In a recent study, researchers in the United States assessed the impact of the bivalent messenger ribonucleic acid (mRNA) severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine on the antibody-mediated neutralization of the SARS-CoV-2 Omicron lineages.
Early SARS-CoV-2 Omicron lineage variants have mutated, resulting in divergent lineages that drove the 2022 coronavirus disease 2019 (COVID-19) pandemic. As a result, the U.S. Food and Drug Administration (FDA) authorized bivalent mRNA vaccines designed to widen protection against current and future variants in August 2022, and the U.S. Centers for Disease Control and Prevention (CDC) recommended their use in September 2022. However, the effect of bivalent vaccination on the production of neutralizing antibodies against SARS-CoV-2 homologous Omicron BA.4/BA.5 viruses and emerging heterologous viruses needs extensive evaluation.
Study
In the present study, the researchers examined the neutralization activity of serum samples obtained after the third or fourth COVID-19 vaccination dose against ten prevalent or recent SARS-CoV-2 Omicron lineage viruses, including BA.2.75, BA.2.75.2, BA.1, BA.2, BA.5, BQ.1, BQ.1.1, XBB, XBB.1, and BN.1.
The team obtained serum samples from vaccine recipients two to six weeks after being vaccinated with the third dose or two to seven weeks after vaccination with the fourth dosage of a bivalent booster mRNA vaccine. Using Meso Scale Discovery (MSD) assays, the total immunoglobulin (Ig)-G antibody response was compared between post-third vaccine dose sera and post-fourth vaccine dose sera in response to representative spike proteins associated with the progenitor index virus (614D) and SARS-CoV-2 Alpha, Delta, Beta, and Omicron BA.1, BA.5, BA.2, and BA.2.75 lineages.
To assess the neutralizing effectiveness of post-third vaccination and post-bivalent vaccination dosage sera against major Omicron lineage viruses, the team created lineage-specific spike mutations corresponding to the Omicron BA.1 spike background, giving rise to reporter viruses related to 10 Omicron lineage viruses. To precisely investigate the impact of distinct spike domains in antibody evasion, the lineages BA.1, BA.2, BA.4, and BA.5 were selected, and their receptor-binding domain (RBD) and non-RBD spike variants were isolated. Pooled post-second dose sera and pooled post-third dosage sera were used to examine all the viruses.
Findings
After the third vaccine dosage, the anti-spike binding activity decreased minimally for SARS-CoV-2 Alpha, Beta, and Delta, with fold decreases of 1.2, 1.7, and 1.4 concerning the 614D standard, respectively. With fold-change reductions of 4.2, 3.8, 3.7, and 5.6, respectively, BA.1, BA.5, BA.2, and BA.2.75 exhibited the most significant alterations. Compared to the post-third dose serum samples, the post-bivalent vaccination serum had slightly greater activity against all the viral spike antigens. In the MSD test, however, the breadth/specificity of these two sera was comparable, as the fold changes with respect to the 614D spike among B.A.1, BA.5, BA.2, and BA.2.75 observed post-third dose and post-bivalent sera were comparable.
The sera from the third dosage exhibited significant neutralizing activity in response to the 614D reference virus, moderate activity in response to the BA.1, BA.2, BA.5, and BA.2.75 strains, and poor activity against the BA.2.75.2, BQ.1, BQ.1.1, BN.1, XBB, and XBB.1 strains. Compared to the 614D nAb titers, the BA.1, BA.5, BA.2, and BA.2.75 nAb titers were reduced by five, eight, 20, and 12 times, respectively. Compared to 614D, the titers of the BA.2.75-2 and BN.1 lineages fell by 127 and 64 times, respectively. Furthermore, in comparison to 614D, the titers of BQ.1 and BQ.1.1 lineages declined by 190 and 288 times, respectively. XBB and XBB.1 had the most significant degree of escape, with 324 and 371 times reductions in nAb titers compared to 614D.
With respect to the post-third vaccine dose sera, the neutralizing activity noted in response to the 614D reference rose by 1.4 times in the post-bivalent vaccination sera; however, it increased considerably against other Omicron lineages. Post-bivalent vaccination sera were 7.1 times more effective at BA.5 neutralization and 2.9 to 5.1 times more effective at the neutralization of heterologous antigens like BA.1, BA.2, BA.2.75, BA.2.75.2, and BN.1 in comparison to the post-third vaccine dose sera. The more considerable rise of BA.5 lineage viruses compared to BA.1/BA.2 lineage viruses suggested that the bivalent mRNA vaccination induced BA.5 lineage-specific antibodies.
In comparison to the 614D virus, post-second dose and post-third dose titers reductions for the BA.1 were 45- and eight-fold, BA.2 were 38- and 11-fold, BA.5 were 29- and 10-fold and XBB.1 were over 192- and 289-fold. Viruses bearing only RBD mutations were related with post-second and post-third dose titer reductions of one- and one-fold for BA.1, three- and four-fold for BA.2, seven- and eight-fold for BA.5, and 38- and 17-fold for XBB.1. Removing the RBD mutations restored the virus neutralizing titers to values close to 614D in both post-second and post-third serum samples.
Conclusion
The study findings showed that the neutralizing titers improved by 7.1-fold against SARS-CoV-2 Omicron BA.5 lineage and 12-fold against the BQ.1 and BQ.1.1 lineages between the post-third dose monovalent and post-fourth dose bivalent vaccine sera. This indicated that the improved neutralizing titers caused higher vaccine efficiency after bivalent vaccination. Despite the fact that the variables of protection against SARS-CoV-2 must be defined in total, they may be explored further based on additional data from the investigations of the efficacy of the COVID-19 vaccine.
Source:
https://www.news-medical.net/news/20230111/Bivalent-boosters-tested-against-all-SARS-CoV-2-Omicron-lineages.aspx