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A self-assembled trimeric protein vaccine induces protective immunity against Omicron variant.

Cai HeJingyun YangWeiqi HongZimin ChenDandan PengHong LeiAqu AluXuemei HeZhenfei BiXiaohua JiangGuowen JiaYun YangYanan ZhouWenhai YuCong TangQing HuangMengli YangBai LiJingmei LiJunbin WangHaiying QueLi ChenWenyan RenDandan WanJiong LiWei WangGuobo ShenZhiwei ZhaoLi YangJinliang YangZhenling WangZhaoming SuYuquan WeiXiaobo CenYoshimasa TanakaXiangrong SongShuai-Yao LuXiaozhong PengGuang-Wen LuYanping Qian
Published in: Nature communications (2022)
The recently emerged Omicron (B.1.1.529) variant has rapidly surpassed Delta to become the predominant circulating SARS-CoV-2 variant, given the higher transmissibility rate and immune escape ability, resulting in breakthrough infections in vaccinated individuals. A new generation of SARS-CoV-2 vaccines targeting the Omicron variant are urgently needed. Here, we developed a subunit vaccine named RBD-HR/trimer by directly linking the sequence of RBD derived from the Delta variant (containing L452R and T478K) and HR1 and HR2 in SARS-CoV-2 S2 subunit in a tandem manner, which can self-assemble into a trimer. In multiple animal models, vaccination of RBD-HR/trimer formulated with MF59-like oil-in-water adjuvant elicited sustained humoral immune response with high levels of broad-spectrum neutralizing antibodies against Omicron variants, also inducing a strong T cell immune response in vivo. In addition, our RBD-HR/trimer vaccine showed a strong boosting effect against Omicron variants after two doses of mRNA vaccines, featuring its capacity to be used in a prime-boost regimen. In mice and non-human primates, RBD-HR/trimer vaccination could confer a complete protection against live virus challenge of Omicron and Delta variants. The results qualified RBD-HR/trimer vaccine as a promising next-generation vaccine candidate for prevention of SARS-CoV-2, which deserved further evaluation in clinical trials.
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