Evidence map›Paper›PMID 35218998›Full record

ArticleTransplantation and cellular therapy2022

B Cell Aplasia Is the Most Powerful Predictive Marker for Poor Humoral Response after BNT162b2 mRNA SARS-CoV-2 Vaccination in Recipients of Allogeneic Hematopoietic Stem Cell Transplantation.

Maxime Jullien, Amandine Le Bourgeois, Marianne Coste-Burel, Pierre Peterlin, Alice Garnier, Marie Rimbert, Berthe-Marie Imbert, Steven Le Gouill, Philippe Moreau, Beatrice Mahe and 10 more

Open access · greenAbstract read
In one paragraph

Article in Transplantation and cellular therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

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  2. Pooled it
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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

20 authors at 2 institutions in 1 country.

Maxime JullienHematology Department, Nantes University Hospital, Nantes, France.
Amandine Le BourgeoisHematology Department, Nantes University Hospital, Nantes, France.
Marianne Coste-BurelVirology Department, Nantes University Hospital, Nantes, France.
Pierre PeterlinHematology Department, Nantes University Hospital, Nantes, France.
Alice GarnierHematology Department, Nantes University Hospital, Nantes, France.
Marie RimbertImmunology Department, Nantes University Hospital, Nantes, France.
Berthe-Marie ImbertVirology Department, Nantes University Hospital, Nantes, France.
Steven Le GouillHematology Department, Nantes University Hospital, Nantes, France.
Philippe MoreauHematology Department, Nantes University Hospital, Nantes, France.
Beatrice MaheHematology Department, Nantes University Hospital, Nantes, France.
Viviane DubruilleHematology Department, Nantes University Hospital, Nantes, France.
Nicolas BlinHematology Department, Nantes University Hospital, Nantes, France.
Anne LokHematology Department, Nantes University Hospital, Nantes, France.
Cyrille TouzeauHematology Department, Nantes University Hospital, Nantes, France.
Thomas GastinneHematology Department, Nantes University Hospital, Nantes, France.
Benoit TessoulinHematology Department, Nantes University Hospital, Nantes, France.
Sophie VantyghemHematology Department, Nantes University Hospital, Nantes, France.
Marie C BénéINSERM UMR1232, CRCINA IRS-UN, University of Nantes, University Hospital, Nantes, France; Hematology Biology Department, Nantes University Hospital, Nantes, France.
Thierry GuillaumeHematology Department, Nantes University Hospital, Nantes, France; INSERM UMR1232, CRCINA IRS-UN, University of Nantes, University Hospital, Nantes, France.
Patrice ChevallierHematology Department, Nantes University Hospital, Nantes, France; INSERM UMR1232, CRCINA IRS-UN, University of Nantes, University Hospital, Nantes, France. Electronic address: patrice.chevallier@chu-nantes.fr.
Nantes Université · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Little is known about the immune response to SARS-CoV-2 vaccination in recipients of allogeneic hematopoietic stem cell transplantation (allo-HSCT). However, several studies have reported that adequate protection could be provided to this population. The purpose of this study was to evaluate which factors can predict the efficacy of SARS-CoV-2 vaccination in these specifically immunosuppressed patients. Specific anti-Spike (S) antibody responses were assessed in a cohort of 117 allo-HSCT recipients after 2 injections of BNT162b2 mRNA SARS-CoV-2 vaccine (V1 and V2). Factors considered liable to influence the antibody response and analyzed in this series were the interval between allo-HSCT and V1, donor source, recipient and donor age, current immunosuppressive/chemotherapy (I/C) treatment, and levels of CD4

Indexed as

COVID-19Hematopoietic Stem Cell TransplantationBiomarkersBNT162 VaccineCD8-Positive T-LymphocytesCOVID-19 VaccinesHumansRNA, MessengerSARS-CoV-2VaccinationBiomarkersBNT162 VaccineCOVID-19 VaccinesRNA, MessengerAllogeneicB cellBNT162b2COVID-19Immune statusLymphopeniaSARS-CoV-2 mRNAVaccine

Identifiers

PMID35218998
PMCPMC8865956
OpenAlexW4213454641

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.