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Three-month follow-up of durability of response to the third dose of the SARS-CoV-2 BNT162b2 vaccine in adults aged 60 years and older: a prospective cohort study

OBJECTIVE: To evaluate the durability of response 3 months after the third BNT162b2 vaccine in adults aged 60 years and older. DESIGN: Prospective cohort study. SETTING: Single tertiary centre. PARTICIPANTS: Healthcare workers/family members aged ≥60 years old who received the third BNT162b2 dose. I...

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Autores principales: Eliakim-Raz, Noa, Stemmer, Amos, Leibovici-Weisman, Yaara, Ness, Asaf, Awwad, Muhammad, Ghantous, Nassem, Erez, Noam, Bareket-Samish, Avital, Levy-Barda, Adva, Ben-Zvi, Haim, Moskovits, Neta, Bar-Haim, Erez, Stemmer, Salomon M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350740/
https://www.ncbi.nlm.nih.gov/pubmed/35918111
http://dx.doi.org/10.1136/bmjopen-2022-061584
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author Eliakim-Raz, Noa
Stemmer, Amos
Leibovici-Weisman, Yaara
Ness, Asaf
Awwad, Muhammad
Ghantous, Nassem
Erez, Noam
Bareket-Samish, Avital
Levy-Barda, Adva
Ben-Zvi, Haim
Moskovits, Neta
Bar-Haim, Erez
Stemmer, Salomon M
author_facet Eliakim-Raz, Noa
Stemmer, Amos
Leibovici-Weisman, Yaara
Ness, Asaf
Awwad, Muhammad
Ghantous, Nassem
Erez, Noam
Bareket-Samish, Avital
Levy-Barda, Adva
Ben-Zvi, Haim
Moskovits, Neta
Bar-Haim, Erez
Stemmer, Salomon M
author_sort Eliakim-Raz, Noa
collection PubMed
description OBJECTIVE: To evaluate the durability of response 3 months after the third BNT162b2 vaccine in adults aged 60 years and older. DESIGN: Prospective cohort study. SETTING: Single tertiary centre. PARTICIPANTS: Healthcare workers/family members aged ≥60 years old who received the third BNT162b2 dose. INTERVENTIONS: Blood samples were drawn immediately before (T0), 10–19 days (T1) and 74–103 days (T2) after the third dose. PRIMARY AND SECONDARY OUTCOME MEASURES: Anti-spike IgG titres were determined using a commercial assay and seropositivity was defined as ≥50 arbitrary units (AU)/mL. Neutralising antibody titres were determined at T2. Adverse events, COVID-19 infections and Clinical Frailty Scale (CFS) levels were documented. RESULTS: The analysis included 97 participants (median age, 70 years (IQR, 66–74), 58% CFS level 2). IgG titres, which increased significantly from T0 to T1 (median, 440 AU/mL (IQR, 294–923) and median, 25 429 AU/mL (IQR, 14 203–36 114), respectively; p<0.001), decreased significantly by T2, but all remained seropositive (median, 8306 AU/mL (IQR, 4595–14 701), p<0.001 vs T1). In a multivariable analysis, only time from the second vaccine was significantly associated with lower IgG levels at T2 (p=0.017). At T2, 60 patients were evaluated for neutralising antibodies; all were seropositive (median, 1294 antibody titres; IQR, 848–2072). Neutralising antibody and anti-spike IgG levels were correlated (r=0.6, p<0.001). No major adverse events or COVID-19 infections were reported. CONCLUSIONS: Anti-spike IgG and neutralising antibody levels remain adequate 3 months after the third BNT162b2 vaccine in healthy adults aged ≥60 years, although the decline in IgG is concerning. A third dose of vaccine in this population should be top priority.
