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. 2021 Mar 27;397(10280):1178-1181.
doi: 10.1016/S0140-6736(21)00502-X. Epub 2021 Feb 25.

Effect of previous SARS-CoV-2 infection on humoral and T-cell responses to single-dose BNT162b2 vaccine

Affiliations

Effect of previous SARS-CoV-2 infection on humoral and T-cell responses to single-dose BNT162b2 vaccine

Maria Prendecki et al. Lancet. .
No abstract available

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Figures

Figure
Figure
Immunological responses to a single dose of BNT162b2 mRNA vaccine (A) Anti-S antibody titres 21–25 days after vaccination in individuals who were infection-naïve or had evidence of previous natural infection. Datapoints with open circles represent five individuals who, despite a negative serological test at baseline, were identified as having previous infection due to reactivity to non-spike peptides on ELISpot testing post-vaccination (which could not have been induced by vaccine alone). Dotted line indicates median anti-spike titre in a cohort of health-care workers 2–8 weeks after PCR-confirmed natural infection with SARS-CoV-2 (n=23, IQR 463–3621). (B) Correlation of post-vaccination anti-spike titre with age in infection-naïve participants. (C) SARS-CoV-2 live virus neutralising antibody titres in the eight individuals with paired results available (n=4 infection-naïve, n=4 with previous natural infection. (D) SARS-CoV-2 live virus neutralising antibody titres post-vaccination in infection-naïve individuals and individuals with previous infection. (E) T-cell responses to SARS-CoV-2 peptide pools post-vaccination in infection-naïve individuals and individuals with previous infection. Peptide pool 1 and peptide pool 2 contain spike protein peptides S1 and S2. Dotted lines indicate mean plus 3 standard deviation for each peptide pool calculated from infection naïve, unvaccinated individuals (48, 43, 26, 33, and 26 SFU/106 PBMC for peptide pools 1–5 respectively). (F) T-cell responses to spike protein peptides of SARS-CoV-2 post-vaccination in infection-naïve and previously infected participants. Inset shows example of ELISpot for an infection-naïve and a previously infected individual for the 2 spike peptide wells. Dotted line indicates mean plus 3 standard deviation for spike peptide pool reactivity calculated from infection naïve, unvaccinated individuals. All data are median with IQR. Statistical analysis was by Kruskall-Wallis test with Dunns' post-hoc correction (A), Spearman rank correlation (B) and Mann-Whitney test (D, F). SFU=spot forming unit. PBMC=peripheral blood mononuclear cells. NT50= neutralisation titres that achieved 50% neutralisation.

References

    1. Polack FP, Thomas SJ, Kitchin N, et al. Safety and efficacy of the BNT162b2 mRNA Covid-19 vaccine. New Eng J Med. 2020;383:2603–2615. - PMC - PubMed
    1. Walsh EE, Frenck RW, Jr, Falsey AR, et al. Safety and immunogenicity of two RNA-based Covid-19 vaccine candidates. New Eng J Med. 2020;383:2439–2450. - PMC - PubMed
    1. Ewer KJ, Barrett JR, Belij-Rammerstorfer S, et al. T cell and antibody responses induced by a single dose of ChAdOx1 nCoV-19 (AZD1222) vaccine in a phase 1/2 clinical trial. Nature Med. 2020;27:270–278. - PubMed
    1. Baden LR, El Sahly HM, Essink B, et al. Efficacy and safety of the mRNA-1273 SARS-CoV-2 vaccine. New Eng J Med. 2021;384:403–416. - PMC - PubMed
    1. Voysey M, Clemens SAC, Madhi SA, et al. Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) against SARS-CoV-2: an interim analysis of four randomised controlled trials in Brazil, South Africa, and the UK. Lancet. 2021;397:99–111. - PMC - PubMed

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