Evidence map›Paper›PMID 36403401›Full record

ArticleJournal of infection and public health2022

De novo natural anti-M alloantibody emergence in severe Coronavirus Disease 2019.

Robin Jeannet, Alexandra Descazeaud, Thomas Daix, Hélène Pauthier, Virginie Pascal, Sébastien Hantz, Sophie Le Cam, Bruno Francois, Jean Feuillard, Xavier Lafarge

Open access · goldAbstract read
In one paragraph

Article in Journal of infection and public health, 2022. 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
0.6field-weighted citation impact, top 28% 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, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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

10 authors at 4 institutions in 1 country.

Robin JeannetINSERM CIC 1435, CHU Dupuytren, and UMR CNRS 7276 INSERM 1262, Université de Limoges, Limoges, France. Electronic address: Robin.jeannet@unilim.fr.
Alexandra DescazeaudLaboratoire d'Immunohématologie, Établissement Français du Sang Nouvelle-Aquitaine, Limoges, France. Electronic address: Alexandra.Descazeaud@efs.sante.fr.
Thomas DaixINSERM CIC 1435 and Réanimation polyvalente, CHU Dupuytren, and INSERM UMR 1092, Université de Limoges, Limoges, France. Electronic address: thomas.daix@chu-limoges.fr.
Hélène PauthierLaboratoire d'Immunohématologie, Établissement Français du Sang Nouvelle-Aquitaine, Limoges, France. Electronic address: Helene.Pauthier@efs.sante.fr.
Virginie PascalUMR CNRS 7276, INSERM 1262, Université de Limoges, and Laboratoire d'Immunologie, CHU Dupuytren, Limoges, France. Electronic address: Virginie.PASCAL@chu-limoges.fr.
Sébastien HantzUMR INSERM 1092, RESINFIT, Université de Limoges, and Centre National de Référence des Herpèsvirus and Service de Bactériologie, Virologie et Hygiène, CHU Dupuytren, Limoges, France. Electronic address: Sebastien.Hantz@chu-limoges.fr.
Sophie Le CamLaboratoire de qualification biologique des dons, Établissement Français du Sang Centre-Pays de la Loire, Angers, France. Electronic address: sophie.lecam@efs.sante.fr.
Bruno FrancoisINSERM CIC 1435 and Réanimation polyvalente, CHU Dupuytren, and INSERM UMR 1092, Université de Limoges, Limoges, France. Electronic address: b.francois@unilim.fr.
Jean FeuillardUMR CNRS 7276 / INSERM 1262 CRIBL and Laboratoire d'Hématologie, Faculté de Médecine and CHU Dupuytren, Limoges, France. Electronic address: jean.feuillard@unilim.fr.
Xavier LafargeINSERM U1035 Biothérapie des Maladies Génétiques, Inflammatoires et Cancers, and Direction Médicale, Établissement Français du Sang Nouvelle-Aquitaine, Bordeaux, France. Electronic address: xavier.lafarge@efs.sante.fr.
Inserm · FRCentre National de la Recherche Scientifique · FRHôpital Pellegrin · FRCentre Pays de la Loire · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The immune response is a key player in the course of SARS-CoV-2 infection, and is often seriously dysfunctional in severe Coronavirus Disease 2019. The hyperinflammatory status has been described to be accompanied by the appearance of autoantibodies. In a lethal COVID-19 infection, we observed the emergence of a de novo natural alloantibody which targeted the M antigen from the MNS blood group on red blood cells (RBC) without evidence of any cross-reaction with SARS-CoV-2 antigens. This IgM lambda alloantibody was unmutated and unswitched. Here, we describe for the first time the emergence of a bystander de novo natural alloantibody against RBCs in a severe COVID-19 patient, highlighting the extra-follicular humoral response reported in these cases.

Indexed as

Blood Group AntigensCOVID-19ErythrocytesHumansSARS-CoV-2Blood Group AntigensAlloantibodyCOVID-19M-antigenTransfusion

Identifiers

PMID36403401
PMCPMC9628129
OpenAlexW4308149123

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.