Evidence map›Paper›PMID 37957274›Full record

ArticleScientific reports2023

An immunomodulating peptide with potential to suppress tumour growth and autoimmunity.

Michael Agrez, Christopher Chandler, Kristofer J Thurecht, Nicholas L Fletcher, Feifei Liu, Gayathri Subramaniam, Christopher B Howard, Benjamin Blyth, Stephen Parker, Darryl Turner and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. An Immunomodulating Peptide With Potential to Counteract Endometriosis.The Australian & New Zealand journal of obstetrics & gynaecology · 2026
    Article
  3. Article
  4. Review
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

16 authors at 4 institutions in 2 countries.

Michael AgrezInterK Peptide Therapeutics Limited, New South Wales, Australia. michael.agrez@interk.com.au.
Christopher ChandlerAuspep Pty Limited, Melbourne, Australia.
Kristofer J ThurechtCentre for Advanced Imaging, University of Queensland, Brisbane, Australia.
Nicholas L FletcherCentre for Advanced Imaging, University of Queensland, Brisbane, Australia.
Feifei LiuCentre for Advanced Imaging, University of Queensland, Brisbane, Australia.
Gayathri SubramaniamCentre for Advanced Imaging, University of Queensland, Brisbane, Australia.
Christopher B HowardCentre for Advanced Imaging, University of Queensland, Brisbane, Australia.
Benjamin BlythDepartment of Oncology,, Peter MacCallum Cancer Centre and Sir Peter MacCallum, University of Melbourne, Melbourne, Australia.
Stephen ParkerInterK Peptide Therapeutics Limited, New South Wales, Australia.
Darryl TurnerConcept Life Sciences, Edinburgh, Scotland.
Justyna RzepeckaConcept Life Sciences, Edinburgh, Scotland.
Gavin KnoxConcept Life Sciences, Edinburgh, Scotland.
Anastasia NikaConcept Life Sciences, Edinburgh, Scotland.
Andrew M HallConcept Life Sciences, Edinburgh, Scotland.
Hayley GoodingConcept Life Sciences, Edinburgh, Scotland.
Laura GallagherConcept Life Sciences, Edinburgh, Scotland.
Concept Life Sciences (United Kingdom) · GBUniversity of Queensland · AUNational Imaging Facility · AUUniversity of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancers and autoimmune diseases commonly co-exist and immune checkpoint inhibitor therapy (ICI) exacerbates autoimmune pathologies. We recently described a lipidic peptide, designated IK14004, that promotes expansion of immunosuppressive T regulatory (Treg) cells and uncouples interleukin-2 from interferon-gamma production while activating CD8+ T cells. Herein, we report IK14004-mediated inhibition of Lewis lung cancer (LLC) growth and re-invigoration of splenocyte-derived exhausted CD4+ T cells. In human immune cells from healthy donors, IK14004 modulates expression of the T cell receptor α/β subunits, induces Type I IFN expression, stimulates natural killer (NK) cells to express NKG2D/NKp44 receptors and enhances K562 cytotoxicity. In both T and NK cells, IK14004 alters the IL-12 receptor β1/β2 chain ratio to favour IL-12p70 binding. Taken together, this novel peptide offers an opportunity to gain further insight into the complexity of ICI immunotherapy so that autoimmune responses may be minimised without promoting tumour evasion from the immune system.

Indexed as

Autoimmune DiseasesCarcinoma, Lewis LungAnimalsAutoimmunityHumansKiller Cells, NaturalT-Lymphocytes, Regulatory

Identifiers

PMID37957274
PMCPMC10643673
OpenAlexW4388638867

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.