Evidence map›Paper›PMID 34290706›Full record

ArticleFrontiers in immunology2021

Assessing the Functional Heterogeneity of Monocytes in Human Septic Shock: a Proof-of-Concept Microfluidic Assay of TNFα Secretion.

Jean-François Llitjos, Yacine Bounab, Christophe Rousseau, Sophie Dixneuf, Blandine Rimbault, Jean-Daniel Chiche, Julien Textoris, Frédéric Pène, Christophe Védrine

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Prediction of outcome using CD14Medical microbiology and immunology · 2023
    Article
  4. Article
  5. 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

9 authors at 5 institutions in 1 country.

Jean-François LlitjosInstitut Cochin, U1016, CNRS UMR8104, Paris, France.
Yacine BounabBioassays, Microsystems and Optical Engineering, BIOASTER, Lyon, France.
Christophe RousseauInstitut Cochin, U1016, CNRS UMR8104, Paris, France.
Sophie DixneufBioassays, Microsystems and Optical Engineering, BIOASTER, Lyon, France.
Blandine RimbaultBioassays, Microsystems and Optical Engineering, BIOASTER, Lyon, France.
Jean-Daniel ChicheInstitut Cochin, U1016, CNRS UMR8104, Paris, France.
Julien TextorisEA7426 "Pathophysiology of Injury-induced Immunosuppression", Université Claude Bernard Lyon-1 - HCL- BioMérieux, Lyon, France.
Frédéric PèneInstitut Cochin, U1016, CNRS UMR8104, Paris, France.
Christophe VédrineBioassays, Microsystems and Optical Engineering, BIOASTER, Lyon, France.
BIOASTER · FRHôpital Cochin · FRCentre National de la Recherche Scientifique · FRInstitut Cochin · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: The development of advanced single-cell technologies to decipher inter-cellular heterogeneity has enabled the dynamic assessment of individual cells behavior over time, overcoming the limitation of traditional assays. Here, we evaluated the feasibility of an advanced microfluidic assay combined to fluorescence microscopy to address the behavior of circulating monocytes from septic shock patients. Methods: Seven septic shock patients and ten healthy volunteers were enrolled in the study. Using the proposed microfluidic assay we investigated the production over time of LPS-elicited TNFα by single monocytes encapsulated within droplets. Cellular endocytic activity was assessed by internalization of magnetic nanoparticles. Besides, we assessed HLA-DR membrane expression and LPS-induced TNFα production in monocytes through classical flow cytometry assays. Results: Consistent with the flow cytometry results, the total number of TNFα molecules secreted by encapsulated single monocytes was significantly decreased in septic shock patients compared to healthy donors. TNFα production was dampened as soon as 30 and 60 minutes after LPS stimulation in monocytes from septic patients. Furthermore, the microfluidic assay revealed heterogeneous individual behavior of monocytes from septic shock patients. Of note, monocytes from both healthy donors and patients exhibited similar phagocytic activities over time. Conclusion: The microfluidic assay highlights the functional heterogeneity of monocytes, and provides in-depth resolution in assessing the hallmark monocyte deactivation encountered in post-septic immunosuppression.

Indexed as

AdultAgedAged, 80 and overFemaleFlow CytometryHLA-DR AntigensHumansImmunosuppression TherapyLipopolysaccharidesMaleMicrofluidicsMiddle AgedMonocytesProof of Concept StudyShock, SepticTumor Necrosis Factor-alphaHLA-DR AntigensLipopolysaccharidesTumor Necrosis Factor-alphaimmune suppressionmicrofluidicmonocyteseptic shocktolerance

Identifiers

PMID34290706
PMCPMC8288100
OpenAlexW3185317288

What OpenQuestion holds

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LicenceCC BY
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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.