抗原
细胞毒性T细胞
CD8型
T细胞
生物
抗原呈递
甲型流感病毒
免疫学
抗原提呈细胞
肺
病毒学
病毒
免疫系统
医学
体外
内科学
生物化学
作者
Takumi Kawasaki,Moe Ikegawa,Kosuke Yunoki,Hifumi Otani,Daisuke Ori,Ken J. Ishii,Etsushi Kuroda,Shiki Takamura,Masahiro Kitabatake,Toshihiro Ito,Ayako Isotani,Taro Kawai
出处
期刊:Cell Reports
[Elsevier]
日期:2022-12-01
卷期号:41 (11): 111828-111828
被引量:13
标识
DOI:10.1016/j.celrep.2022.111828
摘要
Lung CD8+ memory T cells play central roles in protective immunity to respiratory viruses, such as influenza A virus (IAV). Here, we find that alveolar macrophages (AMs) function as antigen-presenting cells that support the expansion of lung CD8+ memory T cells. Intranasal antigen administration to mice subcutaneously immunized with antigen results in a rapid expansion of antigen-specific CD8+ T cells in the lung, which is dependent on antigen cross-presentation by AMs. AMs highly express interleukin-18 (IL-18), which mediates subsequent formation of CD103+CD8+ resident memory T (TRM) cells in the lung. In a mouse model of IAV infection, AMs are required for expansion of virus-specific CD8+ T cells and CD103+CD8+ TRM cells and inhibiting virus replication in the lungs during secondary infection. These results suggest that AMs instruct a rapid expansion of antigen-specific CD8+ T cells in lung, which protect the host from respiratory virus infection.
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