Evidence map›Paper›PMID 39066424›Full record

ArticleVaccines2024

Humoral and Cellular Response Induced by Primary Series and Booster Doses of mRNA Coronavirus Disease 2019 Vaccine in Patients with Cardiovascular Disease: A Longitudinal Study.

Yuya Ishihara, Hiroyuki Naruse, Hidetsugu Fujigaki, Reiko Murakami, Tatsuya Ando, Kouhei Sakurai, Komei Uehara, Koki Shimomae, Eirin Sakaguchi, Hidekazu Hattori and 6 more

Abstract read
In one paragraph

Article in Vaccines, 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
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.

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

16 authors.

Yuya IshiharaDepartment of Clinical Laboratory, Fujita Health University Hospital, Toyoake 470-1192, Japan.ORCID 0000-0002-8066-7344
Hiroyuki NaruseDepartment of Clinical Pathophysiology, Fujita Health University Graduate School of Health Sciences, Toyoake 470-1192, Japan.
Hidetsugu FujigakiDepartment of Advanced Diagnostic System Development, Fujita Health University Graduate School of Health Sciences, Toyoake 470-1192, Japan.
Reiko MurakamiInstitute for Glyco-Core Research, Gifu University, Yanagido, Gifu 501-1193, Japan.
Tatsuya AndoDepartment of Joint Research Laboratory of Clinical Medicine, Fujita Health University School of Medicine, Toyoake 470-1192, Japan.
Kouhei SakuraiDepartment of Joint Research Laboratory of Clinical Medicine, Fujita Health University School of Medicine, Toyoake 470-1192, Japan.ORCID 0000-0003-2428-0310
Komei UeharaDepartment of Preventive Medical Sciences, Fujita Health University Graduate of Health Sciences, Toyoake 470-1192, Japan.
Koki ShimomaeDepartment of Preventive Medical Sciences, Fujita Health University Graduate of Health Sciences, Toyoake 470-1192, Japan.
Eirin SakaguchiDepartment of Clinical Pathophysiology, Fujita Health University Graduate School of Health Sciences, Toyoake 470-1192, Japan.
Hidekazu HattoriDepartment of Clinical Pathophysiology, Fujita Health University Graduate School of Health Sciences, Toyoake 470-1192, Japan.
Masayoshi SaraiDepartment of Cardiology, Fujita Health University School of Medicine, Toyoake 470-1192, Japan.ORCID 0000-0001-6621-4325
Junnichi IshiiDepartment of Cardiology, Fujita Health University School of Medicine, Toyoake 470-1192, Japan.
Ryosuke FujiiDepartment of Medical Sciences, Fujita Health University School of Medicine, Toyoake 470-1192, Japan.
Hiroyasu ItoDepartment of Joint Research Laboratory of Clinical Medicine, Fujita Health University School of Medicine, Toyoake 470-1192, Japan.
Kuniaki SaitoDepartment of Advanced Diagnostic System Development, Fujita Health University Graduate School of Health Sciences, Toyoake 470-1192, Japan.
Hideo IzawaDepartment of Cardiology, Fujita Health University School of Medicine, Toyoake 470-1192, Japan.ORCID 0000-0003-2136-2855

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preexisting cardiovascular disease (CVD) is a pivotal risk factor for severe coronavirus disease 2019 (COVID-19). We investigated the longitudinal (over 1 year and 9 months) humoral and cellular responses to primary series and booster doses of mRNA COVID-19 vaccines in patients with CVD. Twenty-six patients with CVD who received monovalent mRNA COVID-19 vaccines were enrolled in this study. Peripheral blood samples were serially drawn nine times from each patient. IgG against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike receptor-binding domain (RBD) was measured using an enzyme-linked immunosorbent assay. The numbers of interferon-γ-releasing cells in response to SARS-CoV-2 peptides were measured using an enzyme-linked immunospot assay. The RBD-IgG titers increased 2 weeks after the primary series and booster vaccination and waned 6 months after vaccination. The S1-specific T cell responses in patients aged < 75 years were favorable before and after booster doses; however, the Omicron BA.1-specific T cell responses were poor. These results suggest that regular vaccination is useful to maintain long-term antibody levels and has implications for booster dose strategies in patients with CVD. Additional booster doses, including Omicron variant-adapted mRNA vaccines, may be recommended for patients with CVD, regardless of age.

Indexed as

cardiovascular diseasehumoral and cellular responselongitudinal studymRNA COVID-19 vaccine

Identifiers

PMID39066424
PMCPMC11281625

What Socratic 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 Socratic graph.