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连接化学和连接性精细调节共轭 NOD2/TLR7 激动剂的免疫反应和动力学溶解度。

Linker Chemistry and Connectivity Fine-Tune the Immune Response and Kinetic Solubility of Conjugated NOD2/TLR7 Agonists.

机构信息

Faculty of Pharmacy, University of Ljubljana, SI-1000 Ljubljana, Slovenia.

出版信息

Bioconjug Chem. 2024 Nov 20;35(11):1723-1731. doi: 10.1021/acs.bioconjchem.4c00321. Epub 2024 Oct 10.

Abstract

There is a growing interest in developing novel immune potentiators capable of eliciting a cellular immune response. We tackle this challenge by harnessing the synergistic cross-activation between two innate immune receptors─the nucleotide-binding oligomerization domain-containing protein 2 (NOD2) and Toll-like receptor 7 (TLR7). Herein, we investigate the structure-activity relationship of a series of novel conjugated NOD2/TLR7 agonists incorporating a variety of flexible aliphatic, poly(ethylene glycol)-based and triazole-featuring linkers. Our findings reveal potent immune-enhancing properties of conjugates in human primary peripheral blood mononuclear cells, characterized by a Th1/Th17 polarized cytokine response. Importantly, we demonstrate that both the chemistry of the linker and the site of linkage affect the immune fingerprint and the kinetic solubility of these conjugated agonists. These results shed further light on the immunostimulatory potential of NOD2/TLR7 cross-activation and provide insights for designing innovative immune potentiators.

摘要

人们越来越关注开发能够引发细胞免疫反应的新型免疫增强剂。我们通过利用两种先天免疫受体——核苷酸结合寡聚化结构域蛋白 2(NOD2)和 Toll 样受体 7(TLR7)之间的协同交叉激活来应对这一挑战。在此,我们研究了一系列新型共轭 NOD2/TLR7 激动剂的结构-活性关系,其中包含各种灵活的脂肪族、聚(乙二醇)基和三唑基连接子。我们的研究结果揭示了这些共轭物在人外周血单核细胞中的强大免疫增强特性,表现为 Th1/Th17 极化细胞因子反应。重要的是,我们证明了连接子的化学性质和连接点都会影响这些共轭激动剂的免疫指纹和动力学溶解度。这些结果进一步揭示了 NOD2/TLR7 交叉激活的免疫刺激潜力,并为设计创新的免疫增强剂提供了思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bb1/11583123/3fb08ebe5b3a/bc4c00321_0001.jpg

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