交叉展示
TLR9型
树突状细胞
生物
启动(农业)
抗原
免疫系统
佐剂
癌症免疫疗法
细胞毒性T细胞
CpG寡核苷酸
Toll样受体9
细胞生物学
抗原提呈细胞
免疫学
T细胞
体外
免疫疗法
生物化学
基因表达
基因
DNA甲基化
发芽
植物
作者
Sayumi Yamazoe,Keerthi Sadanala,Qian Zhang,Arvind Rajpal,Tim W. Sproul,Pavel Strop,Miranda L. Broz
标识
DOI:10.1021/acschembio.5c00318
摘要
C-type lectin receptor, Clec9a, is a highly specific receptor expressed on cross-presenting conventional dendritic cells (cDC1). This receptor specificity for this rare population of dendritic cells (DCs), combined with their inherent ability to internalize and localize to the endocytic compartment, presents a unique opportunity for targeted delivery of innate immune agonists. By leveraging an anti-Clec9a antibody, we can specifically deliver these agonists to cross-presenting cDCs, thereby enhancing the cross-priming and expansion of tumor-specific cytotoxic T lymphocytes (CTLs). In this study, we detail the design and characterization of innovative bioconjugates composed of a Clec9a-targeting antibody and CpG oligodeoxynucleotides (ODNs), which activate Toll-like receptor 9 (TLR9) expressed by cDC1. These immunomodulatory bioconjugates exhibited significant cellular activity in cross-presentation assays within a coculture system of in vitro generated CD103+ DCs (iCD103 DCs), tumor cells, and antigen specific CTLs, driving robust cross priming. Furthermore, the targeted delivery of ODNs to cDC1 in vivo demonstrated target-dependent activity in a murine vaccination assay. Our findings underscore the potential of Clec9a-targeted bioconjugates as a powerful strategy to enhance antitumor immunity by precisely delivering adjuvants to cross-presenting dendritic cells.
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