Department of Microbiology, Tokyo Medical University, Shinjuku-ku, Tokyo, 160-8402, Japan.
Virology. 2010 Nov 25;407(2):325-32. doi: 10.1016/j.virol.2010.08.030. Epub 2010 Sep 19.
Natural killer T (NKT) cell activation is responsible for eliminating pathogens. However, the biological functions of NKT cells against influenza virus are not fully understood. We therefore investigated the effects of NKT cells in viral infection using CD1d knockout (KO) mice. When CD1d KO or wild-type (WT) mice were infected with a sub-lethal dosage of the influenza virus, the survival rate of CD1d KO mice was significantly lower than for WT mice in association with delayed viral clearance in the lungs. Consistently, IFN-γ production in bronchoalveolar lavage fluid of CD1d KO mice was largely reduced compared to WT mice during infection. Moreover, the cytotoxic activities of NK cells and viral antigen-specific CD8(+) T cells were impaired in CD1d KO mice. It was concluded that activated NKT cell-induced IFN-γ release enhances both NK-cell activity and antigen-specific CD8(+) T cells to eliminate the influenza virus, thus leading to an enhanced survival.
自然杀伤 T (NKT) 细胞的激活负责清除病原体。然而,NKT 细胞对流感病毒的生物学功能尚不完全清楚。因此,我们使用 CD1d 敲除 (KO) 小鼠研究了 NKT 细胞在病毒感染中的作用。当 CD1d KO 或野生型 (WT) 小鼠感染低致死剂量的流感病毒时,与 WT 小鼠相比,CD1d KO 小鼠的存活率明显较低,与肺部病毒清除延迟有关。一致地,与 WT 小鼠相比,在感染期间,CD1d KO 小鼠支气管肺泡灌洗液中的 IFN-γ 产生大大减少。此外,NK 细胞和病毒抗原特异性 CD8(+) T 细胞的细胞毒性活性在 CD1d KO 小鼠中受损。结论是,激活的 NKT 细胞诱导 IFN-γ 释放增强了 NK 细胞的活性和病毒特异性 CD8(+) T 细胞,以消除流感病毒,从而提高了存活率。