Evidence map›Paper›PMID 37705593›Full record

ArticleACS pharmacology & translational science2023

Prophylactic Mitigation of Acute Graft versus Host Disease by Novel 2-(Pyrrolidin-1-ylmethyl)pyrrole-Based Stimulation-2 (ST2) Inhibitors.

Xinrui Yuan, Hua Jiang, Denggang Fu, Jason C Rech, Aaron Robida, Krishani Rajanayake, Hebao Yuan, Miao He, Bo Wen, Duxin Sun and 5 more

Open access · greenAbstract read
In one paragraph

Article in ACS pharmacology & translational science, 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
0.5field-weighted citation impact, top 31% 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, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. 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

15 authors at 4 institutions in 1 country.

Xinrui YuanDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, Memphis, Tennessee 38163, United States.
Hua JiangDepartment of Microbiology & Immunology, Medical University of South Carolina, Charleston, South Carolina 29425-2503, United States.
Denggang FuDepartment of Microbiology & Immunology, Medical University of South Carolina, Charleston, South Carolina 29425-2503, United States.
Jason C RechMichigan Center for Therapeutic Innovation, Department of Internal Medicine, Life Sciences Institute, Department of Pharmaceutical Sciences, College of Pharmacy, and Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Aaron RobidaMichigan Center for Therapeutic Innovation, Department of Internal Medicine, Life Sciences Institute, Department of Pharmaceutical Sciences, College of Pharmacy, and Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Krishani RajanayakeMichigan Center for Therapeutic Innovation, Department of Internal Medicine, Life Sciences Institute, Department of Pharmaceutical Sciences, College of Pharmacy, and Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Hebao YuanMichigan Center for Therapeutic Innovation, Department of Internal Medicine, Life Sciences Institute, Department of Pharmaceutical Sciences, College of Pharmacy, and Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.ORCID https://orcid.org/0000-0003-4425-3678
Miao HeMichigan Center for Therapeutic Innovation, Department of Internal Medicine, Life Sciences Institute, Department of Pharmaceutical Sciences, College of Pharmacy, and Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Bo WenMichigan Center for Therapeutic Innovation, Department of Internal Medicine, Life Sciences Institute, Department of Pharmaceutical Sciences, College of Pharmacy, and Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Duxin SunMichigan Center for Therapeutic Innovation, Department of Internal Medicine, Life Sciences Institute, Department of Pharmaceutical Sciences, College of Pharmacy, and Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.ORCID https://orcid.org/0000-0002-6406-2126
Chen LiuDepartment of Pathology, Yale University, New Haven, Connecticut 06520, United States.
Krishnapriya ChinnaswamyMichigan Center for Therapeutic Innovation, Department of Internal Medicine, Life Sciences Institute, Department of Pharmaceutical Sciences, College of Pharmacy, and Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Jeanne A StuckeyMichigan Center for Therapeutic Innovation, Department of Internal Medicine, Life Sciences Institute, Department of Pharmaceutical Sciences, College of Pharmacy, and Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan 48109, United States.
Sophie PaczesnyDepartment of Microbiology & Immunology, Medical University of South Carolina, Charleston, South Carolina 29425-2503, United States.
Chao-Yie YangDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, Memphis, Tennessee 38163, United States.ORCID https://orcid.org/0000-0002-5445-0109
University of Michigan · USMedical University of South Carolina · USUniversity of Tennessee Health Science Center · USYale University · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Eric R. Fearon · 1988 to 2026
$178.2M
Translating Novel Drug-Targetable Biomarkers to Treat Graft versus Host DiseaseR01CA168814 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI PACZESNY, SOPHIE · 2013 to 2024
$3.0M
Development of first-in-class ST2 inhibitors for treating graft-versus-host diseaseR01HL141432 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI PACZESNY, SOPHIE, YANG, CHAO-YIE · 2019 to 2022
$2.6M
NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA168814NHLBI NIH HHS R01 HL141432
6 · The paper itself

Abstract

Hematopoietic cell transplantation (HCT) is a proven and potentially curable therapy for hematological malignancies and inherited hematological disease. The main risk of HCT is the development of graft versus host disease (GVHD) acquired in up to 50% of patients. Upregulation of soluble ST2 (sST2) is a key clinical biomarker for GVHD prognosis and was shown to be a potential therapeutic target for GVHD. Agents targeting sST2 to reduce the sST2 level after HCT have the potential to mitigate GVHD progression. Here, we report

Identifiers

PMID37705593
PMCPMC10496145
OpenAlexW4385878501

What OpenQuestion holds

Textmetadata
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.