Evidence map›Paper›PMID 38216287›Full record

ArticleRMD open2024

Determination of the factors associated with antigen-specific CD4+ T-cell responses to BNT162b2 in patients with rheumatoid arthritis.

Fumiaki Sagawa, Hisakata Yamada, Masahiro Ayano, Yasutaka Kimoto, Hiroki Mitoma, Nobuyuki Ono, Yojiro Arinobu, Masakazu Kondo, Yasuharu Nakashima, Koichi Akashi and 2 more

Open access · goldAbstract read
In one paragraph

Article in RMD open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 99% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 4 institutions in 1 country.

Fumiaki SagawaDepartment of Medicine and Biosystemic Science, Kyushu University, Fukuoka, Japan.
Hisakata YamadaDepartment of Clinical Immunology, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan yamada.hisakata.579@m.kyushu-u.ac.jp.ORCID 0000-0002-6329-7222
Masahiro AyanoDepartment of Medicine and Biosystemic Science, Kyushu University, Fukuoka, Japan.
Yasutaka KimotoDepartment of Internal Medicine, Kyushu University Beppu Hospital, Beppu, Japan.
Hiroki MitomaDepartment of Medicine and Biosystemic Science, Kyushu University, Fukuoka, Japan.
Nobuyuki OnoDepartment of Medicine and Biosystemic Science, Kyushu University, Fukuoka, Japan.
Yojiro ArinobuDepartment of Medicine and Biosystemic Science, Kyushu University, Fukuoka, Japan.
Masakazu KondoKondo Clinic for Rheumatology and Orthopaedics, Fukuoka, Japan.
Yasuharu NakashimaDepartment of Orthopedic Surgery, Kyushu University, Fukuoka, Japan.
Koichi AkashiDepartment of Medicine and Biosystemic Science, Kyushu University, Fukuoka, Japan.
Takahiko HoriuchiFukuoka City Hospital, Fukuoka, Japan.
Hiroaki NiiroDepartment of Medical Education, Kyushu University, Fukuoka, Japan.
Kyushu University · JPFukuoka City Hospital · JPKyushu University Beppu Hospital · JPOno Clinic · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesUnderstanding interpatient variation in CD4+T-cell responses is the bases for understanding the pathogenesis and management of rheumatoid arthritis (RA). We examined immune responses to SARS-CoV-2 vaccine in a cohort of patients with RA and determined factors associated with the responses.

methodsFour hundred and thirty-one patients with RA having received two doses of BNT162b2, a messenger RNA-based vaccine for SARS-CoV-2, were included. Vaccine antigen-specific IgG was detected by ELISA, and antigen-specific CD4+T cells were detected by CD154 expression in response to antigenic stimulation. Expression of cytokines was concomitantly detected by intracellular staining. Associations among background variables, antigen-specific antibody production and the CD4+T-cell responses were analysed. Unsupervised hierarchical clustering was performed based on the profiles of antigen-specific cytokine production by CD4+T cells to stratify patients with RA.

resultsMultivariate analysis indicated that ageing negatively affects CD4+T-cell response as well as antibody production. No association was detected between the presence or the levels of rheumatoid factor/anti-cyclic citrullinated peptide antibody and anti-vaccine immune responses. Methotrexate and prednisolone reduced B cell but not T-cell responses. Conventional immunophenotyping by the expression of chemokine receptors was not associated with the actual CD4+T-cell response, except for T helper cells (Th1). Functional immunophenotyping based on the profiles of antigen-specific cytokine production of CD4+T cells stratified patients with RA into three clusters, among which Th1-dominant type less frequently underwent joint surgery.

conclusionsClinical and immunological variables that are associated with antigen-specific CD4 T-cell responses in patients with RA were determined by analysing immune responses against SARS-CoV-2 vaccine.

Indexed as

Arthritis, RheumatoidCD4-Positive T-LymphocytesBNT162 VaccineCOVID-19 VaccinesCytokinesHumansBNT162 VaccineCOVID-19 VaccinesCytokinesArthritis, RheumatoidT-Lymphocyte subsetsVaccination

Identifiers

PMID38216287
PMCPMC10806600
OpenAlexW4390824237

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.