Evidence map›Paper›PMID 33178207›Full record

Trial reportFrontiers in immunology

A Longitudinal Study of Immune Cells in Severe COVID-19 Patients.

Didier Payen, Maxime Cravat, Hadil Maadadi, Carole Didelot, Lydia Prosic, Claire Dupuis, Marie-Reine Losser, Marcelo De Carvalho Bittencourt

Registry-linked trialOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in Frontiers in immunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04386395 (Whole Blood Immune Cells Characterization in Critically Ill COVID-19 Patients), which is not on this map. Cited by 46 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 9% 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.

NCT04386395 completednot on this map

Whole Blood Immune Cells Characterization in Critically Ill COVID-19 Patients: A Prospective Study

TypeobservationalSponsorCentral Hospital, Nancy, FranceRan2020 to 2021Enrolled50ConditionsSARS-CoV-2, Immune System Disorder
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 2 syntheses or guidelines pooled it, 73 citations in OpenAlex.

  1. Pooled it
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  3. Trial
  4. Induction of dysfunctional CD14Frontiers in immunology · 2026
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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

8 authors at 4 institutions in 1 country.

Didier PayenUniversité Paris 7 Denis Diderot, UMR 1160 INSERM, Paris, France.
Maxime CravatUniversité de Lorraine, CHRU-Nancy, Laboratoire d'Immunologie, Nancy, France.
Hadil MaadadiUniversité de Lorraine, CHRU-Nancy, Département d'Anesthésie Réanimation Brabois Adulte, Nancy, France.
Carole DidelotCHRU-Nancy, Plateforme de Cytométrie en Flux Diagnostique, Nancy, France.
Lydia ProsicCHRU-Nancy, Plateforme de Cytométrie en Flux Diagnostique, Nancy, France.
Claire DupuisService de Médecine Intensive et Réanimation, CHU de Clermont-Ferrand, Clermont-Ferrand, France.
Marie-Reine LosserUniversité de Lorraine, CHRU-Nancy, Département d'Anesthésie Réanimation Brabois Adulte, Nancy, France.
Marcelo De Carvalho BittencourtUniversité de Lorraine, CHRU-Nancy, Laboratoire d'Immunologie, Nancy, France.
Inserm · FRUniversité de Lorraine · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Little is known about the time-dependent immune responses in severe COVID-19. Data of 15 consecutive patients were sequentially recorded from intensive care unit admission. Lymphocyte subsets and total monocyte and subsets counts were monitored as well as the expression of HLA-DR. For 5 patients, SARS-CoV-2-specific T-cell polyfunctionality was assessed against Spike and Nucleoprotein SARS-CoV-2 peptides. Non-specific inflammation markers were increased in all patients. Median monocyte HLA-DR expression was below the 8,000 AB/C threshold defining acquired immunodepression. A "V" trend curve for lymphopenia, monocyte numbers, and HLA-DR expression was observed with a nadir between days 11 and 14 after symptoms' onset. Intermediate CD14 CLINICAL

trial registrationhttps://clinicaltrials.gov/, identifier NCT04386395.

Indexed as

Severity of Illness IndexAgedBiomarkersCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCOVID-19FemaleGPI-Linked ProteinsHLA-DR AntigensHumansImmunity, CellularLipopolysaccharide ReceptorsLongitudinal StudiesMaleMiddle AgedMonocytesBiomarkersCD14 protein, humanFCGR3B protein, humanGPI-Linked ProteinsHLA-DR AntigensLipopolysaccharide ReceptorsReceptors, IgGantigen-specific polyfunctional T-cellsimmunityintensive care unitmonocyte HLA-DRSARS-CoV-2

Identifiers

PMID33178207
PMCPMC7597438
OpenAlexW3094602563

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.