Dessing Mark C, van der Sluijs Koenraad F, Florquin Sandrine, van der Poll Tom
Center of Infection and Immunity Amsterdam (CINIMA), University of Amsterdam, The Netherlands.
Clin Immunol. 2007 Dec;125(3):328-36. doi: 10.1016/j.clim.2007.08.001. Epub 2007 Sep 10.
Monocyte chemoattractant protein 1 (MCP-1) and its receptor CCR2 have been shown to play an import role in leukocyte recruitment to sites of infection and inflammation. To investigate the role of MCP-1 during infection with influenza we inoculated wild-type (WT) and MCP-1 knockout (KO) mice with a non-lethal dose of a mouse adapted strain of influenza A. Influenza infection of WT mice resulted in a profound increase in pulmonary MCP-1 levels. MCP-1 KO mice had enhanced weight loss and did not fully regain their body weight during the 14-day observation period. In addition, MCP-1 KO mice demonstrated elevated viral loads 8 days after infection, which was accompanied by reduced leukocyte recruitment into the infected lungs, primarily caused by a diminished influx of macrophages and granulocytes. Moreover, pulmonary levels of IgA were reduced in MCP-1 KO mice. The pulmonary concentrations of tumor necrosis factor-alpha, interleukin-6, macrophage inflammatory protein 2 and interferon-gamma were higher in MCP-1 KO mice. This study shows that MCP-1 contributes to an adequate protective immune response against influenza infection in mice.
单核细胞趋化蛋白1(MCP-1)及其受体CCR2已被证明在白细胞募集到感染和炎症部位中发挥重要作用。为了研究MCP-1在流感感染过程中的作用,我们用非致死剂量的适应小鼠的甲型流感病毒株接种野生型(WT)和MCP-1基因敲除(KO)小鼠。WT小鼠感染流感后,肺中MCP-1水平显著升高。MCP-1 KO小鼠体重减轻加剧,在14天的观察期内未完全恢复体重。此外,MCP-1 KO小鼠在感染后8天病毒载量升高,同时进入感染肺部的白细胞募集减少,这主要是由于巨噬细胞和粒细胞流入减少所致。而且,MCP-1 KO小鼠肺中IgA水平降低。MCP-1 KO小鼠肺中肿瘤坏死因子-α、白细胞介素-6、巨噬细胞炎性蛋白2和干扰素-γ的浓度较高。这项研究表明,MCP-1有助于小鼠对流感感染产生充分的保护性免疫反应。