Evidence map›Paper›PMID 31024538›Full record

ArticleFrontiers in immunology2019

BET Bromodomain Inhibitor iBET151 Impedes Human ILC2 Activation and Prevents Experimental Allergic Lung Inflammation.

Bernhard Kerscher, Jillian L Barlow, Batika M Rana, Helen E Jolin, Mayuri Gogoi, Michelle A Bartholomew, Deepali Jhamb, Ashutosh Pandey, David F Tough, Antoon J M van Oosterhout and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-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

15 citing papers in PubMed, 21 citations in OpenAlex.

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  13. Airway hyperresponsiveness development and the toxicity of PM2.5.Environmental science and pollution research international · 2021
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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

11 authors at 3 institutions in 1 country.

Bernhard KerscherMedical Research Council, Laboratory of Molecular Biology, Cambridge, United Kingdom.
Jillian L BarlowMedical Research Council, Laboratory of Molecular Biology, Cambridge, United Kingdom.
Batika M RanaMedical Research Council, Laboratory of Molecular Biology, Cambridge, United Kingdom.
Helen E JolinMedical Research Council, Laboratory of Molecular Biology, Cambridge, United Kingdom.
Mayuri GogoiMedical Research Council, Laboratory of Molecular Biology, Cambridge, United Kingdom.
Michelle A BartholomewAllergic Inflammation DPU, Respiratory Therapy Area, GlaxoSmithKline, Medicines Research Centre, Stevenage, United Kingdom.
Deepali JhambComputational Biology, GSK R&D, Collegeville, PA, United States.
Ashutosh PandeyComputational Biology, GSK R&D, Collegeville, PA, United States.
David F ToughEpigenetics DPU, Immunoinflammation Therapy Area Unit, Glaxo Smith Kline, Medicines Research Centre, Stevenage, United Kingdom.
Antoon J M van OosterhoutAllergic Inflammation DPU, Respiratory Therapy Area, GlaxoSmithKline, Medicines Research Centre, Stevenage, United Kingdom.
Andrew N J McKenzieMedical Research Council, Laboratory of Molecular Biology, Cambridge, United Kingdom.
MRC Laboratory of Molecular Biology · GBGlaxoSmithKline (United Kingdom) · GBMedical Research Council · GB

Funding

Medical Research Council MC_U105178805Medical Research Council U105178805
6 · The paper itself

Abstract

Group 2 innate lymphoid cells (ILC2) increase in frequency in eczema and allergic asthma patients, and thus represent a new therapeutic target cell for type-2 immune-mediated disease. The bromodomain and extra-terminal (BET) protein family of epigenetic regulators are known to support the expression of cell cycle and pro-inflammatory genes during type-1 inflammation, but have not been evaluated in type-2 immune responses. We isolated human ILC2 and examined the capacity of the BET protein inhibitor, iBET151, to modulate human ILC2 activation following IL-33 stimulation. iBET151 profoundly blocked expression of genes critical for type-2 immunity, including type-2 cytokines, cell surface receptors and transcriptional regulators of ILC2 differentiation and activation. Furthermore,

Indexed as

AllergensAnimalsAnti-Inflammatory AgentsAsthmaBromodomain Containing ProteinsCytokinesHumansHypersensitivityImmunity, InnateLungLymphocytesMicePneumoniaProteinsAllergensAnti-Inflammatory Agentsbromodomain and extra-terminal domain protein, humanBromodomain Containing ProteinsCytokinesProteinsallergyasthmabromodomainextra-terminal motif proteinILC2Th2

Identifiers

PMID31024538
PMCPMC6465521
OpenAlexW2935913412

What OpenQuestion 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 OpenQuestion graph.