ImmunityBio, Inc., Culver City, CA, United States.
IosBio, Burgess Hill, United Kingdom.
Front Immunol. 2021 Sep 16;12:729837. doi: 10.3389/fimmu.2021.729837. eCollection 2021.
We have developed a dual-antigen COVID-19 vaccine incorporating genes for a modified SARS-CoV-2 spike protein (S-Fusion) and the viral nucleocapsid (N) protein with an Enhanced T-cell Stimulation Domain (N-ETSD) to increase the potential for MHC class II responses. The vaccine antigens are delivered by a human adenovirus serotype 5 platform, hAd5 [E1-, E2b-, E3-], previously demonstrated to be effective in the presence of Ad immunity. Vaccination of rhesus macaques with the hAd5 S-Fusion + N-ETSD vaccine by subcutaneous prime injection followed by two oral boosts elicited neutralizing anti-S IgG and T helper cell 1-biased T-cell responses to both S and N that protected the upper and lower respiratory tracts from high titer (1 x 10 TCID) SARS-CoV-2 challenge. Notably, viral replication was inhibited within 24 hours of challenge in both lung and nasal passages, becoming undetectable within 7 days post-challenge.
我们开发了一种双抗原 COVID-19 疫苗,其中包含了经过修饰的 SARS-CoV-2 刺突蛋白(S-Fusion)和病毒核衣壳(N)蛋白的基因,带有增强的 T 细胞刺激结构域(N-ETSD),以增加 MHC 类 II 反应的潜力。疫苗抗原由人类腺病毒血清型 5 平台(hAd5 [E1-,E2b-,E3-])递呈,此前已证明在存在腺病毒免疫的情况下有效。用皮下初免注射和两次口服加强针接种 hAd5 S-Fusion + N-ETSD 疫苗,可引发针对 S 和 N 的中和性抗 S IgG 和 T 辅助细胞 1 偏向性 T 细胞反应,从而保护上呼吸道和下呼吸道免受高滴度(1×10 TCID)SARS-CoV-2 攻击。值得注意的是,在挑战后 24 小时内,肺部和鼻腔中的病毒复制均被抑制,在挑战后 7 天内检测不到。