Evidence map›Paper›PMID 37475994›Full record

ArticleJournal of rheumatic diseases2021

Intravenous Administration of Toll-Like Receptor Inhibitory Peptide 1 is Effective for the Treatment of Systemic Lupus Erythematosus in a

Wook-Young Baek, Sung-Min Lee, Sang-Won Lee, In-Ok Son, Sangdun Choi, Chang-Hee Suh

Open access · diamondAbstract read
In one paragraph

Article in Journal of rheumatic diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Gain-of-functionClinical kidney journal · 2022
    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

6 authors at 1 institution in 1 country.

Wook-Young Baek *Department of Rheumatology, Ajou University School of Medicine, Suwon, Korea.
Sung-Min Lee *Department of Rheumatology, Ajou University School of Medicine, Suwon, Korea.
Sang-Won LeeDepartment of Rheumatology, Ajou University School of Medicine, Suwon, Korea.
In-Ok SonDepartment of Rheumatology, Ajou University School of Medicine, Suwon, Korea.
Sangdun ChoiDepartment of Molecular Science and Technology, Ajou University, Suwon, Korea.
Chang-Hee SuhDepartment of Rheumatology, Ajou University School of Medicine, Suwon, Korea.ORCID 0000-0001-6156-393X
Ajou University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Systemic lupus erythematosus (SLE) is a common chronic autoimmune inflammatory disease According to recent studies, signaling through Toll-like receptor (TLR) protein, which promotes the production of inflammatory cytokines, leads to the development of SLE TLR-inhibitory peptide 1 (TIP1) has been newly identified for the treatment of autoimmune diseases. Methods: The effect of TIP1 was analyzed in an SLE mouse model (MRL/ Results: The antinuclear antibody and inflammatory cytokine (interferon-α) in the serum as well as levels of albumin in the urine of the mice in the TIP1 treatment group had decreased when compared to those of mice in the control treatment group Kidney inflammation in mice in the TIP1 treatment group was alleviated The mRNA expression levels of TLR7- or TLR9-related downstream signaling molecules also decreased in all organs of the mice in the TIP1 treatment group. Conclusion: Intravenous treatment with TIP1 reduces symptoms and markers of inflammation in MRL/

Indexed as

InflammationMRL lpr miceSystemic lupus erythematosusToll-like receptor

Identifiers

PMID37475994
PMCPMC10324895
OpenAlexW3175510477

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.