Evidence map›Paper›PMID 30064357›Full record

ArticleBMC infectious diseases2018

MALDI-TOF MS monitoring of PBMC activation status in sepsis.

Aurélie Daumas, Julie Alingrin, Richard Ouedraogo, Patrick Villani, Marc Leone, Jean-Louis Mege

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in BMC infectious diseases, 2018. 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
0.5field-weighted citation impact, top 36% 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, 8 citations in OpenAlex.

  1. 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

6 authors at 4 institutions in 1 country.

Aurélie DaumasAix-Marseille Université, URMITE, IHU Méditerranée Infection, UMR CNR 7278, IRD 198, INSERM 1095, Marseille, France. aurelie.daumas@ap-hm.fr.
Julie AlingrinAix-Marseille Université, URMITE, IHU Méditerranée Infection, UMR CNR 7278, IRD 198, INSERM 1095, Marseille, France.
Richard OuedraogoAix-Marseille Université, URMITE, IHU Méditerranée Infection, UMR CNR 7278, IRD 198, INSERM 1095, Marseille, France.
Patrick VillaniService de Médecine Interne et Thérapeutique, Hôpital de la Timone, Assistance Publique-Hôpitaux de Marseille, Marseille, France.
Marc LeoneAix-Marseille Université, URMITE, IHU Méditerranée Infection, UMR CNR 7278, IRD 198, INSERM 1095, Marseille, France.
Jean-Louis MegeAix-Marseille Université, URMITE, IHU Méditerranée Infection, UMR CNR 7278, IRD 198, INSERM 1095, Marseille, France.
Institut de Recherche pour le Développement · FRMéditerranée Infection Foundation · FRHôpital de la Timone · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMALDI-TOF mass spectrometry (MS) on whole cells enables the detection of different cell types and cell activation. Here, we wondered whether this approach would be useful to investigate the host response in sepsis.

methodsPeripheral blood mononuclear cells (PBMCs) from patients with severe sepsis and healthy donors were analyzed with MALDI-TOF MS. PBMCs from healthy donors were also stimulated with lipopolysaccharide, peptidoglycan, CpG oligonucleotides, polyinosinic polycytidylic acid, and with heat-inactivated bacteria. Averaged spectra of PBMCs stimulated in vitro by different agonists were generated from the database using the Biotyper software and matching scores between each spectrum from patients and averaged spectra from the database were calculated.

resultsWe show that the MALDI-TOF MS signature of PBMCs from septic patients was specific, compared with healthy controls. As the fingerprints observed in patients may be related to PBMC activation, PBMCs from healthy controls were stimulated with cytokines, soluble Pathogen-Associated Molecular Patterns (PAMPs) and heat-killed bacteria, and we created a database of reference spectra. The MALDI-TOF MS profiles of PBMCs from septic patients were then compared with the database. No differences were found between patients with documented infection (n = 6) and those without bacteriological documentation (n = 6). The spectra of PBMCs from septic patients matched with those of interferon-γ- and interleukin-10-stimulated PBMCs, confirming that sepsis is characterized by both inflammatory and immunoregulatory features. Interestingly, the spectra of PBMCs from septic patients without documented infection matched with the reference spectrum of PBMCs stimulated by CpG oligonucleotides, suggesting a bacterial etiology in these patients.

conclusionsDespite the limits of this preliminary study, these results indicate that the monitoring of functional status of PBMCs in peripheral blood by whole cell MALDI-TOF MS could provide unique opportunities to assess disease progression or resolution in clinical settings.

Indexed as

Lymphocyte ActivationSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationAdolescentAdultBacteriaCase-Control StudiesCpG IslandsDisease ProgressionHumansInterferon-gammaInterleukin-10Leukocytes, MononuclearLipopolysaccharidesMonitoring, PhysiologicOligonucleotidesPeptide MappingInterferon-gammaInterleukin-10LipopolysaccharidesOligonucleotidesCpG oligonucleotidesIFN-γInterleukin-10MALDI-TOFMass spectrometryMononuclear cellsSepsis

Identifiers

PMID30064357
PMCPMC6069833
OpenAlexW2887418492

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Registered trials

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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.