Evidence map›Paper›PMID 27911216›Full record

ArticlemAbs

Validation of antibody reagents for mucin analysis in chronic inflammatory airway diseases.

Thorsten Krause, Niels Röckendorf, Karoline I Gaede, Katrin Ramaker, Heike Sinnecker, Andreas Frey

Open access · goldAbstract readValidation Study
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 90% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Molecular targets for cystic fibrosis and therapeutic potential of monoclonal antibodies.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2022
    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

6 authors at 2 institutions in 1 country.

Thorsten Krausea Division of Mucosal Immunology & Diagnostics, Priority Area Asthma & Allergy, Research Center Borstel, Leibniz Center for Medicine and Biosciences , Borstel , Germany.
Niels Röckendorfa Division of Mucosal Immunology & Diagnostics, Priority Area Asthma & Allergy, Research Center Borstel, Leibniz Center for Medicine and Biosciences , Borstel , Germany.
Karoline I Gaedeb BioMaterialBank (BMB) North, Research Center Borstel, Leibniz Center for Medicine and Biosciences , Borstel , Germany.
Katrin Ramakera Division of Mucosal Immunology & Diagnostics, Priority Area Asthma & Allergy, Research Center Borstel, Leibniz Center for Medicine and Biosciences , Borstel , Germany.
Heike Sinneckera Division of Mucosal Immunology & Diagnostics, Priority Area Asthma & Allergy, Research Center Borstel, Leibniz Center for Medicine and Biosciences , Borstel , Germany.
Andreas Freya Division of Mucosal Immunology & Diagnostics, Priority Area Asthma & Allergy, Research Center Borstel, Leibniz Center for Medicine and Biosciences , Borstel , Germany.
Research Center Borstel - Leibniz Lung Center · DEGerman Center for Lung Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In chronic inflammatory airway diseases, mucins display disease-related alterations in quantity, composition and glycosylation. This opens the possibility to diagnose and monitor inflammatory airway disorders and their exacerbation based on mucin properties. For such an approach to be reasonably versatile and diagnostically meaningful, the mucin of interest must be captured in a reliable, patient-independent way. To identify appropriate mucin-specific reagents, we tested anti-mucin antibodies on mucin-content-standardized, human bronchoalveolar lavage fluid samples in immunoblot assays. All commercially available monoclonal antibodies against the major airway mucin MUC5AC were screened, except for those with known specificity for carbohydrates, as glycosylation patterns are not mucin-specific. Our results indicated considerable inter-patient and inter-antibody variability in mucin recognition for all antibodies and samples tested. The best results in terms of signal strength and reproducibility were obtained with antibodies Mg-31, O.N.457 and 45M1. Additional epitope mapping experiments revealed that only one of the antibodies with superior binding to MUC5AC recognized linear peptide epitopes on the protein backbone.

Indexed as

Antibodies, MonoclonalAntibody SpecificityAsthmaBronchoalveolar Lavage FluidEpitope MappingEpitopesHumansMucin 5ACAntibodies, MonoclonalEpitopesMUC5AC protein, humanMucin 5ACAsthmachronic inflammatory airway diseasesCOPDMUC5ACmucin capturingmucin quantificationmucus

Identifiers

PMID27911216
PMCPMC5297535
OpenAlexW2558448901

What OpenQuestion holds

Textmetadata
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.