Evidence map›Paper›PMID 35918111›Full record

ArticleBMJ open2022

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.

Noa Eliakim-Raz, Amos Stemmer, Yaara Leibovici-Weisman, Asaf Ness, Muhammad Awwad, Nassem Ghantous, Noam Erez, Avital Bareket-Samish, Adva Levy-Barda, Haim Ben-Zvi and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Noa Eliakim-Raz *Department of Medicine E and Infectious Diseases Unit, Beilinson Hospital, Petah Tikva, Israel.
Amos Stemmer *Oncology, Sheba Medical Center at Tel Hashomer, Tel Hashomer, Israel.ORCID 0000-0002-2357-3923
Yaara Leibovici-WeismanSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Asaf NessDepartment of Medicine E, Beilinson Hospital, Petah Tikva, Israel.
Muhammad AwwadDepartment of Medicine E, Beilinson Hospital, Petah Tikva, Israel.
Nassem GhantousDepartment of Medicine E, Beilinson Hospital, Petah Tikva, Israel.
Noam ErezDepartment of Infectious Diseases, Israel Institute for Biological Research, Ness Ziona, Israel.
Avital Bareket-SamishBioInsight, Binyamina, Israel.
Adva Levy-BardaBiobank, Department of Pathology, Beilinson Hospital, Petah Tikva, Israel.
Haim Ben-ZviDepartment of Medicine E, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Neta MoskovitsFelsenstein Medical Research Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Erez Bar-HaimDepartment of Biochemistry and Molecular Genetics, Israel Institute for Biological Research, Ness Ziona, Israel.ORCID 0000-0003-3435-8599
Salomon M StemmerSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel salomon.stemmer@gmail.com.
Rabin Medical Center · ILTel Aviv University · ILIsrael Institute for Biological Research · ILSheba Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the durability of response 3 months after the third BNT162b2 vaccine in adults aged 60 years and older.

designProspective cohort study.

settingSingle tertiary centre.

participantsHealthcare workers/family members aged ≥60 years old who received the third BNT162b2 dose.

interventionsBlood 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.

resultsThe 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.

conclusionsAnti-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.

Indexed as

COVID-19AdultAgedAntibodies, NeutralizingAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesFollow-Up StudiesHumansImmunoglobulin GMiddle AgedProspective StudiesSARS-CoV-2Antibodies, NeutralizingAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesImmunoglobulin GCOVID-19EPIDEMIOLOGYIMMUNOLOGY

Identifiers

PMID35918111
PMCPMC9350740
OpenAlexW4289443827

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.