TY - JOUR
T1 - Real-world effectiveness and antibody responses of BNT162b2 vaccination in long-term care residents
T2 - A retrospective case-control study
AU - Unseld, Matthias
AU - Sturtzel, Bärbel
AU - Meyer, Alexa Leonie
AU - Blaise, Marie
AU - Harutyunyan, Lusine
AU - Eger, Nicole
AU - Kautzky-Willer, Alexandra
AU - Dorner, Thomas Ernst
AU - Ohrenberger, Gerald
AU - Mikula, Pavol
AU - Heppner, Hans Jürgen
AU - Zeilinger, Elisabeth Lucia
N1 - Publisher Copyright:
© 2026 The Author(s).
PY - 2026/7
Y1 - 2026/7
N2 - Objectives Older adults in long-term care (LTC) facilities are at high risk for COVID-19–related morbidity and mortality, yet real-world evidence on vaccine effectiveness and immunogenicity in very old populations remains limited. This study evaluated the effectiveness of BNT162b2 vaccination against SARS-CoV-2 infection and assessed post-vaccination antibody responses among institutionalised older adults, including residents aged ≥95 years. Methods A retrospective case–control study was conducted in a geriatric LTC facility in Vienna, Austria. Thirty-eight residents with confirmed SARS-CoV-2 infection were matched to 76 non-infected controls by age, sex, and nutritional risk. Vaccine effectiveness (VE) was estimated using odds ratios (ORs) for infection. Antibody concentrations were analysed in vaccinated residents without prior infection, with adequate response defined as ≥120.1 AU/ml. Results Vaccination was associated with a significantly reduced risk of infection (OR 0.20; 95% CI: 0.07-0.55), corresponding to a VE of 80%. Among residents aged ≥95 years, VE was 94% (95% CI: 28-99%). Overall, 82.8% of vaccinated residents achieved adequate antibody concentrations, with no significant association between age and antibody levels. Among those aged ≥95 years, 90.9% reached adequate antibody concentrations. Conclusions BNT162b2 vaccination provided substantial protection and robust antibody responses among LTC residents, including those of very advanced age, supporting the effectiveness of mRNA vaccination in highly vulnerable institutionalised populations.
AB - Objectives Older adults in long-term care (LTC) facilities are at high risk for COVID-19–related morbidity and mortality, yet real-world evidence on vaccine effectiveness and immunogenicity in very old populations remains limited. This study evaluated the effectiveness of BNT162b2 vaccination against SARS-CoV-2 infection and assessed post-vaccination antibody responses among institutionalised older adults, including residents aged ≥95 years. Methods A retrospective case–control study was conducted in a geriatric LTC facility in Vienna, Austria. Thirty-eight residents with confirmed SARS-CoV-2 infection were matched to 76 non-infected controls by age, sex, and nutritional risk. Vaccine effectiveness (VE) was estimated using odds ratios (ORs) for infection. Antibody concentrations were analysed in vaccinated residents without prior infection, with adequate response defined as ≥120.1 AU/ml. Results Vaccination was associated with a significantly reduced risk of infection (OR 0.20; 95% CI: 0.07-0.55), corresponding to a VE of 80%. Among residents aged ≥95 years, VE was 94% (95% CI: 28-99%). Overall, 82.8% of vaccinated residents achieved adequate antibody concentrations, with no significant association between age and antibody levels. Among those aged ≥95 years, 90.9% reached adequate antibody concentrations. Conclusions BNT162b2 vaccination provided substantial protection and robust antibody responses among LTC residents, including those of very advanced age, supporting the effectiveness of mRNA vaccination in highly vulnerable institutionalised populations.
KW - Antibody response
KW - BNT162b2
KW - COVID-19
KW - Long-term care facilities
KW - Older adults
KW - Vaccine effectiveness
UR - https://www.scopus.com/pages/publications/105037321182
U2 - 10.1016/j.ijid.2026.108682
DO - 10.1016/j.ijid.2026.108682
M3 - Article
C2 - 41935610
AN - SCOPUS:105037321182
SN - 1201-9712
VL - 168
JO - International Journal of Infectious Diseases
JF - International Journal of Infectious Diseases
M1 - 108682
ER -