Evidence map›Paper›PMID 37483614›Full record

ArticleFrontiers in immunology2023

Identification and characterisation of anti-IL-13 inhibitory single domain antibodies provides new insights into receptor selectivity and attractive opportunities for drug discovery.

Kayleigh Walker, Roberta Baravalle, Rachel Holyfield, Jacqueline Kalms, Helena Wright, Chitra Seewooruthun, Frederick W Muskett, Anthony Scott-Tucker, Andy Merritt, Alistair Henry and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. 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
0.2field-weighted citation impact, top 40% 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, 1 citations in OpenAlex.

  1. Article
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

14 authors at 4 institutions in 1 country.

Kayleigh WalkerLeicester Institute of Structural and Chemical Biology, and Department of Molecular and Cell Biology, University of Leicester, Leicester, United Kingdom.
Roberta BaravalleLeicester Institute of Structural and Chemical Biology, and Department of Molecular and Cell Biology, University of Leicester, Leicester, United Kingdom.
Rachel HolyfieldLeicester Institute of Structural and Chemical Biology, and Department of Molecular and Cell Biology, University of Leicester, Leicester, United Kingdom.
Jacqueline KalmsLeicester Institute of Structural and Chemical Biology, and Department of Molecular and Cell Biology, University of Leicester, Leicester, United Kingdom.
Helena WrightLeicester Institute of Structural and Chemical Biology, and Department of Molecular and Cell Biology, University of Leicester, Leicester, United Kingdom.
Chitra SeewooruthunLeicester Institute of Structural and Chemical Biology, and Department of Molecular and Cell Biology, University of Leicester, Leicester, United Kingdom.
Frederick W MuskettLeicester Institute of Structural and Chemical Biology, and Department of Molecular and Cell Biology, University of Leicester, Leicester, United Kingdom.
Anthony Scott-TuckerUCB Biopharma, UCB Pharma, Slough, United Kingdom.
Andy MerrittLifeArc, Centre for Therapeutics Discovery, Stevenage Bioscience Catalyst, Stevenage, United Kingdom.
Alistair HenryUCB Biopharma, UCB Pharma, Slough, United Kingdom.
Alastair D G LawsonUCB Biopharma, UCB Pharma, Slough, United Kingdom.
Gareth HallLeicester Institute of Structural and Chemical Biology, and Department of Molecular and Cell Biology, University of Leicester, Leicester, United Kingdom.
Christine ProsserLeicester Institute of Structural and Chemical Biology, and Department of Molecular and Cell Biology, University of Leicester, Leicester, United Kingdom.
Mark D CarrLeicester Institute of Structural and Chemical Biology, and Department of Molecular and Cell Biology, University of Leicester, Leicester, United Kingdom.
Institute of Structural and Molecular Biology · GBUCB Pharma (United Kingdom) · GBUniversity of Leicester · GBStevenage Bioscience Catalyst · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-13 (IL-13) is a cytokine involved in T-cell immune responses and is a well validated therapeutic target for the treatment of asthma, along with other allergic and inflammatory diseases. IL-13 signals through a ternary signalling complex formed with the receptors IL-13Rα1 and IL-4Rα. This complex is assembled by IL-13 initially binding IL-13Rα1, followed by association of the binary IL-13:IL-13Rα1 complex with IL-4Rα. The receptors are shared with IL-4, but IL-4 initially binds IL-4Rα. Here we report the identification and characterisation of a diverse panel of single-domain antibodies (VHHs) that bind to IL-13 (K

Indexed as

Interleukin-13Single-Domain AntibodiesCytokinesInterleukin-13 Receptor alpha1 SubunitInterleukin-4CytokinesInterleukin-13Interleukin-13 Receptor alpha1 SubunitInterleukin-4Single-Domain Antibodiesallosteric regulationinterleukin-13receptor selectivityreceptor signallingsingle domain antibodiesVHH

Identifiers

PMID37483614
PMCPMC10359924
OpenAlexW4383312799

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.