| Literature DB >> 33649323 |
Joshua G Liang1, Danmei Su1, Tian-Zhang Song2, Yilan Zeng3, Weijin Huang4, Jinhua Wu1, Rong Xu1, Peiwen Luo1, Xiaofang Yang1, Xiaodong Zhang1, Shuangru Luo1, Ying Liang1, Xinglin Li1, Jiaju Huang1, Qiang Wang1, Xueqin Huang1, Qingsong Xu1, Mei Luo3, Anliang Huang5, Dongxia Luo3, Chenyan Zhao4, Fan Yang5, Jian-Bao Han2, Yong-Tang Zheng2, Peng Liang6.
Abstract
SARS-CoV-2 is the underlying cause for the COVID-19 pandemic. Like most enveloped RNA viruses, SARS-CoV-2 uses a homotrimeric surface antigen to gain entry into host cells. Here we describe S-Trimer, a native-like trimeric subunit vaccine candidate for COVID-19 based on Trimer-Tag technology. Immunization of S-Trimer with either AS03 (oil-in-water emulsion) or CpG 1018 (TLR9 agonist) plus alum adjuvants induced high-level of neutralizing antibodies and Th1-biased cellular immune responses in animal models. Moreover, rhesus macaques immunized with adjuvanted S-Trimer were protected from SARS-CoV-2 challenge compared to vehicle controls, based on clinical observations and reduction of viral loads in lungs. Trimer-Tag may be an important platform technology for scalable production and rapid development of safe and effective subunit vaccines against current and future emerging RNA viruses.Entities:
Year: 2021 PMID: 33649323 DOI: 10.1038/s41467-021-21634-1
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919