Evidence map›Paper›PMID 40635492›Full record

ArticleThe Korean journal of internal medicine2025

Decreased frequency and inflammatory change of FoxP3+ regulatory T cells in immunopathogenesis of human acute graft-versus-host disease.

Nayeon Seong, Cheongin Yang, Kunye Kwak, Ka-Won Kang, Yong Park, Byung Soo Kim, Seong Hyun Jeong, Joon Seong Park, Yoon Seok Choi

Abstract read
In one paragraph

Article in The Korean journal of internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. 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

9 authors.

Nayeon SeongDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Cheongin YangDepartment of Hematology-Oncology, Ajou University School of Medicine, Suwon, Korea.
Kunye KwakDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Ka-Won KangDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Yong ParkDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Byung Soo KimDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Seong Hyun JeongDepartment of Hematology-Oncology, Ajou University School of Medicine, Suwon, Korea.
Joon Seong ParkDepartment of Hematology-Oncology, Ajou University School of Medicine, Suwon, Korea.
Yoon Seok ChoiDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.

Funding

Ministry of Science and ICTNational Research Foundation of Korea 2018R1C1B6008261National Research Foundation of Korea RS-2022-NR070625
6 · The paper itself

Abstract

BACKGROUND/

aimsAcute graft-versus-host disease (GvHD) is a severe complication of allogeneic stem cell transplantation, characterized by immune-mediated tissue damage primarily affecting the skin, liver, and gastrointestinal tract. Regulatory T (Treg) cells play a critical role in maintaining immune homeostasis. However, the pathogenic roles of changes in Treg cell number and function on acute GvHD remain poorly understood. This study aimed to investigate the quantitative and qualitative changes in Treg cells and their clinical and pathogenic implication of acute GvHD.

methodsA total of 62 patients who underwent allogeneic stem cell transplantation at a tertiary institution from 2019 to 2024 were enrolled. Peripheral blood mononuclear cells were isolated and analyzed by multicolor flow cytometry. Treg cell subsets and cytokine production were assessed after T-cell receptor stimulation. Serum levels of inflammatory cytokines were measured using cytometric bead array, and Treg cell suppressive function was evaluated through co-culture experiments.

resultsPatients with acute GvHD showed a decreased frequency of circulating Treg cells, with a notable increase in the CD45RA-FoxP3lo pro-inflammatory subset. Treg cells produced inflammatory cytokines including TNF-α upon stimulation and exhibited reduced suppressive activity. The frequency of TNF-α+ Treg cells correlated with the clinical severity of acute GvHD. Elevated serum levels of IL-6 and IL-21 were associated with the inflammatory conversion of Treg cells.

conclusionDuring human acute GvHD, frequencies of circulating Treg cells are significantly decreased. Inflammatory change of Treg cells, represented by TNF-α production and reduced suppressive capacity, contributes to the immunopathogenesis of acute GvHD.

Indexed as

Forkhead Transcription FactorsGraft vs Host DiseaseHematopoietic Stem Cell TransplantationT-Lymphocytes, RegulatoryAcute DiseaseAdultCytokinesFemaleHumansInflammation MediatorsMaleMiddle AgedYoung AdultCytokinesForkhead Transcription FactorsFOXP3 protein, humanInflammation MediatorsGraft-versus-host diseaseHematopoietic stem cell transplantationInflammationRegulatory T cellTNF-alpha

Identifiers

PMID40635492
PMCPMC12257019

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