Ying Baoling, Scheaffer Suzanne M, Whitener Bradley, Liang Chieh-Yu, Dmytrenko Oleksandr, Mackin Samantha, Wu Kai, Lee Diana, Avena Laura E, Chong Zhenlu, Case James Brett, Ma LingZhi, Kim Thu, Sein Caralyn, Woods Angela, Berrueta Daniela Montes, Carfi Andrea, Elbashir Sayda M, Edwards Darin K, Thackray Larissa B, Diamond Michael S
Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO, USA.
bioRxiv. 2022 Feb 9:2022.02.07.479419. doi: 10.1101/2022.02.07.479419.
The B.1.1.529 Omicron variant jeopardizes vaccines designed with early pandemic spike antigens. Here, we evaluated in mice the protective activity of the Moderna mRNA-1273 vaccine against B.1.1.529 before or after boosting with preclinical mRNA-1273 or mRNA-1273.529, an Omicron-matched vaccine. Whereas two doses of mRNA-1273 vaccine induced high levels of serum neutralizing antibodies against historical WA1/2020 strains, levels were lower against B.1.1.529 and associated with infection and inflammation in the lung. A primary vaccination series with mRNA-1273.529 potently neutralized B.1.1.529 but showed limited inhibition of historical or other SARS-CoV-2 variants. However, boosting with mRNA-1273 or mRNA-1273.529 vaccines increased serum neutralizing titers and protection against B.1.1.529 infection. Nonetheless, the levels of inhibitory antibodies were higher, and viral burden and cytokines in the lung were slightly lower in mice given the Omicron-matched mRNA booster. Thus, in mice, boosting with mRNA-1273 or mRNA-1273.529 enhances protection against B.1.1.529 infection with limited differences in efficacy measured.
B.1.1.529奥密克戎变种对基于早期大流行毒株刺突抗原设计的疫苗构成了威胁。在此,我们在小鼠中评估了Moderna的mRNA-1273疫苗在使用临床前mRNA-1273或奥密克戎匹配疫苗mRNA-1273.529加强免疫之前或之后对B.1.1.529的保护活性。两剂mRNA-1273疫苗可诱导产生高水平的针对历史毒株WA1/2020的血清中和抗体,但针对B.1.1.529的抗体水平较低,且与肺部感染和炎症相关。用mRNA-1273.529进行的初次疫苗接种系列能有效中和B.1.1.529,但对历史毒株或其他SARS-CoV-2变种的抑制作用有限。然而,用mRNA-1273或mRNA-1273.529疫苗加强免疫可提高血清中和滴度,并增强对B.1.1.529感染的保护作用。尽管如此,接受奥密克戎匹配的mRNA加强针的小鼠体内,抑制性抗体水平更高,肺部病毒载量和细胞因子水平略低。因此,在小鼠中,用mRNA-1273或mRNA-1273.529加强免疫可增强对B.1.1.529感染的保护作用,且在疗效测量上差异有限。