Evidence map›Paper›PMID 27729062›Full record

ArticleArthritis research & therapy2016

Screening for peptides targeted to IL-7Rα for molecular imaging of rheumatoid arthritis synovium.

Carmen Burtea, Sophie Laurent, Tuba Sanli, Deborah Fanfone, Aude Devalckeneer, Sébastien Sauvage, Marie-Claire Beckers, Sandrine Rorive, Isabelle Salmon, Luce Vander Elst and 2 more

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2016. 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
1.7field-weighted citation impact, top 16% 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, 13 citations in OpenAlex.

  1. Article
  2. Peptide targeting improves the delivery and therapeutic index of glucocorticoids to treat rheumatoid arthritis.Journal of controlled release : official journal of the Controlled Release Society · 2024
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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

12 authors at 6 institutions in 2 countries.

Carmen BurteaDepartment of General, Organic and Biomedical Chemistry, NMR and Molecular Imaging Laboratory, University of Mons, Avenue Maistriau 19, Mendeleev Building, Mons, B-7000, Belgium. Carmen.Burtea@umons.ac.be.
Sophie LaurentDepartment of General, Organic and Biomedical Chemistry, NMR and Molecular Imaging Laboratory, University of Mons, Avenue Maistriau 19, Mendeleev Building, Mons, B-7000, Belgium.
Tuba SanliDepartment of General, Organic and Biomedical Chemistry, NMR and Molecular Imaging Laboratory, University of Mons, Avenue Maistriau 19, Mendeleev Building, Mons, B-7000, Belgium.
Deborah FanfoneDepartment of General, Organic and Biomedical Chemistry, NMR and Molecular Imaging Laboratory, University of Mons, Avenue Maistriau 19, Mendeleev Building, Mons, B-7000, Belgium.
Aude DevalckeneerDepartment of General, Organic and Biomedical Chemistry, NMR and Molecular Imaging Laboratory, University of Mons, Avenue Maistriau 19, Mendeleev Building, Mons, B-7000, Belgium.
Sébastien SauvageDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles, Route de Lennik 808, Brussels, 1070, Belgium.
Marie-Claire BeckersEurogentec S.A., Liège Science Park, Rue du Bois Saint-Jean 5, Seraing, B-4102, Belgium.
Sandrine RoriveDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles, Route de Lennik 808, Brussels, 1070, Belgium.
Isabelle SalmonDepartment of Pathology, Erasme Hospital, Université Libre de Bruxelles, Route de Lennik 808, Brussels, 1070, Belgium.
Luce Vander ElstDepartment of General, Organic and Biomedical Chemistry, NMR and Molecular Imaging Laboratory, University of Mons, Avenue Maistriau 19, Mendeleev Building, Mons, B-7000, Belgium.
Bernard R LauwerysPôle de pathologies rhumatismales inflammatoires et systémiques, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Avenue Mounier 53, Brussels, 1200, Belgium.
Robert N MullerDepartment of General, Organic and Biomedical Chemistry, NMR and Molecular Imaging Laboratory, University of Mons, Avenue Maistriau 19, Mendeleev Building, Mons, B-7000, Belgium.
University of Mons · BEVIB-UAntwerp Center for Molecular Neurology · BEEurogentec (Belgium) · BEImaging Center · USUCLouvain · BEUniversité Libre de Bruxelles · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterleukin-7 receptor alpha (IL-7Rα) represents a biomarker with potential applications in rheumatoid arthritis (RA) diagnosis and therapy. We have therefore searched by phage display potential IL-7Rα specific peptides with the primary goal being to develop in vivo molecular imaging tools.

methodsIL-7Rα-targeted peptides were searched within a disulfide-constrained combinatorial phage displayed library of random linear heptapeptides. The apparent dissociation constant (K

resultsAfter several steps of phage display and peptide screening, two IL-7Rα-specific heptapeptides (P258 and P725) were selected from the initial library, based on their affinity for the target (extracellular domain of IL-7Rα, which contains a fibronectin type III repeat-like sequence). P258 (a linear peptide obtained by removing the Cys-constraint) had the lowest affinity for fibronectin itself and was therefore proposed for molecular imaging. After grafting to ultra-small superparamagnetic particles of iron oxide (USPIO), P258 produced a strong negative contrast on MRI in mice with collagen-induced arthritis (CIA), even at 2 hours post injection. The co-localization of USPIO-P258 with IL-7Rα-expressing cells in the synovial tissue from CIA mice and its ability to discriminate the level of IL-7R expression and the disease severity confirmed its efficacy as an in vivo IL-7Rα imaging agent. Interestingly, the cyclic peptide (P725), which was less adequate for molecular imaging because of higher affinity for fibronectin, had a strong ability to compete with IL-7 for the IL-7Rα binding sites, making it a potential candidate for blocking applications. Accordingly, P725 prevented the signal transducer and activator of transcription 5 (STAT5) activation induced by IL-7 in ADC-stimulated Jurkat cells.

conclusionsThe two peptides identified in this work demonstrate that IL-7Rα targeting in RA presents potential applications for in vivo molecular imaging and putative blocking purposes.

Indexed as

DextransMagnetite NanoparticlesAnimalsArthritis, ExperimentalArthritis, RheumatoidBiomarkersEnzyme-Linked Immunosorbent AssayFemaleHumansMagnetic Resonance ImagingMaleMiceMice, Inbred DBAMolecular ImagingPeptides, CyclicReceptors, Interleukin-7BiomarkersDextransferumoxtran-10interleukin-7 receptor, alpha chainMagnetite NanoparticlesPeptides, CyclicReceptors, Interleukin-7IL-7 receptorMolecular imagingMRIPeptidesPhage displayRheumatoid arthritisUltra-small superparamagnetic particles of iron oxide

Identifiers

PMID27729062
PMCPMC5059943
OpenAlexW2529913480

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.