Single-cell transcriptome reveals potential mechanisms for gout in children

ObjectivePediatric gout is a condition that differs from traditional adult gout and has attracted significant attention. This study aims to explore the molecular mechanisms underlying pediatric gout.MethodsWe analyzed peripheral blood samples from pediatric gout patients and healthy controls using s...

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Main Authors: Shengyou Yu, Ren Qi, Liang Xiao, YiHui Huang, Li Yu
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-04-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2025.1577109/full
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author Shengyou Yu
Ren Qi
Liang Xiao
YiHui Huang
Li Yu
author_facet Shengyou Yu
Ren Qi
Liang Xiao
YiHui Huang
Li Yu
author_sort Shengyou Yu
collection DOAJ
description ObjectivePediatric gout is a condition that differs from traditional adult gout and has attracted significant attention. This study aims to explore the molecular mechanisms underlying pediatric gout.MethodsWe analyzed peripheral blood samples from pediatric gout patients and healthy controls using single-cell RNA sequencing (scRNA-seq). Statistical tests were employed to analyze the data and identify significant differences between the groups.ResultsOur findings revealed that CD14+ monocytes and DN T cells play crucial roles in pediatric gout. CD14+ monocytes are essential for recognizing and phagocytosing monosodium urate (MSU) crystals, triggering inflammation. DN T cells may be involved in the adaptive immune response within gouty joints. These cells not only contribute to the inflammatory response but also interact with other immune cells, amplifying the inflammatory cascade. Comparative analysis with adult gout studies highlighted both similarities and differences in cellular and molecular mechanisms between children and adults. The CD14+ monocytes may be interact with other immune cells through the TNF-α/NF-κB signaling pathway. Targeting this pathway may offer therapeutic potential for managing pediatric gout.ConclusionThe results provide a foundation for new diagnostic markers and therapeutic targets for pediatric gout. They also pave the way for future research and the development of targeted therapies that can effectively manage and potentially prevent the debilitating effects of gout in children. Understanding the unique molecular mechanisms in pediatric gout could influence treatment strategies and improve patient outcomes.
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issn 1664-3224
language English
publishDate 2025-04-01
publisher Frontiers Media S.A.
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series Frontiers in Immunology
spelling doaj-art-16508012bf484b8797db1d2285fb839e2025-08-20T02:56:01ZengFrontiers Media S.A.Frontiers in Immunology1664-32242025-04-011610.3389/fimmu.2025.15771091577109Single-cell transcriptome reveals potential mechanisms for gout in childrenShengyou Yu0Ren Qi1Liang Xiao2YiHui Huang3Li Yu4Department of Pediatrics, Guangzhou First People’s Hospital, South China University of Technology, Guangzhou, Guangdong, ChinaDepartment of Rheumatology and Immunology, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, ChinaDepartment of Pediatrics, Guangzhou First People’s Hospital, South China University of Technology, Guangzhou, Guangdong, ChinaDepartment of Pediatrics, Guangzhou Red Cross Hospital of Jinan University, Guangzhou, Guangdong, ChinaDepartment of Pediatrics, Guangzhou First People’s Hospital, South China University of Technology, Guangzhou, Guangdong, ChinaObjectivePediatric gout is a condition that differs from traditional adult gout and has attracted significant attention. This study aims to explore the molecular mechanisms underlying pediatric gout.MethodsWe analyzed peripheral blood samples from pediatric gout patients and healthy controls using single-cell RNA sequencing (scRNA-seq). Statistical tests were employed to analyze the data and identify significant differences between the groups.ResultsOur findings revealed that CD14+ monocytes and DN T cells play crucial roles in pediatric gout. CD14+ monocytes are essential for recognizing and phagocytosing monosodium urate (MSU) crystals, triggering inflammation. DN T cells may be involved in the adaptive immune response within gouty joints. These cells not only contribute to the inflammatory response but also interact with other immune cells, amplifying the inflammatory cascade. Comparative analysis with adult gout studies highlighted both similarities and differences in cellular and molecular mechanisms between children and adults. The CD14+ monocytes may be interact with other immune cells through the TNF-α/NF-κB signaling pathway. Targeting this pathway may offer therapeutic potential for managing pediatric gout.ConclusionThe results provide a foundation for new diagnostic markers and therapeutic targets for pediatric gout. They also pave the way for future research and the development of targeted therapies that can effectively manage and potentially prevent the debilitating effects of gout in children. Understanding the unique molecular mechanisms in pediatric gout could influence treatment strategies and improve patient outcomes.https://www.frontiersin.org/articles/10.3389/fimmu.2025.1577109/fullpediatric goutsingle-cell RNA sequencingCD14+ monocytesDN T cellsinflammatory mechanisms children
spellingShingle Shengyou Yu
Ren Qi
Liang Xiao
YiHui Huang
Li Yu
Single-cell transcriptome reveals potential mechanisms for gout in children
Frontiers in Immunology
pediatric gout
single-cell RNA sequencing
CD14+ monocytes
DN T cells
inflammatory mechanisms children
title Single-cell transcriptome reveals potential mechanisms for gout in children
title_full Single-cell transcriptome reveals potential mechanisms for gout in children
title_fullStr Single-cell transcriptome reveals potential mechanisms for gout in children
title_full_unstemmed Single-cell transcriptome reveals potential mechanisms for gout in children
title_short Single-cell transcriptome reveals potential mechanisms for gout in children
title_sort single cell transcriptome reveals potential mechanisms for gout in children
topic pediatric gout
single-cell RNA sequencing
CD14+ monocytes
DN T cells
inflammatory mechanisms children
url https://www.frontiersin.org/articles/10.3389/fimmu.2025.1577109/full
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AT renqi singlecelltranscriptomerevealspotentialmechanismsforgoutinchildren
AT liangxiao singlecelltranscriptomerevealspotentialmechanismsforgoutinchildren
AT yihuihuang singlecelltranscriptomerevealspotentialmechanismsforgoutinchildren
AT liyu singlecelltranscriptomerevealspotentialmechanismsforgoutinchildren