Evidence map›Paper›PMID 37540749›Full record

ArticleScience advances2023

Repetitive mRNA vaccination is required to improve the quality of broad-spectrum anti-SARS-CoV-2 antibodies in the absence of CXCL13.

Marne Azarias Da Silva, Pierre Nioche, Calaiselvy Soudaramourty, Anne Bull-Maurer, Mounira Tiouajni, Dechuan Kong, Ouafa Zghidi-Abouzid, Morgane Picard, Ana Mendes-Frias, André Santa-Cruz and 17 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2023. 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
1.2field-weighted citation impact, top 23% 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, 6 citations in OpenAlex.

  1. From Bench to Bedside: Reframing theJournal of clinical & cellular immunology · 2026
    Article
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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

27 authors at 8 institutions in 4 countries.

Marne Azarias Da SilvaINSERM-U1124, Université Paris Cité, Paris, France.ORCID 0009-0006-3411-1835
Pierre NiocheINSERM-U1124, Université Paris Cité, Paris, France.ORCID 0000-0001-7981-9163
Calaiselvy SoudaramourtyINSERM-U1124, Université Paris Cité, Paris, France.
Anne Bull-MaurerUniversité de Tours, INSERM, UMR1259 MAVIVH, Tours, France.
Mounira TiouajniINSERM-U1124, Université Paris Cité, Paris, France.
Dechuan KongJoint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, Japan.ORCID 0000-0003-3779-6666
Ouafa Zghidi-AbouzidCHU de Québec-Université Laval Research Center, Québec City, Québec, Canada.ORCID 0000-0001-8502-4068
Morgane PicardINSERM-U1124, Université Paris Cité, Paris, France.
Ana Mendes-FriasLife and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal.ORCID 0000-0002-7561-5347
André Santa-CruzLife and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal.ORCID 0000-0002-5636-575X
Alexandre CarvalhoLife and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal.ORCID 0000-0001-5683-3181
Carlos CapelaLife and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal.
Jorge PedrosaLife and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal.ORCID 0000-0002-8204-4888
António Gil CastroLife and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal.ORCID 0000-0002-4684-4183
Paul LoubetService des Maladies Infectieuses et Tropicales, CHU de Nîmes, Nîmes, France.
Albert SottoService des Maladies Infectieuses et Tropicales, CHU de Nîmes, Nîmes, France.
Laurent MullerService de Réanimation Chirugicale, CHU de Nîmes, Nîmes, France.
Jean-Yves LefrantService de Réanimation Chirugicale, CHU de Nîmes, Nîmes, France.
Claire RogerService de Réanimation Chirugicale, CHU de Nîmes, Nîmes, France.
Pierre-Géraud ClaretUrgences Médico-Chirugicales Hospitalisation, CHU de Nîmes, Nîmes, France.
Sandra DuvnjakService de Gérontologie et Prévention du Vieillissement, CHU de Nîmes, Nîmes, France.
Tu-Anh TranService de Pédiatrie, CHU de Nîmes, Nîmes, France.ORCID 0000-0001-6587-1876
Kenzo TokunagaDepartment of Pathology, National Institute of Infectious Diseases, Tokyo, Japan.ORCID 0000-0002-2625-5322
Ricardo SilvestreLife and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal.ORCID 0000-0002-9270-2717
Pierre CorbeauInstitut de Génétique Humaine, UMR9002 CNRS-Université de Montpellier, Montpellier, France.
Fabrizio MammanoINSERM-U1124, Université Paris Cité, Paris, France.ORCID 0000-0002-9193-7696
Jérôme EstaquierINSERM-U1124, Université Paris Cité, Paris, France.ORCID 0000-0002-9432-8044
Centre Hospitalier Universitaire de Nîmes · FRInserm · FRUniversity of Minho · PTCentre National de la Recherche Scientifique · FRHospital Braga · PTNational Institute of Infectious Diseases · JPUniversité de Tours · FRUniversité Laval · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the initial spread of severe acute respiratory syndrome coronavirus 2 infection, several viral variants have emerged and represent a major challenge for immune control, particularly in the context of vaccination. We evaluated the quantity, quality, and persistence of immunoglobulin G (IgG) and IgA in individuals who received two or three doses of messenger RNA (mRNA) vaccines, compared with previously infected vaccinated individuals. We show that three doses of mRNA vaccine were required to match the humoral responses of preinfected vaccinees. Given the importance of antibody-dependent cell-mediated immunity against viral infections, we also measured the capacity of IgG to recognize spike variants expressed on the cell surface and found that cross-reactivity was also strongly improved by repeated vaccination. Last, we report low levels of CXCL13, a surrogate marker of germinal center activation and formation, in vaccinees both after two and three doses compared with preinfected individuals, providing a potential explanation for the short duration and low quality of Ig induced.

Indexed as

COVID-19Antibodies, ViralChemokine CXCL13HumansImmunoglobulin GRNA, MessengerVaccinationAntibodies, ViralChemokine CXCL13CXCL13 protein, humanImmunoglobulin GRNA, Messenger

Identifiers

PMID37540749
PMCPMC10403221
OpenAlexW4385565693

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.