Institute for Research in Biomedicine, Università della Svizzera italiana, Bellinzona, Switzerland.
Graduate School of Cellular and Molecular Sciences, Faculty of Medicine, University of Bern, Bern, Switzerland.
Nat Microbiol. 2019 Nov;4(11):1930-1940. doi: 10.1038/s41564-019-0506-6. Epub 2019 Jul 29.
The early phase of influenza infection occurs in the upper respiratory tract and the trachea, but little is known about the initial events of virus recognition and control of viral dissemination by the immune system. Here, we report that inflammatory dendritic cells (IDCs) are recruited to the trachea shortly after influenza infection through type I interferon-mediated production of the chemokine CCL2. We further show that recruited IDCs express the C-type lectin receptor SIGN-R1, which mediates direct recognition of the virus by interacting with N-linked glycans present in glycoproteins of the virion envelope. Activation of IDCs via SIGN-R1 triggers the production of the chemokines CCL5, CXCL9 and CXCL10, which initiate the recruitment of protective natural killer (NK) cells in the infected trachea. In the absence of SIGN-R1, the recruitment and activation of NK cells is impaired, leading to uncontrolled viral proliferation. In sum, our results provide insight into the orchestration of the early cellular and molecular events involved in immune protection against influenza.
流感感染的早期阶段发生在上呼吸道和气管中,但对于免疫系统识别病毒和控制病毒传播的初始事件知之甚少。在这里,我们报告说,炎性树突状细胞(IDCs)通过 I 型干扰素介导的趋化因子 CCL2 的产生,在流感感染后不久就被招募到气管中。我们进一步表明,被招募的 IDC 表达 C 型凝集素受体 SIGN-R1,该受体通过与病毒包膜糖蛋白中存在的 N 连接糖基相互作用,直接识别病毒。通过 SIGN-R1 激活 IDC 会触发趋化因子 CCL5、CXCL9 和 CXCL10 的产生,从而启动受感染气管中保护性自然杀伤(NK)细胞的募集。在没有 SIGN-R1 的情况下,NK 细胞的募集和激活受损,导致病毒不受控制地增殖。总之,我们的研究结果为阐明针对流感的免疫保护中涉及的早期细胞和分子事件的协调提供了新的认识。