcription factors IRF7 and IRF3. Failure of respiratory DCs to up-regulate IFITM3 following influenza virus infection resulted in impaired trafficking to the draining LN and consequently in impaired priming of an influenza-specific CD8+ T cell response. The impaired trafficking of IFITM3-deficient DC correlated with an increased susceptibility of these DC to influenza virus infection. This work shows that the expression of IFITM3 protects respiratory DCs from influenza virus infection, permitting migration from lung to LN and optimal priming of a virus specific T-cell response.
呼吸道树突状细胞(DC)在启动针对流感病毒的适应性免疫反应中起关键作用。为此,呼吸道DC必须将病毒抗原从肺部转运至引流淋巴结,而不会在途中被感染并死亡。我们发现,呼吸道DC在受到流感病毒感染后会上调抗病毒分子干扰素诱导跨膜蛋白3(IFITM3)的表达,其方式依赖于I型干扰素信号传导以及转录因子IRF7和IRF3。流感病毒感染后呼吸道DC未能上调IFITM3,导致其向引流淋巴结的转运受损,进而导致流感特异性CD8 + T细胞反应的启动受损。IFITM3缺陷型DC转运受损与这些DC对流感病毒感染的易感性增加相关。这项研究表明,IFITM3的表达可保护呼吸道DC免受流感病毒感染,使其能够从肺部迁移至淋巴结,并对病毒特异性T细胞反应进行最佳启动。