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新诊断免疫性血小板减少症患儿循环CXCR5⁺ T细胞的表达模式及作用

The expression pattern and role of circulating CXCR5 T cells in children with newly diagnosed immune thrombocytopenia.

作者信息

Wang Jian-Yong, Xin Yi, Wang Xiao-Li, Li Lin-Lin, Li Ai-Min, Zhang Xiao-Lu

机构信息

Department of Pediatrics, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.

Department of Clinical Laboratory, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.

出版信息

Front Pediatr. 2025 Aug 11;13:1646877. doi: 10.3389/fped.2025.1646877. eCollection 2025.

Abstract

INTRODUCTION

Immune thrombocytopenia (ITP) is the most common bleeding disorder in children. Tfh cells play a crucial role in the pathogenesis of ITP by promoting the production of anti-platelet autoantibodies. Recent studies have shown that CXCR5 T cells not only possess "Tfh-like" cell functions but also can induce Tfh cell differentiation. However, it remains unknown whether CXCR5 T cells are involved in the pathogenesis of ITP. This study aims to investigate the role of CXCR5 T cells in children with newly diagnosed ITP (nITP).

METHODS

A total of 96 children with nITP and 48 healthy children were enrolled in this study. FCM was used to compare the frequencies of circulating CXCR5 T cells and circulating Tfh cells, as well as the levels of ICOS and CD40l on circulating CXCR5 T cells in both groups. The correlation between circulating CXCR5 T cells and platelets as well as circulating Tfh cells were further analyzed.

RESULTS

Compared with healthy controls, the frequency of circulating CXCR5 T cells was higher in children with nITP, and it was negatively correlated with platelet count. The levels of ICOS and CD40l on circulating CXCR5 T cells in children with nITP were also higher. Children with nITP had a higher frequency of circulating Tfh cells, which was positively correlated with circulating CXCR5 T cells.

CONCLUSIONS

The excessive activation and proliferation of CXCR5 T cells may contribute to the pathogenesis of nITP in children. Therefore, it can be used as a target for the immunotherapy of pediatric ITP.

摘要

引言

免疫性血小板减少症(ITP)是儿童最常见的出血性疾病。滤泡辅助性T细胞(Tfh细胞)通过促进抗血小板自身抗体的产生在ITP发病机制中起关键作用。最近的研究表明,CXCR5⁺ T细胞不仅具有“类Tfh”细胞功能,还能诱导Tfh细胞分化。然而,CXCR5⁺ T细胞是否参与ITP发病机制尚不清楚。本研究旨在探讨CXCR5⁺ T细胞在新诊断ITP(nITP)患儿中的作用。

方法

本研究共纳入96例nITP患儿和48例健康儿童。采用流式细胞术(FCM)比较两组循环CXCR5⁺ T细胞和循环Tfh细胞的频率,以及循环CXCR5⁺ T细胞上ICOS和CD40l的水平。进一步分析循环CXCR5⁺ T细胞与血小板以及循环Tfh细胞之间的相关性。

结果

与健康对照组相比,nITP患儿循环CXCR5⁺ T细胞频率更高,且与血小板计数呈负相关。nITP患儿循环CXCR5⁺ T细胞上ICOS和CD40l的水平也更高。nITP患儿循环Tfh细胞频率更高,且与循环CXCR5⁺ T细胞呈正相关。

结论

CXCR5⁺ T细胞的过度活化和增殖可能参与了儿童nITP的发病机制。因此,它可作为儿童ITP免疫治疗的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853e/12375633/14cd53f1dba8/fped-13-1646877-g001.jpg

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