Frontiers in ImmunologyImmunologyPeer-reviewed journal article
Addressing SARS-CoV-2 Evolution: Neutralization of Emerging Variants of Concern by the AVX/COVID-12 'Patria' Vaccine Based on HexaPro-S Ancestral Wuhan Spike or Its Updated BA.2.75.2 Version
Gregorio Carballo‐UicabiD, Gabriela Mellado‐SáncheziD, Edith González‐GonzáleziD, Juana Salinas-TrujanoiD, Ivette Mendoza-SalazariD, Karina López-OlveraiD, Keyla Gómez-CastellanoiD, Ma. Isabel SalazariD, Jesús Miguel Torres-FloresiD, Héctor Elías Chagoya-CortésiD, Georgina Paz-De la RosaiD, Ignacio MenaiD, Oscar Rojas-MartíneziD, Jesús Horacio Lara PuenteiD, Gustavo Peralta-SáncheziD, David Sarfati-MizrahiiD, Alejandro Torres-FloresiD, Weina SuniD, Florian KrammeriD, Adolfo García‐SastreiD, Peter PaleseiD, Constantino III Roberto López-MacíasiD, Bernardo Lozano-DubernardiD, Sonia Mayra Pérez‐TapiaiD, Juan Carlos AlmagroiD
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains a global health challenge, causing severe morbidity and mortality, particularly in vulnerable groups such as the elderly, immunocompromised individuals, and those with comorbidities. In low- and middle-income countries (LMICs), vaccine access is hindered by high costs and inequitable distribution. To tackle these issues, Mexico developed the AVX/COVID-12 (V-Wu) vaccine, a recombinant Newcastle disease virus (NDV)-based platform expressing a stabilized ancestral Wuhan spike protein (HexaPro-S). Locally manufactured after rigorous testing and regulatory approval, V-Wu aims to enhance self-sufficiency and equity in immunization. This study evaluates an updated vaccine version, AVX/COVID-12 (V-BA), designed to combat Omicron subvariants by expressing the HexaPro-S protein of BA.2.75.2. Both vaccines were administered intramuscularly in K18-hACE2 transgenic and BALB/c mouse models using a prime-boost regimen. Immunogenicity was analyzed by measuring antibodies against Omicron S proteins BA.2.75.2 and XBB.1.5, as well as neutralizing antibodies against Wuhan, BA.1, XBB.1.16, and JN.1 variants. Both vaccines were safe, eliciting robust antibody responses against Omicron S proteins and neutralizing antibodies against multiple emerging SARS-CoV-2 variants of concern (VOCs). V-BA demonstrated superior protection against current Omicron variants, while V-Wu offered broader coverage, including the ancestral Wuhan strain and emerging variants like JN.1. These findings underscore the adaptability of NDV-based platforms in addressing the evolving SARS-CoV-2 landscape and reaffirm the ongoing utility of the ancestral Patria vaccine. Together, they demonstrate the potential of these platforms to drive the development of next-generation vaccines tailored to emerging viral threats, contributing to global health equity.
- organism: mouse
- assay: proteomics
- research focus: host-pathogen & immune response
- approach: experimental assay
- Citations
- 3
- FWCI
- 2.29
- Field percentile
- top 14%
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