医学
呼吸系统
刺激
淋巴系统
免疫
淋巴组织
肺癌
肺
药理学
免疫学
免疫系统
肿瘤科
内科学
作者
A Rong,Zhaoguo Han,Meifang Zhou,Chaoqun Nie,Mengyuan Zhu,Sijie Cheng,Tianyi Wang,Jing Wang,Zhen Quan,Kaiqi Wang,Shanshan Liu,Xinxin Hu,Haoyu Wang,Jiannan Wang,Yongyi Wu,Yingbo Li
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-11-29
卷期号:10 (48)
标识
DOI:10.1126/sciadv.adp7561
摘要
The currently available immune checkpoint inhibitors (ICIs) often fail to achieve the desired clinical outcomes due to inadequate immune activation, particularly in patients with lung cancer. To reverse this situation, we synthesized inhalable PFCE-C25 nanoemulsions (NEs), which target lymphocyte activation genes (LAG-3) on immune cells within tumor microenvironment and tumor-draining lymph nodes (TDLNs). By combining in vivo 19 F-MR molecular imaging, we investigate the immunological effects of a single low-dose PFCE-C25 NEs in multiple murine lung cancer models, including human immune system (HIS) mouse models, and validated its immunological effects in human TDLNs. The nebulization therapy with PFCE-C25 NEs demonstrated a notable and enduring maturation of dendritic cells (DCs) in TDLNs, leading to systemic immune responses, prolonged survival, the establishment of immune memory, and resistance to tumor rechallenge. Thus, PFCE-C25 NEs successfully demonstrate a promising and efficient approach for enhancing lymphatic transport and sustained activation of antitumor immune responses in lung cancer.
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