» Articles » PMID: 36851745

Dynamics of SARS-CoV-2 VOC Neutralization and Novel MAb Reveal Protection Against Omicron

Abstract

New variants of SARS-CoV-2 continue to emerge and evade immunity. We isolated SARS-CoV-2 temporally across the pandemic starting with the first emergence of the virus in the western hemisphere and evaluated the immune escape among variants. A clinic-to-lab viral isolation and characterization pipeline was established to rapidly isolate, sequence, and characterize SARS-CoV-2 variants. A virus neutralization assay was applied to quantitate humoral immunity from infection and/or vaccination. A panel of novel monoclonal antibodies was evaluated for antiviral efficacy. We directly compared all variants, showing that convalescence greater than 5 months post-symptom onset from ancestral virus provides little protection against SARS-CoV-2 variants. Vaccination enhances immunity against viral variants, except for Omicron BA.1, while a three-dose vaccine regimen provides over 50-fold enhanced protection against Omicron BA.1 compared to a two-dose. A novel Mab neutralizes Omicron BA.1 and BA.2 variants better than the clinically approved Mabs, although neither can neutralize Omicron BA.4 or BA.5. Thus, the need remains for continued vaccination-booster efforts, with innovation for vaccine and Mab improvement for broadly neutralizing activity. The usefulness of specific Mab applications links with the window of clinical opportunity when a cognate viral variant is present in the infected population.

Citing Articles

Dynamics of spike-specific neutralizing antibodies across five-year emerging SARS-CoV-2 variants of concern reveal conserved epitopes that protect against severe COVID-19.

Zayou L, Prakash S, Vahed H, Dhanushkodi N, Quadiri A, Belmouden A Front Immunol. 2025; 16:1503954.

PMID: 40040708 PMC: 11876060. DOI: 10.3389/fimmu.2025.1503954.


Dynamics of Spike-Specific Neutralizing Antibodies Across Five-Year Emerging SARS-CoV-2 Variants of Concern Reveal Conserved Epitopes that Protect Against Severe COVID-19.

Zayou L, Prakash S, Vahed H, Dhanushkodi N, Quadiri A, Belmouden A bioRxiv. 2024; .

PMID: 39386567 PMC: 11463540. DOI: 10.1101/2024.09.22.614369.


Screening Peptide Drug Candidates To Neutralize Whole Viral Agents: A Case Study with Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2).

Ozcelik C, Araz C, Yilmaz O, Gulyuz S, Ozdamar P, Salmanli E ACS Pharmacol Transl Sci. 2024; 7(4):1032-1042.

PMID: 38633598 PMC: 11020059. DOI: 10.1021/acsptsci.3c00317.


Innate immunity and interferon in SARS-CoV-2 infection outcome.

Savan R, Gale Jr M Immunity. 2023; 56(7):1443-1450.

PMID: 37437537 PMC: 10361255. DOI: 10.1016/j.immuni.2023.06.018.

References
1.
Kumar S, Stecher G, Li M, Knyaz C, Tamura K . MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms. Mol Biol Evol. 2018; 35(6):1547-1549. PMC: 5967553. DOI: 10.1093/molbev/msy096. View

2.
Garcia-Beltran W, Lam E, St Denis K, Nitido A, Garcia Z, Hauser B . Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity. Cell. 2021; 184(9):2372-2383.e9. PMC: 7953441. DOI: 10.1016/j.cell.2021.03.013. View

3.
Perchetti G, Zhu H, Mills M, Shrestha L, Wagner C, Bakhash S . Specific allelic discrimination of N501Y and other SARS-CoV-2 mutations by ddPCR detects B.1.1.7 lineage in Washington State. J Med Virol. 2021; 93(10):5931-5941. PMC: 8427099. DOI: 10.1002/jmv.27155. View

4.
Bowen J, Addetia A, Dang H, Stewart C, Brown J, Sharkey W . Omicron spike function and neutralizing activity elicited by a comprehensive panel of vaccines. Science. 2022; 377(6608):890-894. PMC: 9348749. DOI: 10.1126/science.abq0203. View

5.
Iketani S, Liu L, Guo Y, Liu L, Chan J, Huang Y . Antibody evasion properties of SARS-CoV-2 Omicron sublineages. Nature. 2022; 604(7906):553-556. PMC: 9021018. DOI: 10.1038/s41586-022-04594-4. View