Evidence map›Paper›PMID 28736835›Full record

ArticleEuropean journal of immunology2017

Peptide mimetics of immunoglobulin A (IgA) and FcαRI block IgA-induced human neutrophil activation and migration.

Marieke H Heineke, Lydia P E van der Steen, Rianne M Korthouwer, J Joris Hage, Johannes P M Langedijk, Joris J Benschop, Jantine E Bakema, Jerry W Slootstra, Marjolein van Egmond

Open access · hybridAbstract read
In one paragraph

Article in European journal of immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Intrahepatic inflammatory IgAJournal for immunotherapy of cancer · 2022
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Immunoglobulin A Glycosylation and Its Role in Disease.Experientia supplementum (2012) · 2021
    Article
  7. Article
  8. Review
  9. IgA: Structure, Function, and Developability.Antibodies (Basel, Switzerland) · 2019
    Review
  10. Review
  11. 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 at 3 institutions in 1 country.

Marieke H HeinekeDepartment of Molecular Cell Biology and Immunology, VU University Medical Center, Amsterdam, The Netherlands.
Lydia P E van der SteenDepartment of Molecular Cell Biology and Immunology, VU University Medical Center, Amsterdam, The Netherlands.
Rianne M KorthouwerDepartment of Molecular Cell Biology and Immunology, VU University Medical Center, Amsterdam, The Netherlands.
J Joris HageDepartment of Plastic and Reconstructive Surgery, Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Johannes P M LangedijkPepscan Therapeutics, Zuidersluisweg 2, Lelystad, The Netherlands.
Joris J BenschopPepscan Therapeutics, Zuidersluisweg 2, Lelystad, The Netherlands.
Jantine E BakemaDepartment of Otolaryngology/Head-Neck Surgery, VU University Medical Center, Amsterdam, The Netherlands.
Jerry W SlootstraPepscan Therapeutics, Zuidersluisweg 2, Lelystad, The Netherlands.
Marjolein van EgmondDepartment of Molecular Cell Biology and Immunology, VU University Medical Center, Amsterdam, The Netherlands.ORCID 0000-0001-6308-9266
Amsterdam UMC Location Vrije Universiteit Amsterdam · NLPepscan (Netherlands) · NLThe Netherlands Cancer Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cross-linking of the IgA Fc receptor (FcαRI) by IgA induces release of the chemoattractant LTB4, thereby recruiting neutrophils in a positive feedback loop. IgA autoantibodies of patients with autoimmune blistering skin diseases therefore induce massive recruitment of neutrophils, resulting in severe tissue damage. To interfere with neutrophil mobilization and reduce disease morbidity, we developed a panel of specific peptides mimicking either IgA or FcαRI sequences. CLIPS technology was used to stabilize three-dimensional structures and to increase peptides' half-life. IgA and FcαRI peptides reduced phagocytosis of IgA-coated beads, as well as IgA-induced ROS production and neutrophil migration in in vitro and ex vivo (human skin) experiments. Since topical application would be the preferential route of administration, Cetomacrogol cream containing an IgA CLIPS peptide was developed. In the presence of a skin permeation enhancer, peptides in this cream were shown to penetrate the skin, while not diffusing systemically. Finally, epitope mapping was used to discover sequences important for binding between IgA and FcαRI. In conclusion, a cream containing IgA or FcαRI peptide mimetics, which block IgA-induced neutrophil activation and migration in the skin may have therapeutic potential for patients with IgA-mediated blistering skin diseases.

Indexed as

Administration, TopicalAntigens, CDAutoantibodiesAutoimmune DiseasesCetomacrogolEpitope MappingHalf-LifeHumansImmune System DiseasesImmunoglobulin ALeukocyte DisordersLeukotriene B4Neutrophil ActivationNeutrophil InfiltrationNeutrophilsPeptide LibraryAntigens, CDAutoantibodiesCetomacrogolFc(alpha) receptorImmunoglobulin ALeukotriene B4Peptide LibraryPeptidomimeticsReactive Oxygen SpeciesReceptors, FcAutoimmune blistering skin diseaseCD89Epitope mappingFc alpha receptorImmunoglobulin ANeutrophilPeptide mimetic

Identifiers

PMID28736835
PMCPMC5659136
OpenAlexW2738327007

What OpenQuestion holds

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LicenceCC BY
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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.