A Bivalent Omicron-Containing Booster Vaccine against Covid-19

二价(发动机) 医学 助推器(火箭) 病毒学 免疫原性 信使核糖核酸 反应性 增强剂量 免疫学 化学 抗体 病毒 基因 物理 效价 生物化学 金属 有机化学 天文
作者
Spyros Chalkias,Charles Harper,Keith Vrbicky,Stephen R. Walsh,Brandon Essink,Adam Brosz,Nichole McGhee,Joanne E. Tomassini,Xing Chen,Ying Chang,Andrea Sutherland,David C. Montefiori,Bethany Girard,Darin K. Edwards,Jing Feng,Haiyu Zhou,Lindsey R. Baden,Jacqueline M. Miller,Rituparna Das
出处
期刊:The New England Journal of Medicine [New England Journal of Medicine]
卷期号:387 (14): 1279-1291 被引量:571
标识
DOI:10.1056/nejmoa2208343
摘要

The safety and immunogenicity of the bivalent omicron-containing mRNA-1273.214 booster vaccine are not known.In this ongoing, phase 2-3 study, we compared the 50-μg bivalent vaccine mRNA-1273.214 (25 μg each of ancestral Wuhan-Hu-1 and omicron B.1.1.529 [BA.1] spike messenger RNAs) with the previously authorized 50-μg mRNA-1273 booster. We administered mRNA-1273.214 or mRNA-1273 as a second booster in adults who had previously received a two-dose (100-μg) primary series and first booster (50-μg) dose of mRNA-1273 (≥3 months earlier). The primary objectives were to assess the safety, reactogenicity, and immunogenicity of mRNA-1273.214 at 28 days after the booster dose.Interim results are presented. Sequential groups of participants received 50 μg of mRNA-1273.214 (437 participants) or mRNA-1273 (377 participants) as a second booster dose. The median time between the first and second boosters was similar for mRNA-1273.214 (136 days) and mRNA-1273 (134 days). In participants with no previous severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, the geometric mean titers of neutralizing antibodies against the omicron BA.1 variant were 2372.4 (95% confidence interval [CI], 2070.6 to 2718.2) after receipt of the mRNA-1273.214 booster and 1473.5 (95% CI, 1270.8 to 1708.4) after receipt of the mRNA-1273 booster. In addition, 50-μg mRNA-1273.214 and 50-μg mRNA-1273 elicited geometric mean titers of 727.4 (95% CI, 632.8 to 836.1) and 492.1 (95% CI, 431.1 to 561.9), respectively, against omicron BA.4 and BA.5 (BA.4/5), and the mRNA-1273.214 booster also elicited higher binding antibody responses against multiple other variants (alpha, beta, gamma, and delta) than the mRNA-1273 booster. Safety and reactogenicity were similar with the two booster vaccines. Vaccine effectiveness was not assessed in this study; in an exploratory analysis, SARS-CoV-2 infection occurred in 11 participants after the mRNA-1273.214 booster and in 9 participants after the mRNA-1273 booster.The bivalent omicron-containing vaccine mRNA-1273.214 elicited neutralizing antibody responses against omicron that were superior to those with mRNA-1273, without evident safety concerns. (Funded by Moderna; ClinicalTrials.gov number, NCT04927065.).
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