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. 2022 Sep;70(9):2552-2560.
doi: 10.1111/jgs.17837. Epub 2022 May 10.

Anti-spike IgG antibody kinetics following the second and third doses of BNT162b2 vaccine in nursing home residents

Affiliations

Anti-spike IgG antibody kinetics following the second and third doses of BNT162b2 vaccine in nursing home residents

Helene Jeulin et al. J Am Geriatr Soc. 2022 Sep.

Abstract

Background: Duration of post-vaccination protection against COVID-19 in nursing home (NH) residents is a critical issue. The objective of this study was to estimate the duration of the IgG(S) response to the mRNA BNT162b2 vaccine in NH residents with (COV-Yes) or without (COV-No) history of SARS-CoV-2 infection.

Methods: A 574 COV-Yes and COV-No NH residents were included in 2 cohorts: Main (n = 115, median age 87 years) or Confirmatory (n = 459, median age 89 years). IgG(S) quantification was carried out at three different time points following the BNT162b2 vaccine: three (1st) and seven (2nd) months after the 2nd dose, and 1 month after the 3rd dose (3rd quantification) in the Main cohort, and twice (2nd and 3rd) in the Confirmatory cohort. The seroneutralization capacity according to COVID-19 history was also measured in a subgroup of patients.

Results: Neutralization capacity was strongly correlated with IgG(S) levels (R2 :76%) without any difference between COV-Yes and COV-No groups for the same levels of IgG(S). After the 2nd dose, duration of the assumed robust protection (IgG(S) >264 BAU/ml) was two-fold higher in the COV-Yes vs. COV-No group: 12.60 (10.69-14.44) versus 5.76 (3.91-8.64) months, with this advantage mainly due to the higher IgG(S) titers after the 2nd dose and secondary to a slower decay over time. After the 3rd dose, duration of robust protection was estimated at 11.87 (9.88-14.87) (COV-Yes) and 8.95 (6.85-11.04) (COV-No) months. These results were similar in both cohorts.

Conclusions and relevance: In old subjects living in NH, history of SARS-CoV-2 infection provides a clear advantage in the magnitude and duration of high IgG(S) titers following the 2nd dose. Importantly, the 3rd dose induces a much more pronounced IgG(S) response than the 2nd dose in COV-No subjects, the effect of which should be able to ensure a prolonged protection against severe forms of COVID-19 in these subjects.

Keywords: SARS-CoV-2; nursing homes; vaccination.

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Conflict of interest statement

The authors have declared no competing interest.

Figures

FIGURE 1
FIGURE 1
Study flowchart. *Among COV‐Yes subjects, 20 out of 74 in the Main cohort and 7 out of 93 in the Confirmatory cohort had SARS‐CoV‐2 infection a few days after the 2nd vaccine dose (February–March 2021). All other subjects had SARS‐CoV‐2 infection prior to the 1st vaccine dose.
FIGURE 2
FIGURE 2
Classification of the subjects in four IgG(S) level categories (BAU/ml) during the 1st (left), 2nd (middle) and 3rd (right) quantification according to history of SARS‐CoV‐2 contamination in the Main (upper) and the Confirmatory (lower) cohorts
FIGURE 3
FIGURE 3
Distribution of IgG(S) levels according to time after the second dose of vaccine and COVID‐19 status in the Main (left) and Confirmatory (right) cohorts. IgG is represented in logarithmic scale. Solid lines represent the predictions from the model and dotted lines the 95% confidence interval. The horizontal black dotted lines correspond to the IgG(S) titers of negative serology 34 BAU/ml) and of “robust” protection (264 BAU/ml) In the Main cohort, each individual is represented twice corresponding to the 1st and the 2nd IgG(S) quantifications in accordance with the linear mixed model described in the Methods section.

References

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