The safety, immunogenicity, and efficacy of heterologous boosting with a SARS-CoV-2 mRNA vaccine (SYS6006) in Chinese participants aged 18 years or more: a randomized, open-label, active-controlled phase 3 trial

被引:2
|
作者
Zhou, Chunhua [1 ,2 ]
Qiu, Yuanzheng [3 ]
Wang, Jianxin [1 ,2 ]
Zhong, Xiang [3 ]
Zhu, Xiufang [1 ]
Huang, Xiaojing [1 ]
Yang, Lan [1 ]
Ji, Qiaolei [3 ]
Zhou, Feifei [3 ]
Wu, Shunquan [3 ]
Yang, Mengjie [4 ]
Zhang, Jing [4 ]
Liu, Kaili [3 ]
Ji, Li [3 ]
Yang, Hanyu [3 ]
Li, Chunlei [3 ,5 ]
Zhao, Yuanyuan [1 ,6 ]
机构
[1] Hebei Med Univ, Hosp 1, Dept Clin Pharm, Shijiazhuang, Peoples R China
[2] Technol Innovat Ctr Artificial Intelligence Clin P, Shijiazhuang, Peoples R China
[3] CSPC Megalith Biopharmaceut Co Ltd, Shijiazhuang, Peoples R China
[4] Chinese Ctr Dis Control & Prevent, Natl Inst Viral Dis Control & Prevent, NHC Key Lab Biosafety, Beijing, Peoples R China
[5] CSPC Megalith Biopharmaceut Co Ltd, Shijiazhuang 050011, Hebei, Peoples R China
[6] Hebei Med Univ, Hosp 1, Dept Clin Pharm, Shijiazhuang 050031, Hebei, Peoples R China
关键词
SARS-CoV-2; mRNA vaccine; heterologous boosting; safety; immunogenicity; efficacy; COVID-19; VACCINE; BLIND;
D O I
10.1080/22221751.2024.2320913
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Continuous emergence of new variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), enhanced transmissibility, significant immune escape, and waning immunity call for booster vaccination. We evaluated the safety, immunogenicity, and efficacy of heterologous booster with a SARS-CoV-2 mRNA vaccine SYS6006 versus an active control vaccine in a randomized, open-label, active-controlled phase 3 trial in healthy adults aged 18 years or more who had received two or three doses of SARS-CoV-2 inactivated vaccine in China. The trial started in December 2022 and lasted for 6 months. The participants were randomized (overall ratio: 3:1) to receive one dose of SYS6006 (N = 2999) or an ancestral receptor binding region-based, alum-adjuvanted recombinant protein SARS-CoV-2 vaccine (N = 1000), including 520 participants in an immunogenicity subgroup. SYS6006 boosting showed good safety profiles with most AEs being grade 1 or 2, and induced robust wild-type and Omicron BA.5 neutralizing antibody response on Days 14 and 28, demonstrating immunogenicity superiority versus the control vaccine and meeting the primary objective. The relative vaccine efficacy against COVID-19 of any severity was 51.6% (95% CI, 35.5-63.7) for any variant, 66.8% (48.6-78.5) for BA.5, and 37.7% (2.4-60.3) for XBB, from Day 7 through Month 6. In the vaccinated and infected hybrid immune participants, the relative vaccine efficacy was 68.4% (31.1-85.5) against COVID-19 of any severity caused by a second infection. All COVID-19 cases were mild. SYS6006 heterologous boosting demonstrated good safety, superior immunogenicity and high efficacy against BA.5-associated COVID-19, and protected against XBB-associated COVID-19, particularly in the hybrid immune population.Trial registration: Chinese Clinical Trial Registry: ChiCTR2200066941
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页数:12
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