| Literature DB >> 34059617 |
Ren Yang1, Yao Deng1, Baoying Huang1, Lei Huang2, Ang Lin2, Yuhua Li3, Wenling Wang1, Jingjing Liu3, Shuaiyao Lu4, Zhenzhen Zhan5, Yufei Wang6,7, Ruhan A1, Wen Wang1, Peihua Niu1, Li Zhao1, Shiqiang Li2, Xiaopin Ma2, Luyao Zhang2, Yujian Zhang2, Weiguo Yao2, Xingjie Liang6,7, Jincun Zhao8, Zhongmin Liu5, Xiaozhong Peng9, Hangwen Li10, Wenjie Tan11,12.
Abstract
Although inoculation of COVID-19 vaccines has rolled out globally, there is still a critical need for safe and effective vaccines to ensure fair and equitable supply for all countries. Here, we report on the development of a highly efficacious mRNA vaccine, SW0123 that is composed of sequence-modified mRNA encoding the full-length SARS-CoV-2 Spike protein packaged in core-shell structured lipopolyplex (LPP) nanoparticles. SW0123 is easy to produce using a large-scale microfluidics-based apparatus. The unique core-shell structured nanoparticle facilitates vaccine uptake and demonstrates a high colloidal stability, and a desirable biodistribution pattern with low liver targeting effect upon intramuscular administration. Extensive evaluations in mice and nonhuman primates revealed strong immunogenicity of SW0123, represented by induction of Th1-polarized T cell responses and high levels of antibodies that were capable of neutralizing not only the wild-type SARS-CoV-2, but also a panel of variants including D614G and N501Y variants. In addition, SW0123 conferred effective protection in both mice and non-human primates upon SARS-CoV-2 challenge. Taken together, SW0123 is a promising vaccine candidate that holds prospects for further evaluation in humans.Entities:
Year: 2021 PMID: 34059617 DOI: 10.1038/s41392-021-00634-z
Source DB: PubMed Journal: Signal Transduct Target Ther ISSN: 2059-3635