Rudman Spergel Amanda K, Ananworanich Jintanat, Guo Ruiting, Deng Weiping, Carmona Lizbeth, Schaefers Kristin, Paila Yamuna D, Kandinov Boris, Eger Charles H, Sinkiewicz Melissa, Shao Sarah, Henry Carole, Shaw Christine A
Moderna Inc., Cambridge, MA, USA.
Moderna Biopharma Canada Corporation, Toronto, Ontario, Canada.
Nat Med. 2025 May;31(5):1484-1493. doi: 10.1038/s41591-025-03591-0. Epub 2025 Mar 18.
A multicomponent vaccine targeting several seasonal respiratory pathogens may provide simultaneous protection in a single-injection regimen. We present interim (28 days) findings from a phase 1/2 study of an mRNA-based multicomponent vaccine (mRNA-1083), encoding seasonal influenza and SARS-CoV-2 antigens. Adults (18-79 years) were randomly assigned to receive different compositions of mRNA-1083 at varying dose levels on day 1. The primary study objectives were reactogenicity through 7 days and safety through 28 days postvaccination, and the secondary study objective was immunogenicity against vaccine-matched influenza and SARS-CoV-2 strains at day 29 assessed by hemagglutination inhibition and pseudovirus neutralization assays, respectively. The multicomponent mRNA-1083 vaccine was generally well-tolerated, with most solicited adverse reactions being Grade 1 or 2 in severity. The incidence of unsolicited adverse events was similar across vaccine groups. mRNA-1083 induced immune responses against influenza and SARS-CoV-2 that were, in general, similar to or higher than those achieved with licensed quadrivalent influenza (standard or high dose) and SARS-CoV-2 (bivalent mRNA-1273) vaccines. These data support ongoing phase 3 evaluation of the mRNA-1083 vaccine. ClinicalTrials.gov registration: NCT05827926 .
一种针对多种季节性呼吸道病原体的多组分疫苗可能在单次注射方案中提供同时保护。我们展示了一项1/2期研究的中期(28天)结果,该研究针对一种基于mRNA的多组分疫苗(mRNA-1083),其编码季节性流感和SARS-CoV-2抗原。成人(18 - 79岁)在第1天被随机分配接受不同剂量水平的mRNA-1083不同组成。主要研究目标是接种疫苗后7天内的反应原性和28天内的安全性,次要研究目标是在第29天通过血凝抑制和假病毒中和试验分别评估针对与疫苗匹配的流感和SARS-CoV-2毒株的免疫原性。多组分mRNA-1083疫苗总体耐受性良好,大多数自发报告的不良反应严重程度为1级或2级。各疫苗组中自发不良事件的发生率相似。mRNA-1083诱导的针对流感和SARS-CoV-2的免疫反应总体上与已获许可的四价流感(标准或高剂量)和SARS-CoV-2(二价mRNA-1273)疫苗所达到的免疫反应相似或更高。这些数据支持对mRNA-1083疫苗进行正在进行的3期评估。ClinicalTrials.gov注册号:NCT05827926 。