Jo-Lewis Banga Ndzouboukou , Abdul A. Kamara , Nadeem Ullah , Qing Lei , Xiong-lin Fan
{"title":"针对健康成年人的 SARS-CoV-2 野生型、Omicron BA.1 和 Omicron BA.4/5 疫苗原型、单价适应型和二价疫苗免疫原性的荟萃分析","authors":"Jo-Lewis Banga Ndzouboukou , Abdul A. Kamara , Nadeem Ullah , Qing Lei , Xiong-lin Fan","doi":"10.1016/j.virol.2025.110509","DOIUrl":null,"url":null,"abstract":"<div><div>Although COVID-19 is no longer classified as the first public health emergency, nevertheless, it still presents a serious menace to the health of the global population. Consequently, the development of COVID-19 vaccines possessing an optimal composition that can elicit broad-spectrum neutralizing responses against various SARS-CoV-2 variants is crucial. This meta-analysis aimed to compare the immunogenicity of prototype, monovalent-adapted, and bivalent COVID-19 vaccines against prototype SARS-CoV-2, Omicron BA.1 variant, and Omicron BA.4/5 subvariant in healthy adults. We utilized 4 medical databases to retrieve original studies and employed the fixed effect model to estimate pooled neutralization titers. A total of 12 studies concerning 4581 subjects were included in the meta-analysis. We found that participants who received prototype, monovalent-adapted, and bivalent vaccines as a second booster significantly developed neutralizing antibody (nAb) titers against prototype SARS-CoV-2, Omicron BA.1 variant, and Omicron BA.4/5 subvariant, with monovalent-adapted and bivalent vaccines exhibiting a higher increment. Furthermore, the bivalent(Prototype/Omicron BA.1) recombinant protein vaccine exhibited the highest increment in neutralization titers(MD = 1.95; 95 %CI:0.78–3.12; <em>p</em> < 0.01) against the prototype SARS-CoV-2 and Omicron BA.4/5 subvariant compared to the other vaccine regimens. Interestingly, only individuals who received the monovalent (Omicron BA.1)-adapted mRNA vaccine as a second booster showed the highest increase in neutralization titers (MD:1.37; 95 %CI:0.50–2.24; <em>p</em> < 0.01) against the Omicron BA.1 variant compared to the other vaccine regimens. These findings showed that bivalent recombinant protein vaccines seem more immunogenic than bivalent mRNA vaccines, and bivalent vaccines might not be superior immunogens for induced strong protective immune responses compared to monovalent-adapted vaccines.</div></div>","PeriodicalId":23666,"journal":{"name":"Virology","volume":"606 ","pages":"Article 110509"},"PeriodicalIF":2.8000,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A meta-analysis on the immunogenicity of prototype, monovalent-adapted and bivalent vaccines against SARS-CoV-2 wildtype, Omicron BA.1 and Omicron BA.4/5 in healthy adults\",\"authors\":\"Jo-Lewis Banga Ndzouboukou , Abdul A. Kamara , Nadeem Ullah , Qing Lei , Xiong-lin Fan\",\"doi\":\"10.1016/j.virol.2025.110509\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Although COVID-19 is no longer classified as the first public health emergency, nevertheless, it still presents a serious menace to the health of the global population. Consequently, the development of COVID-19 vaccines possessing an optimal composition that can elicit broad-spectrum neutralizing responses against various SARS-CoV-2 variants is crucial. This meta-analysis aimed to compare the immunogenicity of prototype, monovalent-adapted, and bivalent COVID-19 vaccines against prototype SARS-CoV-2, Omicron BA.1 variant, and Omicron BA.4/5 subvariant in healthy adults. We utilized 4 medical databases to retrieve original studies and employed the fixed effect model to estimate pooled neutralization titers. A total of 12 studies concerning 4581 subjects were included in the meta-analysis. We found that participants who received prototype, monovalent-adapted, and bivalent vaccines as a second booster significantly developed neutralizing antibody (nAb) titers against prototype SARS-CoV-2, Omicron BA.1 variant, and Omicron BA.4/5 subvariant, with monovalent-adapted and bivalent vaccines exhibiting a higher increment. Furthermore, the bivalent(Prototype/Omicron BA.1) recombinant protein vaccine exhibited the highest increment