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. 2024 Aug 22;12(8):951.
doi: 10.3390/vaccines12080951.

Follow-Up of SARS-CoV-2 Antibody Levels in Belgian Nursing Home Residents and Staff Two, Four and Six Months after Primary Course BNT162b2 Vaccination

Affiliations

Follow-Up of SARS-CoV-2 Antibody Levels in Belgian Nursing Home Residents and Staff Two, Four and Six Months after Primary Course BNT162b2 Vaccination

Eline Meyers et al. Vaccines (Basel). .

Abstract

When COVID-19 vaccines were implemented, nursing home residents (NHRs) and staff (NHS) in Belgium were prioritized for vaccination. To characterize the vaccine response over time in this population and to identify poorly responding groups, we assessed antibody concentrations two (T1), four (T2) and six months (T3) after primary course BNT162b2 vaccination in six groups of infection-naive/infection-primed NHRs/NHS, with/without comorbidity (NHRs only). Participant groups (N = 125 per group) were defined within a national serosurveillance study in nursing homes, based on questionnaire data. Dried blood spots were analyzed using ELISA for the quantification of SARS-CoV-2 S1RBD IgG antibodies. Among all groups, antibody concentrations significantly decreased between T1 and T2/T3, all with a ≥70% decrease at T3, except for infection-primed staff (-32%). Antibody concentrations among infection-naive NHRs were 11.96 times lower than those among infection-primed NHR, while the latter were comparable (x1.05) to infection-primed NHS. The largest proportion [13% (95% CI: 11-24%)] of vaccine non-responders was observed in the group of infection-naive NHRs with comorbidities. A longer interval between infection and vaccination (≥3 months) elicited higher antibody responses. Our data retrospectively show the necessity of timely COVID-19 booster vaccination. Infection-naive NHRs require special attention regarding immune monitoring in future epidemics or pandemics.

Keywords: COVID-19 vaccination; SARS-CoV-2 antibodies; nursing home residents; nursing home staff.

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Conflict of interest statement

The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Overview of the timing of the primary course vaccination campaign in Belgian nursing homes and sampling timepoints in the study (approximately two months (T1), four months (T2) and six months (T3) after vaccination). Vertical white dashed lines indicate three-month timespans.
Figure 2
Figure 2
S1RBD IgG antibody concentrations in nursing home residents and staff two (T1), four (T2) and six months (T3) after two-dose regimen BNT162b2 vaccination. S1RBD IgG antibody concentrations over time are visualized per sub-cohort by spaghetti plots (left) and box plots (right). Panel (A): Infection-naive residents, no comorbidity. Panel (B): Infection-primed residents, no comorbidity. Panel (C): Infection-naive staff, no comorbidity. Panel (D): Infection-primed staff, no comorbidity. Panel (E): Infection-naive residents, ≥1 comorbidity. Panel (F): Infection-primed residents, ≥1 comorbidity. **** = adjusted p ≤ 0.0001, *** = adjusted p ≤ 0.001, ** = adjusted p ≤ 0.01, ns = adjusted p > 0.05. Percentages with 95% confidence intervals below the boxplot indicate the decrease in geometric mean antibody concentration between T1 and T2 post-vaccination (below middle boxplot), between T2 and T3 (upper value below right boxplot) and between T1 and T3 (lower value below right boxplot). Lower and upper error bars represent the minimum and maximum S1RBD IgG concentrations, respectively.

References

    1. Catteau L., Haarhuis F., Dequeker S., Vandael E., Stouten V., Litzroth A., Wyndham Thomas C. Surveillance de la Vaccination COVID-19 Dans les Maisons de Repos et Maisons de Repos et de Soins Belges. Sciensano; Bruxelles, Belgique: 2021.
    1. Polack F.P., Thomas S.J., Kitchin N., Absalon J., Gurtman A., Lockhart S., Perez J.L., Pérez Marc G., Moreira E.D., Zerbini C., et al. Safety and Efficacy of the BNT162b2 mRNsA COVID-19 Vaccine. N. Engl. J. Med. 2020;383:2603–2615. doi: 10.1056/NEJMoa2034577. - DOI - PMC - PubMed
    1. Walsh E.E., Frenck R.W., Jr., Falsey A.R., Kitchin N., Absalon J., Gurtman A., Lockhart S., Neuzil K., Mulligan M.J., Bailey R., et al. Safety and Immunogenicity of Two RNA-Based COVID-19 Vaccine Candidates. N. Engl. J. Med. 2020;383:2439–2450. doi: 10.1056/NEJMoa2027906. - DOI - PMC - PubMed
    1. High K.P., Fulop T., Pawelec G., Castle S., Loeb M. Immunosenescence and Vaccination in Nursing Home Residents. Clin. Infect. Dis. 2009;48:443–448. doi: 10.1086/596475. - DOI - PubMed
    1. Thomas S.J., Moreira E.D., Kitchin N., Absalon J., Gurtman A., Lockhart S., Perez J.L., Pérez Marc G., Polack F.P., Zerbini C., et al. Safety and Efficacy of the BNT162b2 mRNA COVID-19 Vaccine through 6 Months. N. Engl. J. Med. 2021;385:1761–1773. doi: 10.1056/NEJMoa2110345. - DOI - PMC - PubMed

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