Optimization of Non-Coding Regions Improves Protective Efficacy of an mRNA SARS-CoV-2 Vaccine in Nonhuman Primates
Gebre, M.; Rauch, S.; Roth, N.; Yu, J.; Chandrashekar, A.; Mercado, N.; He, X.; Liu, J.; McMahan, K.; Martinot, A.; Giffin, T.; Hope, D.; Patel, S.; Sellers, D.; Sanborn, O.; Barrett, J.; Liu, X.; Cole, A.; Pessaint, L.; Valentin, D.; Flinchbaugh, Z.; Yalley-Ogunro, J.; Muench, J.; Brown, R.; Cook, A.; Teow, E.; Andersen, H.; Lewis, M. G.; Mueller, S.; Petsch, B.; Barouch, D. H.
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The CVnCoV (CureVac) mRNA vaccine for SARS-CoV-2 has recently been evaluated in a phase 2b/3 efficacy trial in humans. CV2CoV is a second-generation mRNA vaccine with optimized non-coding regions and enhanced antigen expression. Here we report a head-to-head study of the immunogenicity and protective efficacy of CVnCoV and CV2CoV in nonhuman primates. We immunized 18 cynomolgus macaques with two doses of 12 ug of lipid nanoparticle formulated CVnCoV, CV2CoV, or sham (N=6/group). CV2CoV induced substantially higher binding and neutralizing antibodies, memory B cell responses, and T cell responses as compared with CVnCoV. CV2CoV also induced more potent neutralizing antibody responses against SARS-CoV-2 variants, including B.1.351 (beta), B.1.617.2 (delta), and C.37 (lambda). While CVnCoV provided partial protection against SARS-CoV-2 challenge, CV2CoV afforded robust protection with markedly lower viral loads in the upper and lower respiratory tract. Antibody responses correlated with protective efficacy. These data demonstrate that optimization of non-coding regions can greatly improve the immunogenicity and protective efficacy of an mRNA SARS-CoV-2 vaccine in nonhuman primates.
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