Evidence map›Paper›PMID 37215126›Full record

ArticleFrontiers in immunology2023

Cell-penetrating TLR inhibitor peptide alleviates ulcerative colitis by the functional modulation of macrophages.

Bikash Thapa, Seongwon Pak, Dohyeon Chung, Hye Kyoung Shin, Seong Ho Lee, Keunwook Lee

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
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  4. Frontiers in immunology · 2026
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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

6 authors at 1 institution in 1 country.

Bikash ThapaInstitute of Bioscience & Biotechnology, Hallym University, Chuncheon, Republic of Korea.
Seongwon PakDepartment of Biomedical Science, Hallym University, Chuncheon, Republic of Korea.
Dohyeon ChungDepartment of Biomedical Science, Hallym University, Chuncheon, Republic of Korea.
Hye Kyoung ShinR&D Center, Genesen Co., Ltd, Seoul, Republic of Korea.
Seong Ho LeeR&D Center, Genesen Co., Ltd, Seoul, Republic of Korea.
Keunwook LeeInstitute of Bioscience & Biotechnology, Hallym University, Chuncheon, Republic of Korea.
Hallym University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toll-like receptors (TLRs) have a crucial role not only in triggering innate responses against microbes but in orchestrating an appropriate adaptive immunity. However, deregulated activation of TLR signaling leads to chronic inflammatory conditions such as inflammatory bowel disease (IBD). In this study, we evaluated the immunomodulatory potential of a TLR inhibitor in the form of a cell-penetrating peptide using an ulcerative colitis animal model. A peptide derived from the TIR domain of the TLR adaptor molecule TIRAP that was conjugated with a cell-penetrating sequence (cpTLR-i) suppressed the induction of pro-inflammatory cytokines such as TNF-α and IL-1β in macrophages. In DSS-induced colitis mice, cpTLR-i treatment ameliorated colitis symptoms, colonic tissue damage, and mucosal inflammation. Intriguingly, cpTLR-i attenuated the induction of TNF-α-expressing proinflammatory macrophages while promoting that of regulatory macrophages expressing arginase-1 and reduced type 17 helper T cell (Th17) responses in the inflamed colonic lamina propria. An

Indexed as

Cell-Penetrating PeptidesColitisColitis, UlcerativeInflammatory Bowel DiseasesAnimalsMacrophagesMiceTumor Necrosis Factor-alphaCell-Penetrating PeptidesTumor Necrosis Factor-alphacell-penetrating TLR inhibitor peptidemacrophagetoll-like receptorstype 17 helper T cellsulcerative colitis

Identifiers

PMID37215126
PMCPMC10196052
OpenAlexW4377565541

What OpenQuestion holds

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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.