Evidence map›Paper›PMID 40121226›Full record

ArticleScientific reports2025

Innovative peptide therapeutics targeting IL17RA to regulate inflammatory responses.

Xinmin Wang, Hang Bao, Yuya Wang, Yalu Wang, Cheng Guo, Yanning Wu, Yongbin Xu, Yali Li

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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
–field-weighted citation impact
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.

  1. Article
  2. FromFrontiers in immunology · 2026
    Article
  3. Review
  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

8 authors.

Xinmin WangSchool of Life Science and Technology, Inner Mongolia University of Science and Technology, Baotou, 014010, China.
Hang BaoSchool of Life Science and Technology, Inner Mongolia University of Science and Technology, Baotou, 014010, China.
Yuya WangInner Mongolia Autonomous Region People's Hospital, Hohhot, 010010, China.
Yalu WangThe First Affiliated Hospital of Baotou Medical College, Inner Mongolia University of Science and Technology, Baotou, 014010, China.
Cheng GuoSchool of Life Science and Technology, Inner Mongolia University of Science and Technology, Baotou, 014010, China.
Yanning WuSchool of Life Science and Technology, Inner Mongolia University of Science and Technology, Baotou, 014010, China.
Yongbin XuSchool of Life Science and Technology, Inner Mongolia University of Science and Technology, Baotou, 014010, China.
Yali LiSchool of Life Science and Technology, Inner Mongolia University of Science and Technology, Baotou, 014010, China. btliyali@126.com.

Funding

Fundamental Research Funds for Inner Mongolia University of Science & Technology 2023QNJS149National Natural Science Foundation of China 82460323Natural Science Foundation of Inner Mongolia Autonomous Region 2023QN08018
6 · The paper itself

Abstract

Interleukin-17 receptor A (IL17RA) is a critical mediator of pro-inflammatory cytokine signaling and a key immune checkpoint in autoimmune diseases. While monoclonal antibodies targeting IL17RA have demonstrated clinical efficacy, their high costs, complexity in production, and lack of oral bioavailability present significant limitations. In response to these challenges, we developed AL-8(0), a novel peptide specifically designed to inhibit the IL17A-IL17RA signaling pathway. AL-8(0) was synthesized with high purity and systematically evaluated for its binding affinity and anti-inflammatory activity. Biophysical and cellular assays confirmed the peptide's strong affinity for IL17RA and its ability to inhibit inflammatory cytokine production in IL17RA-expressing monocyte-macrophages and keratinocytes. Moreover, its anti-inflammatory effects were com-parable to IL17RA-targeting monoclonal antibodies and were dependent on IL17RA expression, as demonstrated by experiments using IL17RA-deficient cells. These results underscore AL-8(0)'s potential as a targeted therapeutic for autoimmune diseases, offering a peptide-based alternative with lower antigenicity, improved scalability, and potential for oral administration. This study lays the groundwork for further development of AL-8(0) and similar peptides as innovative treatments for inflammatory disorders driven by the IL17A-IL17RA pathway.

Indexed as

Anti-Inflammatory AgentsInflammationPeptidesReceptors, Interleukin-17AnimalsHumansInterleukin-17KeratinocytesMacrophagesMiceSignal TransductionAnti-Inflammatory AgentsIL17RA protein, humanInterleukin-17PeptidesReceptors, Interleukin-17AutoimmunityInflammationInterleukin-17 receptorPeptideTargeted therapy

Identifiers

PMID40121226
PMCPMC11929782

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Registered trials

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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.