Academic Journal

Multivalent mRNA Vaccine Elicits Broad Protection against SARS-CoV-2 Variants of Concern

التفاصيل البيبلوغرافية
العنوان: Multivalent mRNA Vaccine Elicits Broad Protection against SARS-CoV-2 Variants of Concern
المؤلفون: Monika Kumari, Kang-Hao Liang, Shih-Chieh Su, Hsiu-Ting Lin, Yu-Feng Lu, Ming-Jane Wu, Wan-Yu Chen, Han-Chung Wu
المصدر: Vaccines, Vol 12, Iss 7, p 714 (2024)
بيانات النشر: MDPI AG, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
مصطلحات موضوعية: SARS-CoV-2, variants of concern, multivalent mRNA vaccines, vaccine efficacy, Medicine
الوصف: SARS-CoV-2 new waves are primarily caused by changes to the spike protein (S), which can substantially decrease the efficacy of vaccines. Therefore, we tested several multivalent mRNA-LNP vaccines, targeting the full-length S proteins of different variants, and identified an optimal combination for protection against VOCs in BALB/c mice. The tested formulations included trivalent (WT + BA.5 + XBB.1.5), pentavalent (WT + BA.5 + XBB.1.5 + BQ.1.1 + CH.1.1), and octavalent (WT + BA.5 + XBB.1.5 + BQ.1.1 + CH.1.1 + Alpha + Delta + BA.2) vaccines. Among these multivalent vaccines, the pentavalent vaccine showed superior protection for almost all tested variants. Despite this, each multivalent vaccine elicited greater broad-spectrum neutralizing antibodies than the previously evaluated bivalent vaccine (WT + BA.5). Subsequently, we redesigned the multivalent vaccine to efficiently generate neutralizing antibodies against recent VOCs, including EG.5.1. Immunization with the redesigned pentavalent vaccine (WT + EG.5.1 + XBB.1.16 + Delta + BA.5) showed moderate levels of protection against recent Omicron VOCs. Results suggest that the neutralization activity of multivalent vaccines is better than those of the tested bivalent vaccines against WT + BA.5 and WT + EG.5.1. Moreover, the pentavalent vaccine we developed may be highly useful for neutralizing new Omicron VOCs.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2076-393X
Relation: https://www.mdpi.com/2076-393X/12/7/714; https://doaj.org/toc/2076-393X
DOI: 10.3390/vaccines12070714
URL الوصول: https://doaj.org/article/065a807d43ca4f63bb9b8eec1855c9e7
رقم الانضمام: edsdoj.065a807d43ca4f63bb9b8eec1855c9e7
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2076393X
DOI:10.3390/vaccines12070714