纳米载体
重编程
纳米囊
免疫系统
免疫
体内
肺
生物
纳米技术
免疫学
获得性免疫系统
细胞生物学
药物输送
先天免疫系统
癌症研究
免疫原性
纳米毒理学
蛋白质稳定性
计算生物学
免疫疗法
医学
细胞
化学
蛋白质-蛋白质相互作用
作者
Luyao Wang,Wen Zhou,Hang Chen,Xiangqian Jia,Peiyuan Zheng,Haolin Jiang,Mengling Wu,Yaning Zhang,Yanchao Ding,Juanjuan Du
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-08-24
卷期号:20 (35): 24401-24414
标识
DOI:10.1021/acsnano.6c05606
摘要
Effective lung-targeted therapies can directly treat pulmonary diseases and engage tissue-resident immunity for lasting effects. However, protein delivery systems specifically targeting the lung remain scarce. Here, we report the discovery of phenylborate (PBA)-functionalized polymeric nanocapsules that enable efficient pulmonary delivery of protein cargos following systemic administration. Systematic structure-activity relationship studies revealed that PBA incorporation strongly correlates with enhanced lung tropism, establishing a previously unrecognized materials design principle for lung-targeted protein delivery. Leveraging this capability, we demonstrate that lung-targeted antigen delivery induces robust tissue-resident memory T cell responses within the pulmonary microenvironment and suppresses tumor growth in preclinical models of lung metastasis. Together, these findings redefine the in vivo functional role of phenylborate in nanocarrier systems and establish a versatile materials platform for lung-targeted protein therapeutics and site-specific immune modulation.
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