in neutralization titers(MD = 1.95; 95 %CI:0.78–3.12; <em>p</em> < 0.01) against the prototype SARS-CoV-2 and Omicron BA.4/5 subvariant compared to the other vaccine regimens. Interestingly, only individuals who received the monovalent (Omicron BA.1)-adapted mRNA vaccine as a second booster showed the highest increase in neutralization titers (MD:1.37; 95 %CI:0.50–2.24; <em>p</em> < 0.01) against the Omicron BA.1 variant compared to the other vaccine regimens. These findings showed that bivalent recombinant protein vaccines seem more immunogenic than bivalent mRNA vaccines, and bivalent vaccines might not be superior immunogens for induced strong protective immune responses compared to monovalent-adapted vaccines.</div></div>\",\"PeriodicalId\":23666,\"journal\":{\"name\":\"Virology\",\"volume\":\"606 \",\"pages\":\"Article 110509\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-03-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Virology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0042682225001229\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"VIROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0042682225001229","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"VIROLOGY","Score":null,"Total":0}
A meta-analysis on the immunogenicity of prototype, monovalent-adapted and bivalent vaccines against SARS-CoV-2 wildtype, Omicron BA.1 and Omicron BA.4/5 in healthy adults
Although COVID-19 is no longer classified as the first public health emergency, nevertheless, it still presents a serious menace to the health of the global population. Consequently, the development of COVID-19 vaccines possessing an optimal composition that can elicit broad-spectrum neutralizing responses against various SARS-CoV-2 variants is crucial. This meta-analysis aimed to compare the immunogenicity of prototype, monovalent-adapted, and bivalent COVID-19 vaccines against prototype SARS-CoV-2, Omicron BA.1 variant, and Omicron BA.4/5 subvariant in healthy adults. We utilized 4 medical databases to retrieve original studies and employed the fixed effect model to estimate pooled neutralization titers. A total of 12 studies concerning 4581 subjects were included in the meta-analysis. We found that participants who received prototype, monovalent-adapted, and bivalent vaccines as a second booster significantly developed neutralizing antibody (nAb) titers against prototype SARS-CoV-2, Omicron BA.1 variant, and Omicron BA.4/5 subvariant, with monovalent-adapted and bivalent vaccines exhibiting a higher increment. Furthermore, the bivalent(Prototype/Omicron BA.1) recombinant protein vaccine exhibited the highest increment in neutralization titers(MD = 1.95; 95 %CI:0.78–3.12; p < 0.01) against the prototype SARS-CoV-2 and Omicron BA.4/5 subvariant compared to the other vaccine regimens. Interestingly, only individuals who received the monovalent (Omicron BA.1)-adapted mRNA vaccine as a second booster showed the highest increase in neutralization titers (MD:1.37; 95 %CI:0.50–2.24; p < 0.01) against the Omicron BA.1 variant compared to the other vaccine regimens. These findings showed that bivalent recombinant protein vaccines seem more immunogenic than bivalent mRNA vaccines, and bivalent vaccines might not be superior immunogens for induced strong protective immune responses compared to monovalent-adapted vaccines.
期刊介绍:
Launched in 1955, Virology is a broad and inclusive journal that welcomes submissions on all aspects of virology including plant, animal, microbial and human viruses. The journal publishes basic research as well as pre-clinical and clinical studies of vaccines, anti-viral drugs and their development, anti-viral therapies, and computational studies of virus infections. Any submission that is of broad interest to the community of virologists/vaccinologists and reporting scientifically accurate and valuable research will be considered for publication, including negative findings and multidisciplinary work.Virology is open to reviews, research manuscripts, short communication, registered reports as well as follow-up manuscripts.