Key result
Novel multivariant surrogate-virus neutralization tests strongly correlate with live-virus tests for assessing variant-specific antibodies.
Why the study?
Assessing variant-specific neutralizing antibody profiles after bivalent vaccination typically requires laborious live-virus neutralization tests, prompting evaluation of a novel multivariant surrogate-virus neutralization test.
Does a multivariant surrogate-virus neutralization test correlate with live-virus neutralization tests in assessing neutralizing activity against SARS-CoV-2 variants?
Observational (n=95)
Does a multivariant surrogate-virus neutralization test correlate with live-virus neutralization tests in assessing neutralizing activity against SARS-CoV-2 variants?
A novel multivariant surrogate-virus neutralization test can reliably detect variant-specific neutralizing antibodies following booster vaccination, correlating well with laborious live-virus tests.
Answers are grounded in this paper and cite their sources.
May enable scalable variant neutralization monitoring post-vaccination; leaves open prospective validation before clinical adoption.
The capability of antibodies to neutralize different SARS-CoV-2 variants varies among individuals depending on the previous exposure to wild-type or Omicron-specific immunogens by mono- or bivalent vaccinations or infections. Such profiles of neutralizing antibodies (nAbs) usually have to be assessed via laborious live-virus neutralization tests (NTs). We therefore analyzed whether a novel multivariant surrogate-virus neutralization test (sVNT) (adapted from a commercial microarray) that quantifies the antibody-mediated inhibition between the receptor angiotensin-converting enzyme 2 (ACE2) and variant-specific receptor-binding domains (RBDs) can assess the neutralizing activity against the SARS-CoV-2 wild-type, and Delta Omicron BA.1, BA.2, and BA.5 subvariants after a booster with Omicron-adapted bivalent vaccines in a manner similar to live-virus NTs. Indeed, by using the live-virus NTs as a reference, we found a significant correlation between the variant-specific NT titers and levels of ACE2-RBD binding inhibition (p < 0.0001, r ≤ 0.78 respectively). Furthermore, the sVNTs identified higher inhibition values against BA.5 and BA.1 in individuals vaccinated with Omicron-adapted vaccines than in those with monovalent wild-type vaccines. Our data thus demonstrate the ability of sVNTs to detect variant-specific nAbs following a booster with bivalent vaccines.
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Springer et al. (2024) conducted an observational in SARS-CoV-2 vaccination and infection (n=95). Multivariant surrogate-virus neutralization test (sVNT) vs. Live-virus neutralization tests (NTs) was evaluated on Correlation between variant-specific NT titers and levels of ACE2-RBD binding inhibition (r ≥ 0.78, p=<0.0001). A novel multivariant surrogate-virus neutralization test showed significant correlation with live-virus neutralization tests (r ≥ 0.78, p < 0.0001) for assessing variant-specific neutralizing antibodies.
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