P-2058. Neutralizing Antibody Kinetics and Projected Immunity up to 12-months after COVID Vaccination in Nursing Home Residents

Abstract Background Immune response and memory changes with aging and disease, features that may be amplified in long-term care populations. We evaluated the kinetics of immunity following vaccination and infection in nursing home residents (NHR). Methods In a cohort of NHR with continuous enrollment since 2020, we drew blood before and after mRNA COVID-19 vaccines and SARS-COV-2 infection. We identified prior and breakthrough infections and the intervals between vaccinations and samples to describe decay kinetics of neutralizing titers over time. Assuming a peak response occurring 14 days after each dose, we estimated mixed-effects exponential decay models, stratified by dose and prior infection and assuming a random intercept for each subject. From these models, we estimated peak value and rates of decay for Wuhan and Omicron BA.4/5 neutralizing titers. Results Our analysis cohort followed 412 NHR (median (IQR) age = 76 (69, 86); 49% female). Among infection-naive NHR, the estimated Wuhan rate of decay did not differ significantly across doses. Prior infected NHR showed significantly longer half-lives after all booster doses than with the primary series (Figure 1, Table 1). Decay models of Omicron BA.4/5 neutralizing titers following booster doses showed significant increases in peak titer for each subsequent booster among both the naive and prior infection subgroups. The decay rates increased significantly over the first monovalent booster, but no differences in rates were detected between infection-naive and prior infection subgroups (Figure 2). The estimated half-lives across strain, dose, and infection subgroups ranged from roughly 50 to 150 days; the differences in peak and decay are reflected in the predicted titers at 6 and 12 months after vaccination (Table 2). Conclusion Following primary series and booster doses, NHR with prior infection enjoy both higher peaks and a similar or slower decline in neutralizing titers than naive NHR, demonstrating the benefits of hybrid immunity with subsequent vaccinations. Neutralizing titers decline sufficiently fast to warrant updating vaccines before the prior dose anniversary. Understanding the kinetics of serial doses within this population can assist in vaccine planning and priorities among NHR. Disclosures Yasin Abul, MD, Moderna: Grant/Research Support|Moderna, Abt, CDC: Grant/Research Support Alejandro Balazs, PhD, Cure Systems LLC: Ownership Interest Stefan Gravenstein, MD, MPH, CDC: Advisor/Consultant|CDC: Grant/Research Support|Genentech: Advisor/Consultant|Genentech: Grant/Research Support|Genentech: Honoraria|GlaxoSmithKline: Advisor/Consultant|GlaxoSmithKline: Grant/Research Support|GlaxoSmithKline: Honoraria|Janssen: Advisor/Consultant|Janssen: Grant/Research Support|Janssen: Honoraria|Moderna: Advisor/Consultant|Moderna: Grant/Research Support|Moderna: Honoraria|NIH: Grant/Research Support|Pfizer: Advisor/Consultant|Pfizer: Grant/Research Support|Pfizer: Honoraria|Sanofi: Advisor/Consultant|Sanofi: Grant/Research Support|Sanofi: Honoraria|Seqirus: Advisor/Consultant David Canaday, MD, Moderna: Grant/Research Support|Pfizer: Grant/Research Support

Authors

Institutions

Publication Details

Journal
Open Forum Infectious Diseases
Published
2025-01-29
DOI
https://doi.org/10.1093/ofid/ofae631.2214
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

P-2058. Neutralizing Antibody Kinetics and Projected Immunity up to 12-months after COVID Vaccination in Nursing Home Residents

Nicholas Sundheimer, Yi Cao, Christopher L. King, Clare Nugent et al.
Open Forum Infectious Diseases
SARS-CoV-2 and COVID-19 Research
article

P-2058. Neutralizing Antibody Kinetics and Projected Immunity up to 12-months after COVID Vaccination in Nursing Home Residents

Nicholas Sundheimer, Yi Cao, Christopher L. King, Clare Nugent, Stefan Gravenstein, Alejandro B. Balazs, Brigid Wilson, David H. Canaday, Vaishnavi Ragavapuram, Alexandra Paxitzis, Olajide Olagunju, Michael C. Payne, Oladayo A Oyebanji, Jürgen Bosch, Yasin Abul
article en

Abstract

Abstract Background Immune response and memory changes with aging and disease, features that may be amplified in long-term care populations. We evaluated the kinetics of immunity following vaccination and infection in nursing home residents (NHR). Methods In a cohort of NHR with continuous enrollment since 2020, we drew blood before and after mRNA COVID-19 vaccines and SARS-COV-2 infection. We identified prior and breakthrough infections and the intervals between vaccinations and samples to describe decay kinetics of neutralizing titers over time. Assuming a peak response occurring 14 days after each dose, we estimated mixed-effects exponential decay models, stratified by dose and prior infection and assuming a random intercept for each subject. From these models, we estimated peak value and rates of decay for Wuhan and Omicron BA.4/5 neutralizing titers. Results Our analysis cohort followed 412 NHR (median (IQR) age = 76 (69, 86); 49% female). Among infection-naive NHR, the estimated Wuhan rate of decay did not differ significantly across doses. Prior infected NHR showed significantly longer half-lives after all booster doses than with the primary series (Figure 1, Table 1). Decay models of Omicron BA.4/5 neutralizing titers following booster doses showed significant increases in peak titer for each subsequent booster among both the naive and prior infection subgroups. The decay rates increased significantly over the first monovalent booster, but no differences in rates were detected between infection-naive and prior infection subgroups (Figure 2). The estimated half-lives across strain, dose, and infection subgroups ranged from roughly 50 to 150 days; the differences in peak and decay are reflected in the predicted titers at 6 and 12 months after vaccination (Table 2). Conclusion Following primary series and booster doses, NHR with prior infection enjoy both higher peaks and a similar or slower decline in neutralizing titers than naive NHR, demonstrating the benefits of hybrid immunity with subsequent vaccinations. Neutralizing titers decline sufficiently fast to warrant updating vaccines before the prior dose anniversary. Understanding the kinetics of serial doses within this population can assist in vaccine planning and priorities among NHR. Disclosures Yasin Abul, MD, Moderna: Grant/Research Support|Moderna, Abt, CDC: Grant/Research Support Alejandro Balazs, PhD, Cure Systems LLC: Ownership Interest Stefan Gravenstein, MD, MPH, CDC: Advisor/Consultant|CDC: Grant/Research Support|Genentech: Advisor/Consultant|Genentech: Grant/Research Support|Genentech: Honoraria|GlaxoSmithKline: Advisor/Consultant|GlaxoSmithKline: Grant/Research Support|GlaxoSmithKline: Honoraria|Janssen: Advisor/Consultant|Janssen: Grant/Research Support|Janssen: Honoraria|Moderna: Advisor/Consultant|Moderna: Grant/Research Support|Moderna: Honoraria|NIH: Grant/Research Support|Pfizer: Advisor/Consultant|Pfizer: Grant/Research Support|Pfizer: Honoraria|Sanofi: Advisor/Consultant|Sanofi: Grant/Research Support|Sanofi: Honoraria|Seqirus: Advisor/Consultant David Canaday, MD, Moderna: Grant/Research Support|Pfizer: Grant/Research Support

Open Forum Infectious DiseasesVol. 12(Supplement_1)
Brown University (US), Ragon Institute of MGH, MIT and Harvard (US), VA Northeast Ohio Healthcare System (US), Case Western Reserve University (US)
Openalex Percentile: Top 98%
SARS-CoV-2 and COVID-19 Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.