呼吸系统
免疫学
接种疫苗
限制
鼻腔给药
抗原
病毒学
抗体
医学
呼吸道
生物
免疫
受体
免疫系统
抗原呈递
粘膜免疫学
粘膜
T细胞
抗体反应
病毒感染
微生物学
呼吸道感染
呼吸道疾病
粘膜免疫
病毒
减毒疫苗
疫苗效力
免疫
细胞
呼吸道感染
淋巴系统
作者
Haibo Zhang,Katharine Floyd,Zhuoqing Fang,Filipe Araujo Hoffmann,Audrey Lee,Heather Marie Froggatt,Gurpreet Bharj,Xia Xie,Haleigh B. Eppler,Jordan Mariah Santagata,Yanli Wang,M. J. C. Hu,Christopher B. Fox,Prabhu S. Arunachalam,Ralph Baric,Mehul S. Suthar,Bali Pulendran
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-02-19
卷期号:: eaea1260-eaea1260
被引量:3
标识
DOI:10.1126/science.aea1260
摘要
memory T cells that imprinted alveolar macrophages (AMs), enhancing antigen presentation and antiviral immunity. Following infection, vaccinated mice mounted rapid pathogen-specific T cell and antibody responses and formed ectopic lymphoid structures in the lung. These results reveal a class of "universal vaccines" against diverse respiratory threats.
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