免疫系统
巨噬细胞
牙龈卟啉单胞菌
牙周炎
微生物学
先天免疫系统
TLR2型
炎症
吞噬作用
细胞因子
化学
免疫学
生物
体外
医学
生物化学
内科学
作者
Na Yan,Junchao Xu,Guolin Liu,Chao Ma,Lin Bao,Yalin Cong,Ziyao Wang,Yuliang Zhao,Weihua Xu,Chunying Chen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-10-26
卷期号:16 (11): 18253-18265
被引量:42
标识
DOI:10.1021/acsnano.2c05923
摘要
Periodontitis is a chronic inflammatory disease caused by the interaction of oral microorganisms with the host immune response. Porphyromonas gingivalis (P.g.) acts as a key mediator in subverting the homeostasis of the local immune system. On the one hand, P.g. inhibits phagocytosis and the killing capacity of immune cells. On the other hand, P.g. increases selective cytokine release, which is beneficial to its further proliferation. Here, we prepared a penetrating macrophage-based nanoformulation (MZ@PNM)-encapsulating hydrogel (MZ@PNM@GCP) that responded to the periodontitis microenvironment. MZ@PNM targeted P.g. via the Toll-like receptor complex 2/1 (TLR2/1) on its macrophage-mimicking membrane, then directly killed P.g. through disruption of bacterial structural integrity by the cationic nanoparticles and intracellular release of an antibacterial drug, metronidazole (MZ). Meanwhile, MZ@PNM interrupted the specific binding of P.g. to immune cells and neutralized complement component 5a (C5a), preventing P.g. subversion of periodontal host immune response. Overall, MZ@PNM@GCP showed potent efficacy in periodontitis treatment, restoring local immune function and killing pathogenic bacteria, while exhibiting favorable biocompatibility, all of which have been demonstrated both in vivo and in vitro.
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