Affiliation:
1. Department of Otolaryngology the Sixth Affiliated Hospital of Sun Yat‐sen University Guangzhou Guangdong 510655 China
2. Biomedical Innovation Center The Sixth Affiliated Hospital Sun Yat‐sen University Guangzhou Guangdong 510655 China
3. Department of Biomedical Engineering Columbia University New York NY 10027 USA
4. Department of Otolaryngology the First Affiliated Hospital of Sun Yat‐sen University Guangzhou Guangdong 510080 China
Abstract
AbstractDespite the promising achievements of immune checkpoint blockade (ICB) therapy for tumor treatment, its therapeutic effect against solid tumors is limited due to the suppressed tumor immune microenvironment (TIME). Herein, a series of polyethyleneimine (Mw = 0.8k, PEI0.8k)‐covered MoS2 nanosheets with different sizes and charge densities are synthesized, and the CpG, a toll‐like receptor‐9 agonist, is enveloped to construct nanoplatforms for the treatment of head and neck squamous cell carcinoma (HNSCC). It is proved that functionalized nanosheets with medium size display similar CpG loading capacity regardless of low or high PEI0.8k coverage owing to the flexibility and crimpability of 2D backbone. CpG‐loaded nanosheets with medium size and low charge density (CpG@MM‐PL) could promote the maturation, antigen‐presenting capacity, and proinflammatory cytokines generation of bone marrow‐derived dendritic cells (DCs). Further analysis reveals that CpG@MM‐PL effectively boosts the TIME of HNSCC in vivo including DC maturation and cytotoxic T lymphocyte infiltration. Most importantly, the combination of CpG@MM‐PL and ICB agents anti‐programmed death 1 hugely improves the tumor therapeutic effect, inspiring more attempts for cancer immunotherapy. In addition, this work uncovers a pivotal feature of the 2D sheet‐like materials in nanomedicine development, which should be considered for the design of future nanosheet‐based therapeutic nanoplatforms.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Guangdong Province
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献