Evidence map›Paper›PMID 36439637›Full record

ArticleClinical & translational immunology2022

A peptoid interleukin-15 receptor antagonist suppresses inflammation and arthritis in mice.

Kwang Bog Cho, Satya Prakash Shukla, Maheshkumar Kannan, Haowen Zhang, Sundus Jabeen Amina, Shuang Zhou, Yanping Chen, Jeremiah F Molligan, Veena Taneja, Chandra Mohan and 2 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2022. 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
0.4field-weighted citation impact, top 41% 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, 7 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

12 authors at 3 institutions in 1 country.

Kwang Bog ChoDepartment of Pharmacological and Pharmaceutical Sciences University of Houston Houston TX USA.
Satya Prakash ShuklaDepartment of Pharmacological and Pharmaceutical Sciences University of Houston Houston TX USA.
Maheshkumar KannanDepartment of Pharmacological and Pharmaceutical Sciences University of Houston Houston TX USA.
Haowen ZhangDepartment of Pharmacological and Pharmaceutical Sciences University of Houston Houston TX USA.
Sundus Jabeen AminaDepartment of Pharmacological and Pharmaceutical Sciences University of Houston Houston TX USA.
Shuang ZhouDepartment of Pharmacological and Pharmaceutical Sciences University of Houston Houston TX USA.
Yanping ChenDepartment of Biomedical Engineering University of Houston Houston TX USA.
Jeremiah F MolliganDepartment of Anatomic Pathology Mayo Clinic Rochester MN USA.
Veena TanejaDepartment of Immunology and Rheumatology Mayo Clinic Rochester MN USA.
Chandra MohanDepartment of Biomedical Engineering University of Houston Houston TX USA.
D Gomika UdugamasooriyaDepartment of Pharmacological and Pharmaceutical Sciences University of Houston Houston TX USA.ORCID https://orcid.org/0000-0003-3509-2446
Bin GuoDepartment of Pharmacological and Pharmaceutical Sciences University of Houston Houston TX USA.ORCID https://orcid.org/0000-0003-3296-9177
University of Houston · USMayo Clinic · USMayo Clinic in Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To discover a novel peptoid antagonist that targets the interleukin-15 (IL-15) receptor and to evaluate its therapeutic efficacy in the treatment of inflammation and arthritis. Methods: A new compound (IFRA3, interleukin-15 receptor antagonist 3) was discovered using a unique on-bead two-colour combinatorial cell screening of a peptoid library. The interaction of IFRA3 with IL-15 receptor was assessed by Results: IFRA3Q1 (a tetrameric derivative of IFRA3) inhibited the activity of IL-15 and suppressed CTLL-2 cell proliferation (which depends on IL-15 activity). IFRA3Q1 exhibited strong Conclusion: By binding to and inhibiting the function of IL-15 receptor, IFRA3Q1 exhibited significant anti-arthritis activity. Our findings suggest that IFRA3Q1 represents a new paradigm for arthritis therapy by targeting IL-15 signalling.

Indexed as

inflammationinterleukin‐15peptoidrheumatoid arthritis

Identifiers

PMID36439637
PMCPMC9686008
OpenAlexW4310464579

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.