Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Dec;10(1):1241-1243.
doi: 10.1080/22221751.2021.1940305.

Serosurvey in BNT162b2 vaccine-elicited neutralizing antibodies against authentic B.1, B.1.1.7, B.1.351, B.1.525 and P.1 SARS-CoV-2 variants

Affiliations

Serosurvey in BNT162b2 vaccine-elicited neutralizing antibodies against authentic B.1, B.1.1.7, B.1.351, B.1.525 and P.1 SARS-CoV-2 variants

Alberto Zani et al. Emerg Microbes Infect. 2021 Dec.

Abstract

In this study, we show that BNT162b2 vaccine-elicited antibodies efficiently neutralize SARS-CoV-2 authentic viruses belonging to B.1, B.1.1.7, B.1.351, B.1.525 and P.1 lineages. Interestingly, the neutralization of B.1.1.7 and B.1.525 lineages was significantly higher, whereas the neutralization of B.1.351 and P.1 lineages was robust but significantly lower as compared to B.1 lineage. Following our findings, we consider that the BNT162b2 vaccine offers protection against the current prevailing variants of SARS-CoV-2.

Keywords: BNT162b2 vaccine; SARS-CoV-2; neutralizing antibodies; variant of concern; variant of interest.

PubMed Disclaimer

Conflict of interest statement

No potential conflict of interest was reported by the author(s).

Figures

Figure 1.
Figure 1.
Serum neutralization of authentic SARS-CoV-2 B.1 lineage and its viral variants. (A) SARS-CoV-2 B.1 lineage and SARS-CoV-2 B.1.1.7 lineage. (B) SARS-CoV-2 B.1 lineage and SARS-CoV-2 B.1.351 lineage. (C) SARS-CoV-2 B.1 lineage and SARS-CoV-2 B.1.525 lineage. (D) SARS-CoV-2 B.1 lineage and SARS-CoV-2 P.1 lineage. Shown are the results of neutralization test with the use of 37 samples obtained from 37 volunteers between 10 and 20 days after the administration of the second dose of the BNT162b2 vaccine (which occurred three weeks after the first immunization). Neutralization of authentic viruses was performed by cytopathic effect (CPE)-based assay using a viral titre of 102 TCID50. The neutralization titre of the serum sample was calculated as the reciprocal of the highest dilution that protected more than 50% of cells from CPE. Sera with different neutralization titre against SARS-CoV-2 B.1 lineage and viral variants are connected by lines. Horizontal lines and the numbers over the bars indicate geometric mean titres (GM). The I bars indicate 95% confidence intervals. Statistical analysis was performed using the paired t-test and two-tailed P values were calculated. The statistical significance of the difference between neutralization titres in the SARS-CoV-2 B.1 lineage and in each variant virus neutralization assay with the same serum samples are as follows: P < .0001 for SARS-CoV-2 B.1.1.7 lineage; P < .0001 for SARS-CoV-2 B.1.351 lineage; and P < .0001 for SARS-CoV-2 B.1.525 lineage; and P = .0002 for SARS-CoV-2 P.1 lineage.

Similar articles

Cited by

References

    1. Polack FP, Thomas SJ, Kitchin N, et al. . Safety and efficacy of the BNT162b2 mRNA Covid-19 vaccine. N Engl J Med. 2020 Dec 31;383(27):2603–2615. - PMC - PubMed
    1. Liu Y, Liu J, Xia H, et al. . Neutralizing activity of BNT162b2-elicited serum. N Engl J Med. 2021; 384(15):1466–1468. - PMC - PubMed
    1. Andreano E, Nicastri E, Paciello I, et al. . Extremely potent human monoclonal antibodies from COVID-19 convalescent patients. Cell. 2021;184(7):1821–1835.e16. - PMC - PubMed
    1. Starr TN, Greaney AJ, Hilton SK, et al. . Deep mutational scanning of SARS-CoV-2 receptor binding domain reveals constraints on folding and ACE2 binding. Cell. 2020;182:1295–1310.e20. - PMC - PubMed
    1. Nelson G, Buzko O, Spilman P, et al. Molecular dynamic simulation reveals E484K mutation enhances spike RBD-ACE2 affinity and the combination of E484K, K417N and N501Y mutations (501Y.V2 variant) induces conformational change greater than N501Y mutant alone, potentially resulting in an escape mutant. bioRxiv. 2021 (10.1101/2021.01.13.426558). Preprint. - DOI