Evidence map›Paper›PMID 37311763›Full record

ArticleScientific reports2023

Waning cellular immune responses and predictive factors in maintaining cellular immunity against SARS-CoV-2 six months after BNT162b2 mRNA vaccination.

Takashi Ishii, Kensuke Hamada, Daisuke Jubishi, Hideki Hashimoto, Koh Okamoto, Naoko Hisasue, Mitsuhiro Sunohara, Minako Saito, Takayuki Shinohara, Marie Yamashita and 7 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 13 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

17 authors at 2 institutions in 1 country.

Takashi IshiiDivision for Health Service Promotion, The University of Tokyo, Hongo 7-3-1, Bunkyo, TokyoTokyo, 113-8655, Japan. taishii-tky@umin.ac.jp.
Kensuke HamadaDivision for Health Service Promotion, The University of Tokyo, Hongo 7-3-1, Bunkyo, TokyoTokyo, 113-8655, Japan.
Daisuke JubishiDepartment of Infectious Diseases, The University of Tokyo Hospital, Tokyo, Japan.
Hideki HashimotoDepartment of Infectious Diseases, The University of Tokyo Hospital, Tokyo, Japan.
Koh OkamotoDepartment of Infectious Diseases, The University of Tokyo Hospital, Tokyo, Japan.
Naoko HisasueDivision for Health Service Promotion, The University of Tokyo, Hongo 7-3-1, Bunkyo, TokyoTokyo, 113-8655, Japan.
Mitsuhiro SunoharaDivision for Health Service Promotion, The University of Tokyo, Hongo 7-3-1, Bunkyo, TokyoTokyo, 113-8655, Japan.
Minako SaitoDivision for Health Service Promotion, The University of Tokyo, Hongo 7-3-1, Bunkyo, TokyoTokyo, 113-8655, Japan.
Takayuki ShinoharaDepartment of Infectious Diseases, The University of Tokyo Hospital, Tokyo, Japan.
Marie YamashitaDepartment of Infectious Diseases, The University of Tokyo Hospital, Tokyo, Japan.
Yuji WakimotoDepartment of Infectious Diseases, The University of Tokyo Hospital, Tokyo, Japan.
Amato OtaniDepartment of Infectious Diseases, The University of Tokyo Hospital, Tokyo, Japan.
Mahoko IkedaDepartment of Infectious Diseases, The University of Tokyo Hospital, Tokyo, Japan.
Sohei HaradaDepartment of Infection Control and Prevention, The University of Tokyo Hospital, Tokyo, Japan.
Shu OkugawaDepartment of Infectious Diseases, The University of Tokyo Hospital, Tokyo, Japan.
Kyoji MoriyaDivision for Health Service Promotion, The University of Tokyo, Hongo 7-3-1, Bunkyo, TokyoTokyo, 113-8655, Japan.
Shintaro YanagimotoDivision for Health Service Promotion, The University of Tokyo, Hongo 7-3-1, Bunkyo, TokyoTokyo, 113-8655, Japan. yanagimoto@hc.u-tokyo.ac.jp.
University of Tokyo Hospital · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several clinical trials have shown that the humoral response produced by anti-spike antibodies elicited by coronavirus disease 2019 (COVID-19) vaccines gradually declines. The kinetics, durability and influence of epidemiological and clinical factors on cellular immunity have not been fully elucidated. We analyzed cellular immune responses elicited by BNT162b2 mRNA vaccines in 321 health care workers using whole blood interferon-gamma (IFN-γ) release assays. IFN-γ, induced by CD4 + and CD8 + T cells stimulated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike epitopes (Ag2), levels were highest at 3 weeks after the second vaccination (6 W) and decreased by 37.4% at 3 months (4 M) and 60.0% at 6 months (7 M), the decline of which seemed slower than that of anti-spike antibody levels. Multiple regression analysis revealed that the levels of IFN-γ induced by Ag2 at 7 M were significantly correlated with age, dyslipidemia, focal adverse reactions to full vaccination, lymphocyte and monocyte counts in whole blood, Ag2 levels before the second vaccination, and Ag2 levels at 6 W. We clarified the dynamics and predictive factors for the long-lasting effects of cellular immune responses. The results emphasize the need for a booster vaccine from the perspective of SARS-CoV-2 vaccine-elicited cellular immunity.

Indexed as

BNT162 VaccineCOVID-19COVID-19 VaccinesHumansImmunity, CellularInterferon-gammaRNA, MessengerSARS-CoV-2BNT162 VaccineCOVID-19 VaccinesInterferon-gammaRNA, Messenger

Identifiers

PMID37311763
PMCPMC10263378
OpenAlexW4380577524

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.