利用CpG寡核苷酸靶向递送佐剂到交叉呈递树突状细胞的抗clec9a抗体的设计和表征。

IF 3.8 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Sayumi Yamazoe*, Keerthi Sadanala, Qian Zhang, Arvind Rajpal, Tim Sproul, Pavel Strop and Miranda Broz, 
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引用次数: 0

摘要

c型凝集素受体,Clec9a,是一种在交叉呈递的常规树突状细胞(cDC1)上表达的高度特异性受体。这种罕见树突状细胞(dc)的受体特异性,加上它们固有的内化和定位于内吞室的能力,为先天性免疫激动剂的靶向递送提供了独特的机会。通过利用抗clec9a抗体,我们可以特异性地将这些激动剂递送到交叉呈递的cdc,从而增强肿瘤特异性细胞毒性T淋巴细胞(ctl)的交叉启动和扩增。在这项研究中,我们详细介绍了由clec9a靶向抗体和CpG寡脱氧核苷酸(ODNs)组成的创新生物偶联物的设计和表征,该偶联物可激活cDC1表达的toll样受体9 (TLR9)。在体外生成的CD103+ dc (iCD103 dc)、肿瘤细胞和抗原特异性ctl共培养系统中,这些免疫调节生物偶联物在交叉呈递试验中表现出显著的细胞活性,驱动强大的交叉启动。此外,在小鼠疫苗接种试验中,odn靶向递送cDC1在体内表现出靶向依赖性活性。我们的研究结果强调了靶向clec9a的生物偶联物作为一种强大的策略的潜力,通过精确地将佐剂递送到交叉呈递的树突状细胞来增强抗肿瘤免疫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Design and Characterization of an Anti-Clec9a Antibody Armed with CpG Oligonucleotides To Enable Targeted Delivery of Adjuvant to Cross-Presenting Dendritic Cells

Design and Characterization of an Anti-Clec9a Antibody Armed with CpG Oligonucleotides To Enable Targeted Delivery of Adjuvant to Cross-Presenting Dendritic Cells

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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来源期刊
ACS Chemical Biology
ACS Chemical Biology 生物-生化与分子生物学
CiteScore
7.50
自引率
5.00%
发文量
353
审稿时长
3.3 months
期刊介绍: ACS Chemical Biology provides an international forum for the rapid communication of research that broadly embraces the interface between chemistry and biology. The journal also serves as a forum to facilitate the communication between biologists and chemists that will translate into new research opportunities and discoveries. Results will be published in which molecular reasoning has been used to probe questions through in vitro investigations, cell biological methods, or organismic studies. We welcome mechanistic studies on proteins, nucleic acids, sugars, lipids, and nonbiological polymers. The journal serves a large scientific community, exploring cellular function from both chemical and biological perspectives. It is understood that submitted work is based upon original results and has not been published previously.
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