Neutralizing Activity of BNT162b2-Elicited Serum

Abstract

To the Editor: BNT162b2 is a nucleoside-modified RNA vaccine expressing the full-length prefusion spike glycoprotein (S) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). In a randomized, placebo-controlled clinical trial involving approximately 44,000 participants, immunization conferred 95% efficacy against coronavirus disease 2019 (Covid-19). 1 New, highly transmissible SARS-CoV-2 variants that were first detected in the United Kingdom (B.1.1.7 lineage), South Africa (B.1.351 lineage), and Brazil (P.1 lineage) with mutations in the S gene are spreading globally. To analyze effects on neutralization elicited by BNT162b2, we engineered S mutations from each of the three new lineages into USA-WA1/2020, a relatively early isolate of the virus from January 2020 (Fig. S1 in the Supplementary Appendix, available with the full text of this letter at NEJM.org). We thereby produced three recombinant viruses representing each of these lineages and two additional ones in which we engineered subsets of mutations of the B.1.351 lineage. Thus, the first recombinant virus had all the mutations found in the S gene in the B.1.1.7 lineage (B.1.1.7-spike), the second had all the mutations found in the S gene in the P.1 lineage (P.1-spike), the third had all the mutations found in the S gene in the B.1.351 lineage (B.1.351-spike), the fourth had an N-terminal domain deletion found in the B.1.351 lineage and the globally dominant D614G substitution (B.1.351-∆242-244+D614G), and the fifth had the three mutations from the B.1.351 lineage affecting amino acids in the receptor-binding site (K417N, E484K, and N501Y) and a D614G substitution (B.1.351-RBD+D614G). The mutant amino acid residues in the B.1.351-RBD+D614G recombinant virus are also among those in the P.1 lineage virus, although in the P.1 lineage virus, K417 is mutated to threonine rather than asparagine. All the mutant viruses yielded infectious viral titers exceeding 107 plaque-forming units per milliliter. The B.1.1.7-spike and B.1.351-spike viruses formed plaques that were smaller than those formed by the other viruses (Fig. S2). We performed 50% plaque reduction neutralization testing (PRNT50) using 20 serum samples that had been obtained from 15 participants in the pivotal trial 1,2 2 or 4 weeks after the administration of the second dose of 30 μg of BNT162b2 (which occurred 3 weeks after the first immunization) (Fig. S3). All the serum samples efficiently neutralized USA-WA1/2020 and all the viruses with variant spikes. Almost all of them did so at titers higher than 1:40. Geometric mean neutralizing titers against USA-WA1/2020, B.1.1.7-spike, P.1-spike, B.1.351-spike, B.1.351-∆242-244+D614G, and B.1.351-RBD+D614G viruses were 532, 663, 437, 194, 485, and 331, respectively (Figure 1 and Table S1). Thus, as compared with neutralization of USA-WA1/2020, neutralization of B.1.1.7-spike and P.1-spike viruses was roughly equivalent, and neutralization of B.1.351-spike virus was robust but lower. Our data are also consistent with lower neutralization titers against the virus with the full set of B.1.351-spike mutations than against virus with either subset of mutations. Our findings also suggest that mutations that result in amino acid substitutions K417N, E484K, and N501Y in the receptor-binding site have a greater effect on neutralization than the 242–244 deletion affecting the N-terminal domain of the spike protein. Limitations of the study include the potential for mutations to alter neutralization by affecting spike function rather than antigenicity. Therefore, each neutralization assay with a different target virus is unique, and comparisons between neutralization titers from different assays should be interpreted with caution. Neutralizing activity against the B.1.351 lineage virus was robust at a geometric mean titer that was much higher than that obtained after one dose of BNT162b2, when strong efficacy was already observed in the C4591001 efficacy trial. 1-3 T-cell immunity may also be involved in protection, 4 and BNT162b2 immunization elicits CD8+ T-cell responses that recognize multiple variants. 5 Ultimately, conclusions about vaccine-mediated protection that are extrapolated from neutralization or T-cell data must be validated by real-world evidence collected in regions where the SARS-CoV-2 variants are circulating.