Trans amplifying mRNA vaccine expressing consensus spike elicits broad neutralization of SARS CoV 2 variants.

IF 6.9 1区 医学 Q1 IMMUNOLOGY
Abhinay Gontu, Sougat Misra, Shubhada K Chothe, Santhamani Ramasamy, Padmaja Jakka, Maurice Byukusenge, Lindsey C LaBella, Meera Surendran Nair, Bhushan M Jayarao, Marco Archetti, Ruth H Nissly, Suresh V Kuchipudi
{"title":"Trans amplifying mRNA vaccine expressing consensus spike elicits broad neutralization of SARS CoV 2 variants.","authors":"Abhinay Gontu, Sougat Misra, Shubhada K Chothe, Santhamani Ramasamy, Padmaja Jakka, Maurice Byukusenge, Lindsey C LaBella, Meera Surendran Nair, Bhushan M Jayarao, Marco Archetti, Ruth H Nissly, Suresh V Kuchipudi","doi":"10.1038/s41541-025-01166-1","DOIUrl":null,"url":null,"abstract":"<p><p>SARS-CoV-2 continues to evolve and evade vaccine immunity necessitating vaccines that offer broad protection across variants. Conventional mRNA vaccines face cost and scalability challenges, prompting the exploration of alternative platforms like trans-amplifying (TA) mRNA that offer advantages in safety, manufacturability, and antigen dose optimization. Using consensus sequence of immunodominant antigens is a promising antigen design strategy for board cross-protection. Combining these two features, we designed and evaluated a TA mRNA vaccine encoding a consensus spike protein from SARS-CoV-2. Mice receiving the TA mRNA vaccine produced neutralizing antibody levels comparable to a conventional mRNA vaccine using 40 times less antigen mRNA. In hACE2 transgenic mice challenged with the Omicron BA.1 variant, the TA mRNA vaccine reduced lung viral titers by over 10-fold and induced broadly cross-neutralizing antibodies against multiple variants. These findings highlight the potential of TA mRNA vaccines with consensus antigen design, to improve efficacy and adaptability against SARS-CoV-2 variants.</p>","PeriodicalId":19335,"journal":{"name":"NPJ Vaccines","volume":"10 1","pages":"110"},"PeriodicalIF":6.9000,"publicationDate":"2025-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12134344/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NPJ Vaccines","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41541-025-01166-1","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

SARS-CoV-2 continues to evolve and evade vaccine immunity necessitating vaccines that offer broad protection across variants. Conventional mRNA vaccines face cost and scalability challenges, prompting the exploration of alternative platforms like trans-amplifying (TA) mRNA that offer advantages in safety, manufacturability, and antigen dose optimization. Using consensus sequence of immunodominant antigens is a promising antigen design strategy for board cross-protection. Combining these two features, we designed and evaluated a TA mRNA vaccine encoding a consensus spike protein from SARS-CoV-2. Mice receiving the TA mRNA vaccine produced neutralizing antibody levels comparable to a conventional mRNA vaccine using 40 times less antigen mRNA. In hACE2 transgenic mice challenged with the Omicron BA.1 variant, the TA mRNA vaccine reduced lung viral titers by over 10-fold and induced broadly cross-neutralizing antibodies against multiple variants. These findings highlight the potential of TA mRNA vaccines with consensus antigen design, to improve efficacy and adaptability against SARS-CoV-2 variants.

表达共识尖峰的反式扩增mRNA疫苗可广泛中和SARS冠状病毒2变体。
SARS-CoV-2继续进化并逃避疫苗免疫,这就需要疫苗在不同变体之间提供广泛的保护。传统的mRNA疫苗面临成本和可扩展性方面的挑战,促使人们探索诸如反式扩增(TA) mRNA等替代平台,这些平台在安全性、可制造性和抗原剂量优化方面具有优势。采用一致的免疫优势抗原序列是一种很有前途的抗原设计策略。结合这两个特征,我们设计并评估了一种编码SARS-CoV-2共识刺突蛋白的TA mRNA疫苗。接受TA mRNA疫苗的小鼠产生的中和抗体水平与使用抗原mRNA少40倍的传统mRNA疫苗相当。在使用Omicron BA.1变异的hACE2转基因小鼠中,TA mRNA疫苗将肺病毒滴度降低了10倍以上,并诱导了针对多种变异的广泛交叉中和抗体。这些发现突出了具有一致抗原设计的TA mRNA疫苗在提高针对SARS-CoV-2变体的效力和适应性方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
NPJ Vaccines
NPJ Vaccines Immunology and Microbiology-Immunology
CiteScore
11.90
自引率
4.30%
发文量
146
审稿时长
11 weeks
期刊介绍: Online-only and open access, npj Vaccines is dedicated to highlighting the most important scientific advances in vaccine research and development.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信