Evidence map›Paper›PMID 36696921›Full record

ArticleJournal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy2023

Long-term transition of antibody titers in healthcare workers following the first to fourth doses of mRNA COVID-19 vaccine: Comparison of two automated SARS-CoV-2 immunoassays.

Yumi Taniguchi, Koichiro Suemori, Keiko Tanaka, Ai Okamoto, Akiko Murakami, Hitoshi Miyamoto, Yasunori Takasuka, Masakatsu Yamashita, Katsuto Takenaka

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Yumi TaniguchiClinical Laboratory Department, Ehime University Hospital, Ehime, 7910295, Japan.
Koichiro SuemoriDepartment of Hematology, Clinical Immunology and Infectious Diseases, Ehime University Graduate School of Medicine, Ehime, 7910295, Japan. Electronic address: suemori@m.ehime-u.ac.jp.
Keiko TanakaDepartment of Epidemiology and Preventive Medicine, Ehime University Graduate School of Medicine, Ehime, 7910295, Japan.
Ai OkamotoClinical Laboratory Department, Ehime University Hospital, Ehime, 7910295, Japan.
Akiko MurakamiClinical Laboratory Department, Ehime University Hospital, Ehime, 7910295, Japan.
Hitoshi MiyamotoClinical Laboratory Department, Ehime University Hospital, Ehime, 7910295, Japan.
Yasunori TakasukaClinical Laboratory Department, Ehime University Hospital, Ehime, 7910295, Japan.
Masakatsu YamashitaDepartment of Immunology, Ehime University Graduate School of Medicine, Ehime, 7910295, Japan.
Katsuto TakenakaDepartment of Hematology, Clinical Immunology and Infectious Diseases, Ehime University Graduate School of Medicine, Ehime, 7910295, Japan.
Ehime University Hospital · JPEhime University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-spike receptor binding domain (S-RBD) antibody against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which best correlates with virus-neutralizing antibody is useful for estimating the period of protection and identifying the timing of additional booster doses. Long-term transition of the S-RBD antibody titer and the antibody responses among healthy individuals remain unclear. In the present study, therefore, we monitored the S-RBD antibody titers of 16 healthcare workers every 4 weeks for 76 weeks after vaccination with a fourth dose of mRNA-1273 (Moderna) following three doses of BNT162b2 (Pfizer/BioNTech) using two commercial automated immunoassays (Roche and Abbott). Two antibody responses to the vaccine were similar with an up-down change before and after the second (weeks 3), third (weeks 40) and fourth (week 72) vaccinations, but the titer did not fall below the assay's positivity threshold in any individual. The peak level of the geometric mean titer (GMT) in the Roche assay was highest after the third vaccination, and that in Abbott assay was highest after the fourth vaccination but almost equal to that after the third vaccination. Both the geometric mean fold rise (GMFR) demonstrated by the Roche and Abbott assays were highest after the third vaccination. Antibody titers determined by the Roche and Abbott assays showed a positive strong correlation (correlation coefficient: 0.70 to 0.99), but the ratio (Roche/Abbott) of antibodies demonstrated by both assays increased 0.46- to 8.26-fold between weeks 3 and 76. These findings will be helpful for clinicians when interpreting results for SARS-CoV-2 antibody levels and considering future vaccination strategies.

Indexed as

COVID-19SARS-CoV-2Antibodies, ViralBNT162 VaccineCOVID-19 VaccinesHealth PersonnelHumansImmunoassayRNA, MessengerVaccinationAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesRNA, MessengerBNT162bmRNA-1273SARS-CoV-2S-RBD antibodyVaccine

Identifiers

PMID36696921
PMCPMC9867842
OpenAlexW4317702533

What OpenQuestion holds

Textmetadata
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.