Evidence map›Paper›PMID 30326568›Full record

ArticleInternational journal of molecular sciences2018

Allergen Delivery Inhibitors: Characterisation of Potent and Selective Inhibitors of Der p 1 and Their Attenuation of Airway Responses to House Dust Mite Allergens.

Jihui Zhang, Jie Chen, Jie Zuo, Gary K Newton, Mark R Stewart, Trevor R Perrior, David R Garrod, Clive Robinson

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Jihui ZhangInstitute for Infection & Immunity, St George's, University of London, Cranmer Terrace, London SW17 0RE, UK. zhang.jihui@im.ac.cn.
Jie ChenInstitute for Infection & Immunity, St George's, University of London, Cranmer Terrace, London SW17 0RE, UK. jchen99556688@outlook.com.
Jie ZuoInstitute for Infection & Immunity, St George's, University of London, Cranmer Terrace, London SW17 0RE, UK. mrzuojie@126.com.
Gary K NewtonDomainex Ltd., Chesterford Research Park, Little Chesterford, Saffron Walden, Essex CB10 1XL, UK. Gary.Newton@domainex.co.uk.
Mark R StewartDomainex Ltd., Chesterford Research Park, Little Chesterford, Saffron Walden, Essex CB10 1XL, UK. Mark.Stewart@domainex.co.uk.
Trevor R PerriorDomainex Ltd., Chesterford Research Park, Little Chesterford, Saffron Walden, Essex CB10 1XL, UK. Trevor.Perrior@domainex.co.uk.
David R GarrodFaculty of Biology Medicine and Health, University of Manchester, Manchester M13 9PL, UK. d.garrod@manchester.ac.uk.
Clive RobinsonInstitute for Infection & Immunity, St George's, University of London, Cranmer Terrace, London SW17 0RE, UK. c.robinson@sgul.ac.uk.ORCID 0000-0001-6253-7864
St George's, University of London · GBDomainex (United Kingdom) · GBUniversity of Manchester · GB

Funding

Wellcome Trust 087650
6 · The paper itself

Abstract

Group 1 allergens of house dust mites (HDM) are globally significant triggers of allergic disease. They are considered as initiator allergens because their protease activity enables the development of allergy to a spectrum of unrelated allergens from various sources. This initiator-perpetuator function identifies Group 1 HDM allergens as attractive drug design targets for the first small-molecule approach directed towards a non-human, root cause trigger of allergic disease. The purpose of this study was to: (i) identify exemplar inhibitors of these allergens using Der p 1 as a design template, and (ii) characterise the pharmacological profiles of these compounds using in vitro and in vivo models relevant to allergy. Potent inhibitors representing four different chemotypes and differentiated by mechanism of action were investigated. These compounds prevented the ab initio development of allergy to the full spectrum of HDM allergens and in established allergy they inhibited the recruitment of inflammatory cells and blunted acute allergic bronchoconstriction following aerosol challenge with the full HDM allergen repertoire. Collectively, the data obtained in these experiments demonstrate that the selective pharmacological targeting of Der p 1 achieves an attractive range of benefits against exposure to all HDM allergens, consistent with the initiator-perpetuator function of this allergen.

Indexed as

Amino Acid SequenceAnimalsAnti-Allergic AgentsAntigens, DermatophagoidesArthropod ProteinsCysteine EndopeptidasesCytokinesDisease Models, AnimalDrug DesignHumansHypersensitivityImmunomodulationKineticsMiceProteolysisRespiratory Function TestsAnti-Allergic AgentsAntigens, DermatophagoidesArthropod ProteinsCysteine EndopeptidasesCytokinesDermatophagoides pteronyssinus antigen p 1airway inflammationallergen delivery inhibitorallergensDer p 1eosinophilhouse dust mite

Identifiers

PMID30326568
PMCPMC6214017
OpenAlexW2896759018

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.