Evidence map›Paper›PMID 21955279›Full record

ArticleScandinavian journal of immunology2012

FluoroSpot Analysis of TLR-Activated Monocytes Reveals Several Distinct Cytokine-Secreting Subpopulations.

C Smedman, T Ernemar, L Gudmundsdotter, P Gille-Johnson, A Somell, K Nihlmark, B Gårdlund, J Andersson, S Paulie

Abstract read
In one paragraph

Article in Scandinavian journal of immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Monocyte Subpopulation Recovery as Predictors of Hematopoietic Cell Transplantation Outcomes.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Article
  9. Role of Monocytes in Heart Failure and Atrial Fibrillation.Journal of the American Heart Association · 2018
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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.

C SmedmanDivision of Infectious Diseases, Department of Medicine, Karolinska Institute, Stockholm, SwedenMabtech AB, Nacka Strand, SwedenDepartment of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden.
T ErnemarDivision of Infectious Diseases, Department of Medicine, Karolinska Institute, Stockholm, SwedenMabtech AB, Nacka Strand, SwedenDepartment of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden.
L GudmundsdotterDivision of Infectious Diseases, Department of Medicine, Karolinska Institute, Stockholm, SwedenMabtech AB, Nacka Strand, SwedenDepartment of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden.
P Gille-JohnsonDivision of Infectious Diseases, Department of Medicine, Karolinska Institute, Stockholm, SwedenMabtech AB, Nacka Strand, SwedenDepartment of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden.
A SomellDivision of Infectious Diseases, Department of Medicine, Karolinska Institute, Stockholm, SwedenMabtech AB, Nacka Strand, SwedenDepartment of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden.
K NihlmarkDivision of Infectious Diseases, Department of Medicine, Karolinska Institute, Stockholm, SwedenMabtech AB, Nacka Strand, SwedenDepartment of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden.
B GårdlundDivision of Infectious Diseases, Department of Medicine, Karolinska Institute, Stockholm, SwedenMabtech AB, Nacka Strand, SwedenDepartment of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden.
J AnderssonDivision of Infectious Diseases, Department of Medicine, Karolinska Institute, Stockholm, SwedenMabtech AB, Nacka Strand, SwedenDepartment of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden.
S PaulieDivision of Infectious Diseases, Department of Medicine, Karolinska Institute, Stockholm, SwedenMabtech AB, Nacka Strand, SwedenDepartment of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monocytes have long been considered a heterogeneous group of cells both in terms of morphology and function. In humans, three distinct subsets have been described based on their differential expression of the cell surface markers CD14 and CD16. However, the relationship between these subsets and the production of cytokines has for the most part been based on ELISA measurements, making it difficult to draw conclusions as to their functional profile on the cellular level. In this study, we have investigated lipoteichoic acid (LTA)- and lipopolysaccharide (LPS)-induced cytokine secretion by monocytes using the FluoroSpot technique. This method measures the number of cytokine-secreting cells on the single-cell level and uses fluorescent detection, allowing for the simultaneous analysis of two cytokines from the same population of isolated cells. By this approach, human monocytes from healthy volunteers could be divided into several subgroups as IL-1β, IL-6, TNF-α and MIP-1β were secreted by larger populations of responding cells (25.9-39.2%) compared with the smaller populations of GM-CSF (9.1%), IL-10 (1.3%) and IL-12p40 (1.2%). Furthermore, when studying co-secretion in FluoroSpot, an intricate relationship between the monocytes secreting IL-1β and/or IL-6 and those secreting TNF-α, MIP-1β, GM-CSF, IL-10 and IL-12p40 was revealed. In this way, dissecting the secretion pattern of the monocytes in response to TLR-2 or TLR-4 stimulation, several subpopulations with distinct cytokine-secreting profiles could be identified.

Indexed as

Cell LineageChemokine CCL4Flow CytometryGene ExpressionGranulocyte-Macrophage Colony-Stimulating FactorHumansInterleukin-10Interleukin-12 Subunit p40Interleukin-1betaInterleukin-6LipopolysaccharidesMonocytesPrimary Cell CultureSingle-Cell AnalysisTeichoic AcidsToll-Like Receptor 2Chemokine CCL4Granulocyte-Macrophage Colony-Stimulating FactorIL10 protein, humanIL6 protein, humanInterleukin-10Interleukin-12 Subunit p40Interleukin-1betaInterleukin-6Lipopolysaccharideslipoteichoic acidTeichoic AcidsTLR2 protein, humanTLR4 protein, humanToll-Like Receptor 2Toll-Like Receptor 4Tumor Necrosis Factor-alpha

Identifiers

PMID21955279
PMCPMC3321223

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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.