Preclinical Characterization of the Omicron XBB.1.5-Adapted BNT162b2 COVID-19 Vaccine

Kayvon Modjarrad,Ye Che, Wei Chen,Huixian Wu, Carla I Cadima,Alexander Muik,Mohan S Maddur,Kristin R Tompkins, Lyndsey T Martinez, Hui Cai, Minah Hong, Sonia Mensah, Brittney Cumbia, Larissa Falcao, Jeanne S Chang, Kimberly F Fennell, Kevin Hyunh, Thomas J McLellan,Parag Sahasrabudhe, Wei Chen, Michael Cerswell, Miguel A Garcia, Shilong Li, Rahul Sharma, Weiqiang Li, Kristianne Dizon, Stacy Duarte, Frank Gillett, Rachel Smith, Deanne M Illenberger, Kari E Sweeney,Annette B Vogel,Annaliesa S Anderson,Ugur Sahin,Kena Swanson

biorxiv(2023)

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摘要
As SARS-CoV-2 continues to evolve, increasing in its potential for greater transmissibility and immune escape, updated vaccines are needed to boost adaptive immunity to protect against COVID-19 caused by circulating strains. Here, we report features of the monovalent Omicron XBB.1.5-adapted BNT162b2 vaccine, which contains the same mRNA backbone as the original BNT162b2 vaccine, modified by the incorporation of XBB.1.5-specific sequence changes in the encoded prefusion-stabilized SARS-CoV-2 spike protein (S(P2)). Biophysical characterization of Omicron XBB.1.5 S(P2) demonstrated that it maintains a prefusion conformation that adopts a flexible and predominantly open one-RBD-up state, with high affinity binding to the human ACE-2 receptor. When administered as a 4th dose in BNT162b2-experienced mice, the monovalent Omicron XBB.1.5 vaccine elicited substantially higher serum neutralizing titers against pseudotyped viruses of Omicron XBB.1.5, XBB.1.16, XBB.1.16.1, XBB.2.3, EG.5.1 and HV.1 sublineages and the phylogenetically distant BA.2.86 lineage than the bivalent Wild Type + Omicron BA.4/5 vaccine. Similar trends were observed against Omicron XBB sublineage pseudoviruses when the vaccine was administered as a 2-dose primary series in naive mice. Strong S-specific Th1 CD4+ and IFN[&gamma]+ CD8+ T cell responses were also observed. These findings, together with prior experience with variant-adapted vaccine responses in preclinical and clinical studies, suggest that the monovalent Omicron XBB.1.5-adapted BNT162b2 vaccine is anticipated to confer protective immunity against dominant SARS-CoV-2 strains. ### Competing Interest Statement All authors are employees of Pfizer or BioNTech and may, therefore, be respective shareholders. Pfizer and BioNTech participated in the design, analysis and interpretation of the data as well as the writing of this report and the decision to publish. KM, YC, AM, HC, AV, UŞ and KAS are inventors on patents and patent applications related to the COVID-19 vaccine. AM, AV and UŞ are inventors on patents and patent applications related to RNA technology.
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