Phua Kyle K L
Department of Chemical & Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 3, Singapore 117583.
J Immunol Res. 2015;2015:680620. doi: 10.1155/2015/680620. Epub 2015 Dec 24.
The use of nanoparticles encapsulating messenger RNA (mRNA) as a vaccine has recently attracted much attention because of encouraging results achieved in many nonviral genetic antitumor vaccination studies. Notably, in all of these studies, mRNA nanoparticles are passively targeted to dendritic cells (DCs) through careful selection of vaccination sites. Hence, DC-targeted mRNA nanoparticle vaccines may be an imminent next step forward. In this brief report, we will discuss established conjugation strategies that have been successfully applied to both polymeric and liposomal gene delivery systems. We will also briefly describe promising DC surface receptors amenable for targeting mRNA nanoparticles. Practicable conjugation strategies and receptors reviewed in this paper will provide a convenient reference to facilitate future development of targeted mRNA nanoparticle vaccine.
由于在许多非病毒基因抗肿瘤疫苗接种研究中取得了令人鼓舞的成果,使用包裹信使核糖核酸(mRNA)的纳米颗粒作为疫苗最近备受关注。值得注意的是,在所有这些研究中,通过精心选择疫苗接种部位,mRNA纳米颗粒可被动靶向树突状细胞(DC)。因此,靶向DC的mRNA纳米颗粒疫苗可能是即将迈出的下一步。在本简要报告中,我们将讨论已成功应用于聚合物和脂质体基因递送系统的既定偶联策略。我们还将简要描述适合靶向mRNA纳米颗粒的有前景的DC表面受体。本文中综述的可行偶联策略和受体将提供便利的参考,以促进靶向mRNA纳米颗粒疫苗的未来发展。