An adenovirus-vectored COVID-19 vaccine confers protection from SARS-COV-2 challenge in rhesus macaques

Author:

Feng Liqiang,Wang Qian,Shan ChaoORCID,Yang Chenchen,Feng Ying,Wu Jia,Liu Xiaolin,Zhou Yiwu,Jiang Rendi,Hu Peiyu,Liu Xinglong,Zhang Fan,Li Pingchao,Niu Xuefeng,Liu Yichu,Zheng Xuehua,Luo Jia,Sun Jing,Gu Yingying,Liu Bo,Xu Yongcun,Li Chufang,Pan Weiqi,Zhao JincunORCID,Ke Changwen,Chen Xinwen,Xu TaoORCID,Zhong Nanshan,Guan Suhua,Yuan ZhimingORCID,Chen LingORCID

Abstract

AbstractThe rapid spread of coronavirus SARS-CoV-2 greatly threatens global public health but no prophylactic vaccine is available. Here, we report the generation of a replication-incompetent recombinant serotype 5 adenovirus, Ad5-S-nb2, carrying a codon-optimized gene encoding Spike protein (S). In mice and rhesus macaques, intramuscular injection with Ad5-S-nb2 elicits systemic S-specific antibody and cell-mediated immune (CMI) responses. Intranasal inoculation elicits both systemic and pulmonary antibody responses but weaker CMI response. At 30 days after a single vaccination with Ad5-S-nb2 either intramuscularly or intranasally, macaques are protected against SARS-CoV-2 challenge. A subsequent challenge reveals that macaques vaccinated with a 10-fold lower vaccine dosage (1 × 1010 viral particles) are also protected, demonstrating the effectiveness of Ad5-S-nb2 and the possibility of offering more vaccine dosages within a shorter timeframe. Thus, Ad5-S-nb2 is a promising candidate vaccine and warrants further clinical evaluation.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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