Evidence map›Paper›PMID 40986015›Full record

ArticleIntensive care medicine2025

Monocyte HLA-DR expression in septic shock patients: insights from a 20-year real-world cohort of 1023 cases.

Guillaume Monneret, Thomas Lafon, Morgane Gossez, Bruno Evrard, Maxime Bodinier, Thomas Rimmelé, Laurent Argaud, Martin Cour, Arnaud Friggeri, Alain Lepape and 3 more

Erratum issuedAbstract read
In one paragraph

Article in Intensive care medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

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  18. Parallel single-cell host immune profiling and pathogen genomic characterization inFrontiers in cellular and infection microbiology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Guillaume Monneret *Hospices Civils de Lyon, Immunology Laboratory, Hôpital E. Herriot, Lyon, France. Guillaume.monneret@chu-lyon.fr.ORCID 0000-0002-9961-5739
Thomas Lafon *Hospices Civils de Lyon, Immunology Laboratory, Hôpital E. Herriot, Lyon, France.
Morgane GossezHospices Civils de Lyon, Immunology Laboratory, Hôpital E. Herriot, Lyon, France.
Bruno EvrardIntensive Care Medicine Department, Limoges University Hospital, Limoges, France.
Maxime BodinierResearch and Development Department, bioMérieux S.A, Marcy l'Etoile, France.
Thomas RimmeléHospices Civils de Lyon, Anesthesiology and Critical Care Medicine Department, Hôpital E. Herriot, Lyon, France.
Laurent ArgaudHospices Civils de Lyon, Intensive Care Medicine Department, Hôpital E. Herriot, Lyon, France.
Martin CourHospices Civils de Lyon, Intensive Care Medicine Department, Hôpital E. Herriot, Lyon, France.
Arnaud FriggeriHospices Civils de Lyon, Anesthesiology and Critical Care Medicine Department, CH Lyon-Sud, Pierre-Bénite, France.
Alain LepapeHospices Civils de Lyon, Anesthesiology and Critical Care Medicine Department, CH Lyon-Sud, Pierre-Bénite, France.
Bernard AllaouchicheHospices Civils de Lyon, Anesthesiology and Critical Care Medicine Department, CH Lyon-Sud, Pierre-Bénite, France.
Anne-Claire LukaszewiczHospices Civils de Lyon, Anesthesiology and Critical Care Medicine Department, Hôpital E. Herriot, Lyon, France.
Fabienne VenetHospices Civils de Lyon, Immunology Laboratory, Hôpital E. Herriot, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSeptic patients simultaneously experience hyperinflammation and immunosuppression, the latter driving ICU-acquired infections, prolonged stays in ICU, and increased mortality. As immunostimulant therapies enter clinical trials, effective stratification is critical to identify patients with the most profound immune dysfunction. Monocyte HLA-DR expression (mHLA-DR) has emerged as the most reliable and actionable biomarker of sepsis-induced immunosuppression.

methodsWe conducted a real-world, 20-year cohort study of 1023 septic shock patients, measuring mHLA-DR by standardized flow cytometry during the first week of ICU admission. Primary outcomes included day-28 and day-90 mortality, and ICU-acquired infections.

resultsLow mHLA-DR (< 8000 AB/C, a threshold already used in phase II trials) was significantly associated with increased mortality and ICU-acquired infections. This association held across static and dynamic measures, multivariate analyses, Kaplan-Meier survival curves, and trajectory clustering (K-means).

conclusionsThis large real-world study confirms that mHLA-DR is a robust enrichment biomarker for identifying the most immunosuppressed septic shock patients at higher risk of adverse outcomes. Importantly, time-course analysis suggests that early immune downregulation may represent a physiological adaptation, while delayed and persistent immunosuppression is associated with worse outcomes. Early single time-point measurements may fail to identify patients who are unlikely to develop delayed immunosuppression. Tracking mHLA-DR trajectories after the initial ICU days is essential for detecting persistent immune dysfunction and selecting patients in case of immunostimulant approaches.

Indexed as

HLA-DR AntigensMonocytesShock, SepticAgedBiomarkersCohort StudiesCross InfectionFemaleFlow CytometryHumansIntensive Care UnitsMaleMiddle AgedBiomarkersHLA-DR AntigensHLA-DRImmunosuppressionMonocyteSepsisSeptic shock

Identifiers

PMID40986015
PMCPMC12504386

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LicenceCC BY-NC
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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.