Evidence map›Paper›PMID 33347507›Full record

ArticlePloS one2020

Association of soluble T cell immunoglobulin domain and mucin-3 (sTIM-3) and mac-2 binding protein glycosylation isomer (M2BPGi) in patients with autoimmune hepatitis.

Kiyoshi Migita, Minoru Nakamura, Yoshihiro Aiba, Hideko Kozuru, Seigo Abiru, Atsumasa Komori, Yuya Fujita, Junpei Temmoku, Tomoyuki Asano, Shuzo Sato and 11 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Elevated Serum Soluble Tim-3 in Primary Biliary Cholangitis: Lack of Correlation with Cytokines, Chemokines, and Clinical Parameters.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. 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

21 authors at 6 institutions in 1 country.

Kiyoshi MigitaClinical Research Center, Nagasaki Medical Center, Nagasaki, Japan.ORCID 0000-0003-1339-5622
Minoru NakamuraClinical Research Center, Nagasaki Medical Center, Nagasaki, Japan.
Yoshihiro AibaClinical Research Center, Nagasaki Medical Center, Nagasaki, Japan.
Hideko KozuruClinical Research Center, Nagasaki Medical Center, Nagasaki, Japan.
Seigo AbiruClinical Research Center, Nagasaki Medical Center, Nagasaki, Japan.
Atsumasa KomoriClinical Research Center, Nagasaki Medical Center, Nagasaki, Japan.
Yuya FujitaDepartment of Rheumatology, Fukushima Medical University, Fukushima, Japan.
Junpei TemmokuDepartment of Rheumatology, Fukushima Medical University, Fukushima, Japan.
Tomoyuki AsanoDepartment of Rheumatology, Fukushima Medical University, Fukushima, Japan.
Shuzo SatoDepartment of Rheumatology, Fukushima Medical University, Fukushima, Japan.
Makiko FuruyaDepartment of Rheumatology, Fukushima Medical University, Fukushima, Japan.
Atsushi NaganumaNational Hospital Organization, Takasaki Medical Center, Takasaki, Japan.
Kaname YoshizawaNational Hospital Organization, Shinsyu-Ueda Medical Center, Ueda, Nagano, Japan.
Masaaki ShimadaNational Hospital Organization, Nagoya Medical Center, Nagoya, Aichi, Japan.
Keisuke ArioNational Hospital Organization, Ureshino Medical Center, Ureshino, Saga, Japan.
Tomohiko MannamiNational Hospital Organization, Okayama Medical Center, Okayama, Okayama, Japan.
Hiroshi KohnoNational Hospital Organization, Kure Medical Center, Kure, Hiroshima, Japan.
Toshihiko KaneyoshiNational Hospital Organization, Fukuyama Medical Center, Kanazawa, Ishikawa, Japan.
Takuya KomuraNational Hospital Organization, Kanazawa Medical Center, Kanazawa, Ishikawa, Japan.
Hiromasa OhiraDepartment of Gastroenterology, Fukushima Medical University, Fukushima, Japan.
Hiroshi YatsuhashiClinical Research Center, Nagasaki Medical Center, Nagasaki, Japan.
Fukushima Medical University · JPNagasaki Medical Center · JPNational Hospital Organization · JPFukuyama Cardiovascular Hospital · JPKanazawa Medical Center · JPNational Hospital Organization Takasaki Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutoimmune hepatitis (AIH) is a disorder of unknown etiology in which immune-mediated liver injury progress to cirrhosis or hepatocellular carcinoma (HCC). The aim of the present study was to determine whether circulating soluble TIM3 (sTIM3) is elevated in patients with AIH patients and whether sTIM-3 levels are associated with clinical parameters of AIH.

methodsWe enrolled 123 Japanese patients with AIH who were identified from the National Hospital Organization-AIH-liver-network database, as well as 32 patients with chronic hepatitis C (CHC), 30 patients with primary biliary cholangitis (PBC) and healthy control subjects. Serum sTIM-3 concentrations were quantified by ELISA.

resultsSerum levels of sTIM-3 were significantly higher in AIH patients (median 4865 pg/ml; [interquartile range (IQR); 3122-7471]) compared to those in CHC (1026 pg/ml [IQR: 806-1283] p<0.001), PBC (2395 pg/ml [IQR: 2012-3422] p<0.001) or healthy controls (1285 pg/ml [IQR: 1098-1812] p<0.001). In AIH group, serum sTIM-3 were correlated with alanine aminotransferase (ALT), or total bilirubin (TB) and negatively correlated with serum levels of albumin (Alb). Serum levels of sTIM-3 were also strongly correlated with Mac-2 binding protein glycosylation isomer (M2BPGi) levels, but did not correlate with the histological grade of liver fibrosis. Steroid treatment of AIH patients significantly reduced serum sTIM-3 levels (2147±623pg/ml versus 1321±378pg/ml, p<0.001).

conclusionsCirculating sTIM-3 levels were elevated in AIH patients and are associated with AIH disease activity and AIH-related liver damage. These findings indicate that serum sTIM-3 correlated with disease status of AIH and could be useful biomarkers to detect autoimmune-mediated liver injury. Our data suggest a possible link between the TIM-3/GAL-9 pathway and AIH severity or phenotype, and further investigations of the TIM-3 pathway and AIH pathophysiology is warranted.

Indexed as

AgedAlanine TransaminaseAlbuminsBilirubinFemaleGalectin 3GlycosylationHepatitis, AutoimmuneHepatitis C, ChronicHumansImmunoglobulin DomainsLiverMaleMiddle AgedMucin-3T-LymphocytesAlanine TransaminaseAlbuminsBilirubinGalectin 3Mucin-3

Identifiers

PMID33347507
PMCPMC7751864
OpenAlexW3115971468

What OpenQuestion 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 OpenQuestion graph.