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通过活体成像揭示流感特异性肺驻留记忆 CD8 T 细胞协调的动态景观和保护性免疫。

Dynamic landscapes and protective immunity coordinated by influenza-specific lung-resident memory CD8 T cells revealed by intravital imaging.

机构信息

Department of Pathology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.

University of Minnesota, Department of Microbiology and Immunology and the Center for Immunology, Minneapolis, MN, USA.

出版信息

Immunity. 2024 Aug 13;57(8):1878-1892.e5. doi: 10.1016/j.immuni.2024.06.016. Epub 2024 Jul 22.

Abstract

Lung-tissue-resident memory (T) CD8 T cells are critical for heterosubtypic immunity against influenza virus (IAV) reinfection. How T cells surveil the lung, respond to infection, and interact with other cells remains unresolved. Here, we used IAV infection of mice in combination with intravital and static imaging to define the spatiotemporal dynamics of lung T cells before and after recall infection. CD69CD103 T cells preferentially localized to lung sites of prior IAV infection, where they exhibited patrolling behavior. After rechallenge, lung T cells formed tight clusters in an antigen-dependent manner. Transcriptomic analysis of IAV-specific T cells revealed the expression of several factors that regulate myeloid cell biology. In vivo rechallenge experiments demonstrated that protection elicited by T cells is orchestrated in part by interferon (IFN)-γ-mediated recruitment of inflammatory monocytes into the lungs. Overall, these data illustrate the dynamic landscapes of CD103 lung T cells that mediate early protective immunity against IAV infection.

摘要

肺组织驻留记忆(T)CD8 T 细胞对于异源亚型免疫抵抗流感病毒(IAV)再感染至关重要。T 细胞如何监测肺部、对感染做出反应以及与其他细胞相互作用仍未得到解决。在这里,我们使用 IAV 感染小鼠结合体内和静态成像来定义回忆性感染前后肺 T 细胞的时空动力学。CD69CD103 T 细胞优先定位于先前 IAV 感染的肺部部位,在那里它们表现出巡逻行为。在再次挑战后,肺 T 细胞以抗原依赖性方式形成紧密簇。对 IAV 特异性 T 细胞的转录组分析揭示了几种调节髓样细胞生物学的因子的表达。体内再挑战实验表明,T 细胞引发的保护部分是通过干扰素(IFN)-γ介导将炎症单核细胞募集到肺部来协调的。总体而言,这些数据说明了介导 IAV 感染早期保护性免疫的 CD103 肺 T 细胞的动态景观。

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