Evidence map›Paper›PMID 27324828›Full record

ArticleProteomics2016

Adaptive immune response to lipoproteins of Staphylococcus aureus in healthy subjects.

Chi Hai Vu, Julia Kolata, Sebastian Stentzel, Anica Beyer, Manuela Gesell Salazar, Leif Steil, Jan Pané-Farré, Vanessa Rühmling, Susanne Engelmann, Friedrich Götz and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Proteomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Spectral Library Based Analysis of Arginine Phosphorylations inMolecular & cellular proteomics : MCP · 2018
    Article
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 2 countries.

Chi Hai VuInstitute of Immunology and Transfusion Medicine, University Medicine Greifswald, Greifswald, Germany.
Julia KolataInstitute of Immunology and Transfusion Medicine, University Medicine Greifswald, Greifswald, Germany.
Sebastian StentzelInstitute of Immunology and Transfusion Medicine, University Medicine Greifswald, Greifswald, Germany.
Anica BeyerInstitute of Microbiology, University of Greifswald, Greifswald, Germany.
Manuela Gesell SalazarInterfaculty Institute of Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.
Leif SteilInterfaculty Institute of Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.
Jan Pané-FarréInstitute of Microbiology, University of Greifswald, Greifswald, Germany.
Vanessa RühmlingInstitute of Microbiology, University of Greifswald, Greifswald, Germany.
Susanne EngelmannInstitute of Microbiology, University of Greifswald, Greifswald, Germany.
Friedrich GötzDepartment of Microbial Genetics, University of Tübingen, Tübingen, Germany.
Jan Maarten van DijlDepartment of Medical Microbiology, University Medical Center Groningen, Groningen, The Netherlands.
Michael HeckerInstitute of Microbiology, University of Greifswald, Greifswald, Germany.
Ulrike MäderInterfaculty Institute of Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.
Frank SchmidtInterfaculty Institute of Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.
Uwe VölkerInterfaculty Institute of Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.
Barbara M BrökerInstitute of Immunology and Transfusion Medicine, University Medicine Greifswald, Greifswald, Germany. broeker@uni-greifswald.de.
Universität Greifswald · DEUniversitätsmedizin Greifswald · DEHelmholtz Centre for Infection Research · DEUniversity Medical Center Groningen · NLUniversity Medical Center Utrecht · NLUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Staphylococcus aureus is a frequent commensal but also a dangerous pathogen, causing many forms of infection ranging from mild to life-threatening conditions. Among its virulence factors are lipoproteins, which are anchored in the bacterial cell membrane. Lipoproteins perform various functions in colonization, immune evasion, and immunomodulation. These proteins are potent activators of innate immune receptors termed Toll-like receptors 2 and 6. This study addressed the specific B-cell and T-cell responses directed to lipoproteins in human S. aureus carriers and non-carriers. 2D immune proteomics and ELISA approaches revealed that titers of antibodies (IgG) binding to S. aureus lipoproteins were very low. Proliferation assays and cytokine profiling data showed only subtle responses of T cells; some lipoproteins did not elicit proliferation. Hence, the robust activation of the innate immune system by S. aureus lipoproteins does not translate into a strong adaptive immune response. Reasons for this may include inaccessibility of lipoproteins for B cells as well as ineffective processing and presentation of the antigens to T cells.

Indexed as

Adaptive ImmunityAdultBacterial ProteinsB-LymphocytesCells, CulturedCytokinesFemaleGene Expression RegulationHealthy VolunteersHumansImmunoglobulin GLipoproteinsMaleMiddle AgedProteomeProteomicsBacterial ProteinsCytokinesImmunoglobulin GLipoproteinsProteomeVirulence FactorsAntibodyHumanLipoproteinMicrobiologyS. aureusT cell

Identifiers

PMID27324828
PMCPMC5096053
OpenAlexW2469895540

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.