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spelling pubmed-93507402022-08-09 Three-month follow-up of durability of response to the third dose of the SARS-CoV-2 BNT162b2 vaccine in adults aged 60 years and older: a prospective cohort study Eliakim-Raz, Noa Stemmer, Amos Leibovici-Weisman, Yaara Ness, Asaf Awwad, Muhammad Ghantous, Nassem Erez, Noam Bareket-Samish, Avital Levy-Barda, Adva Ben-Zvi, Haim Moskovits, Neta Bar-Haim, Erez Stemmer, Salomon M BMJ Open Infectious Diseases OBJECTIVE: To evaluate the durability of response 3 months after the third BNT162b2 vaccine in adults aged 60 years and older. DESIGN: Prospective cohort study. SETTING: Single tertiary centre. PARTICIPANTS: Healthcare workers/family members aged ≥60 years old who received the third BNT162b2 dose. INTERVENTIONS: Blood samples were drawn immediately before (T0), 10–19 days (T1) and 74–103 days (T2) after the third dose. PRIMARY AND SECONDARY OUTCOME MEASURES: Anti-spike IgG titres were determined using a commercial assay and seropositivity was defined as ≥50 arbitrary units (AU)/mL. Neutralising antibody titres were determined at T2. Adverse events, COVID-19 infections and Clinical Frailty Scale (CFS) levels were documented. RESULTS: The analysis included 97 participants (median age, 70 years (IQR, 66–74), 58% CFS level 2). IgG titres, which increased significantly from T0 to T1 (median, 440 AU/mL (IQR, 294–923) and median, 25 429 AU/mL (IQR, 14 203–36 114), respectively; p<0.001), decreased significantly by T2, but all remained seropositive (median, 8306 AU/mL (IQR, 4595–14 701), p<0.001 vs T1). In a multivariable analysis, only time from the second vaccine was significantly associated with lower IgG levels at T2 (p=0.017). At T2, 60 patients were evaluated for neutralising antibodies; all were seropositive (median, 1294 antibody titres; IQR, 848–2072). Neutralising antibody and anti-spike IgG levels were correlated (r=0.6, p<0.001). No major adverse events or COVID-19 infections were reported. CONCLUSIONS: Anti-spike IgG and neutralising antibody levels remain adequate 3 months after the third BNT162b2 vaccine in healthy adults aged ≥60 years, although the decline in IgG is concerning. A third dose of vaccine in this population should be top priority. BMJ Publishing Group 2022-08-02 /pmc/articles/PMC9350740/ /pubmed/35918111 http://dx.doi.org/10.1136/bmjopen-2022-061584 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Infectious Diseases
Eliakim-Raz, Noa
Stemmer, Amos
Leibovici-Weisman, Yaara
Ness, Asaf
Awwad, Muhammad
Ghantous, Nassem
Erez, Noam
Bareket-Samish, Avital
Levy-Barda, Adva
Ben-Zvi, Haim
Moskovits, Neta
Bar-Haim, Erez
Stemmer, Salomon M
Three-month follow-up of durability of response to the third dose of the SARS-CoV-2 BNT162b2 vaccine in adults aged 60 years and older: a prospective cohort study
title Three-month follow-up of durability of response to the third dose of the SARS-CoV-2 BNT162b2 vaccine in adults aged 60 years and older: a prospective cohort study
title_full Three-month follow-up of durability of response to the third dose of the SARS-CoV-2 BNT162b2 vaccine in adults aged 60 years and older: a prospective cohort study
title_fullStr Three-month follow-up of durability of response to the third dose of the SARS-CoV-2 BNT162b2 vaccine in adults aged 60 years and older: a prospective cohort study
title_full_unstemmed Three-month follow-up of durability of response to the third dose of the SARS-CoV-2 BNT162b2 vaccine in adults aged 60 years and older: a prospective cohort study
title_short Three-month follow-up of durability of response to the third dose of the SARS-CoV-2 BNT162b2 vaccine in adults aged 60 years and older: a prospective cohort study
title_sort three-month follow-up of durability of response to the third dose of the sars-cov-2 bnt162b2 vaccine in adults aged 60 years and older: a prospective cohort study
topic Infectious Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350740/
https://www.ncbi.nlm.nih.gov/pubmed/35918111
http://dx.doi.org/10.1136/bmjopen-2022-061584
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