Evidence map›Paper›PMID 30139949›Full record

ArticleScientific reports2018

α-Gal on the protein surface affects uptake and degradation in immature monocyte derived dendritic cells.

M Krstić Ristivojević, J Grundström, T A T Tran, D Apostolovic, V Radoi, M Starkhammar, V Vukojević, T Ćirković Veličković, C Hamsten, M van Hage

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  4. Review
  5. Article
  6. Article
  7. Review
  8. Galactose α-1,3-galactose phenotypes: Lessons from various patient populations.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2019
    Review
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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

10 authors at 4 institutions in 3 countries.

M Krstić RistivojevićDepartment of Medicine Solna, Immunology and Allergy Unit, Karolinska Institutet, and University Hospital, Stockholm, Sweden.
J GrundströmDepartment of Medicine Solna, Immunology and Allergy Unit, Karolinska Institutet, and University Hospital, Stockholm, Sweden.
T A T TranDepartment of Medicine Solna, Immunology and Allergy Unit, Karolinska Institutet, and University Hospital, Stockholm, Sweden.
D ApostolovicDepartment of Medicine Solna, Immunology and Allergy Unit, Karolinska Institutet, and University Hospital, Stockholm, Sweden.
V RadoiDepartment of Clinical Neuroscience, Center for Molecular Medicine (CMM), Karolinska Institutet, Stockholm, Sweden.
M StarkhammarDepartment of Internal Medicine, Södersjukhuset, Stockholm, Sweden.
V VukojevićDepartment of Clinical Neuroscience, Center for Molecular Medicine (CMM), Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0003-0873-5653
T Ćirković VeličkovićCenter of Excellence in Molecular Food Sciences, Faculty of Chemistry, University of Belgrade, Belgrade, Serbia.
C HamstenDepartment of Medicine Solna, Immunology and Allergy Unit, Karolinska Institutet, and University Hospital, Stockholm, Sweden.
M van HageDepartment of Medicine Solna, Immunology and Allergy Unit, Karolinska Institutet, and University Hospital, Stockholm, Sweden. Marianne.van.Hage@ki.se.
Karolinska University Hospital · SEKarolinska Institutet · SEStockholm South General Hospital · SEUniversity of Belgrade · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Red meat allergy is characterized by an IgE response against the carbohydrate galactose-α-1,3-galactose (α-Gal), which is abundantly expressed on glycoproteins from non-primate mammals. The mechanisms of how α-Gal is processed and presented to the immune system to initiate an allergic reaction are still unknown. The aim of this study was to reveal whether the presence of α-Gal epitopes on the protein surface influence antigen uptake and processing in immature monocyte-derived dendritic cells (iMDDCs). Immature MDDCs were prepared from healthy blood donors and red meat allergic patients. We found an increased internalization of α-Gal carrying proteins over time in iMDDCs by flow cytometric analysis, which was independent of the donor allergic status. The uptake of α-Gal carrying proteins was significantly higher than the uptake of non-α-Gal carrying proteins. Confocal microscopy revealed α-Gal carrying proteins scattered around the cytoplasm in most iMDDCs while detection of proteins not carrying α-Gal was negligible. Fluorescent detection of protein on SDS-PAGE showed that degradation of α-Gal carrying proteins was slower than degradation of non-α-Gal carrying proteins. Thus, the presence of α-Gal on the protein surface affects both uptake and degradation of the protein, and the results add new knowledge of α-Gal as a clinically relevant food allergen.

Indexed as

AnimalsDendritic CellsElectrophoresis, Polyacrylamide GelFlow CytometryGalactoseGlycoproteinsHumansMicroscopy, ConfocalMonocytesSerum Albumin, BovineGalactoseGlycoproteinsSerum Albumin, Bovine

Identifiers

PMID30139949
PMCPMC6107510
OpenAlexW2886723034

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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.