To the Editor:
The emergence of two variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) — B.1.1.7 in the United Kingdom and B.1.351 in South Africa — has aroused concern that these variants may escape immunity resulting from either previous infection or vaccination. In an attempt to measure the resistance of these variants to neutralization elicited by infection or vaccination, we generated recombinant vesicular stomatitis virus–based SARS-CoV-2 pseudoviruses containing the spike protein of the Wuhan-1 reference strain (wild-type), the D614G mutation, and the B.1.1.7 and B.1.351 variants. (Details regarding the recombination process are provided in the Supplementary Appendix, available with the full text of this letter at NEJM.org.)
Neutralization of SARS-CoV-2 Pseudoviruses in Convalescent and Vaccinee Serum Samples.
Panel A shows the 50% pseudovirus neutralization titer (pVNT50) in convalescent serum collected from 34 recovered patients approximately 5 months after SARS-CoV-2 infection and in serum collected from 50 vaccinees who had received either the BBIBP-CorV or CoronaVac vaccine 2 to 3 weeks after the second dose against recombinant vesicular stomatitis virus–based SARS-CoV-2 pseudovirus bearing the Wuhan-1 (wild-type) spike protein. Box plots indicate the median and interquartile range (IQR); the whiskers represent 1.5 times the IQR. Panel B shows changes in the reciprocal serum pVNT50 titer in 34 convalescent serum samples against the D614G, B.1.1.7, and B.1.351 variants, as compared with wild-type virus. Panels C and D show changes in the reciprocal pVNT50 titer in serum samples obtained from the 25 recipients of the BBIBP-CorV vaccine and 25 recipients of the CoronaVac vaccine, respectively, against the D614G, B.1.1.7, and B.1.351 variants, as compared with wild-type virus. Factor changes in the geometric mean titer and 95% confidence interval (CI) in the pVNT50 titers, as compared with those for wild-type virus, are shown under the P values. Only P values of less than 0.05 (indicating significance) are shown. Each data point is the average of duplicate assay results. In each panel, the horizontal dashed line represents the lower limit of detection of the assay (titer, <30); this limit was assigned a value of 10 for geometric mean calculations and was considered to be seronegative. In all panels, calculations were performed with the use of the two-tailed Kruskal–Wallis test after adjustment for the false discovery rate.
We next evaluated pseudovirus resistance to neutralization using convalescent serum obtained from 34 patients 5 months after infection with coronavirus disease 2019 (Covid-19) and serum from 50 participants obtained 2 to 3 weeks after receipt of the second dose of inactivated-virus vaccines — BBIBP-CorV (Sinopharm)1 or CoronaVac (Sinovac)2 — which were developed in China (Table S1 in the Supplementary Appendix). We first determined the serum neutralizing-antibody titer against wild-type pseudovirus and observed similar geometric mean titers (GMTs) in serum obtained from convalescent patients and from vaccinees (Figure 1A), which suggested a low antibody response after two-dose inoculation induced by BBIBP-CorV or CoronaVac.1,2 Notably, undetectable neutralization titers were seen in 4 of 34 convalescent serum samples, in 6 of 25 BBIBP-CorV serum samples, and in 4 of 25 CoronaVac serum samples.
We next assessed the neutralizing activity of convalescent serum and vaccinee serum against D614G, B.1.1.7, and B.1.351 variants as compared with wild-type pseudovirus. The convalescent serum was significantly more effective (by a factor of 2.4; 95% confidence interval [CI], 1.9 to 3.0) in neutralizing the D614G pseudovirus, had a similar effect to that of the wild-type virus in neutralizing the B.1.1.7 variant, and was significantly less effective (by a factor of 0.5; 95% CI, 0.4 to 0.7) in neutralizing the B.1.351 pseudovirus (Figure 1B). Moreover, 9 of 30 convalescent serum samples showed complete loss of neutralizing activity against B.1.351. For the BBIBP-CorV vaccinee serum samples, although the GMTs of neutralization against the variants were not significantly different from the GMTs…
Read More: Susceptibility of Circulating SARS-CoV-2 Variants to Neutralization
