Xu Yang, Masuda Kazuya, Groso Christine, Hassan Rick, Zhou Ziyou, Broderick Kelsey, Tsuji Moriya, Tison Christopher
Luna Labs USA, LLC, Charlottesville, VA 22903, USA.
Aaron Diamond AIDS Research Center, Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA.
Vaccines (Basel). 2024 Mar 21;12(3):339. doi: 10.3390/vaccines12030339.
The COVID-19 outbreak was a global pandemic with wide-ranging healthcare implications. Although several mRNA-based vaccines delivered using lipid nanoparticles (LNP) have been approved and demonstrated efficacy at reducing the severity and spread of infection, continued rapid viral evolution and disadvantages currently associated with LNP delivery vehicles (such as toxicity) are driving the design of next-generation SARS-CoV-2 vaccines. Herein, we describe the development of a trimethylated chitosan-based nanoparticle layer-by-layer (LbL) delivery platform for multiple antigens as a scalable and safe COVID-19 vaccine, known as, "LbL-CoV19". These vaccine candidates have been demonstrated to be biocompatible, safe, and effective at stimulating both humoral and cellular responses for protection in preclinical studies. Preliminary results also indicate that LbL-CoV19 can potentially achieve rapid, long-lasting, and broad protection against the SARS-CoV-2 challenge. The "plug-and-play" platform technology is well suited to preparedness for future pandemics and disease outbreaks.
新冠疫情是一场具有广泛医疗影响的全球大流行。尽管几种使用脂质纳米颗粒(LNP)递送的基于mRNA的疫苗已获批准,并在降低感染的严重程度和传播方面显示出疗效,但病毒的持续快速进化以及目前与LNP递送载体相关的缺点(如毒性)正在推动下一代新冠病毒疫苗的设计。在此,我们描述了一种基于三甲基壳聚糖的纳米颗粒逐层(LbL)递送平台,用于递送多种抗原,作为一种可扩展且安全的新冠疫苗,称为“LbL-CoV19”。在临床前研究中,这些候选疫苗已被证明具有生物相容性、安全性,并且在刺激体液和细胞反应以提供保护方面是有效的。初步结果还表明,LbL-CoV19有可能实现对新冠病毒攻击的快速、持久和广泛保护。这种“即插即用”的平台技术非常适合应对未来的大流行和疾病爆发。