细胞生物学
体内
脾脏
树突状细胞
CD11c公司
流式细胞术
FOXP3型
分子生物学
白细胞介素2受体
免疫系统
卵清蛋白
化学
生物
T细胞
免疫学
生物化学
表型
生物技术
基因
作者
Sebastian Sterling,Svjetlana Kireta,Steven J. P. McInnes,Francis D. Kette,Kisha N. Sivanathan,Juewan Kim,Eduardo J. Cueto‐Díaz,Frédérique Cunin,Jean‐Olivier Durand,Chris Drogemuller,Robert Carroll,Nicolas H. Voelcker,Patrick T. Coates
出处
期刊:ACS Nano
[American Chemical Society]
日期:2018-07-06
卷期号:12 (7): 6637-6647
被引量:55
标识
DOI:10.1021/acsnano.8b01625
摘要
Porous silicon nanoparticles (pSiNP), modified to target dendritic cells (DC), provide an alternate strategy for the delivery of immunosuppressive drugs. Here, we aimed to develop a DC-targeting pSiNP displaying c-type lectin, dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin (DC-SIGN), and CD11c monoclonal antibodies. The in vivo tracking of these fluorescent DC-targeting nanoparticles was assessed in both C57BL/6 mice and common marmosets (Callithrix jacchus) by intravenous injection (20 mg/kg). Rapamycin and ovalbumin (OVA)323–339 peptide loaded pSiNP were employed to evaluate their ability to generate murine CD4+CD25+FoxP3+ regulatory T-cells in vivo within OVA sensitized mice. In vivo, pSiNP migrated to the liver, kidneys, lungs, and spleen in both mice and marmosets. Flow cytometry confirmed pSiNP uptake by splenic and peripheral blood DC when functionalized with targeting antibodies. C57BL/6 OVA sensitized mice injected with CD11c-pSiNP loaded with rapamycin + OVA323–339 produced a 5-fold higher number of splenic regulatory T-cells compared to control mice, at 40 days post-pSiNP injection. These results demonstrate the importance of the immobilized targeting antibodies to enhance cellular uptake and enable the in vivo generation of splenic regulatory T-cells.
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