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基孔肯雅热驱动的基因表达与破骨细胞存活及慢性关节痛相关。

Chikungunya-Driven Gene Expression Linked to Osteoclast Survival and Chronic Arthralgia.

作者信息

Urbanski Alysson Henrique, Maso Vanessa E, Martins Felipe M, da Costa-Martins André Guilherme, do Nascimento Oliveira Ana Paula B, Nakaya Helder I

机构信息

School of Pharmaceutical Sciences, University of São Paulo, São Paulo 05508-020, Brazil.

Micromanufacturing Laboratory, Institute for Technological Research-IPT, São Paulo 05508-901, Brazil.

出版信息

Infect Dis Rep. 2024 Sep 20;16(5):914-922. doi: 10.3390/idr16050073.

Abstract

Chikungunya fever (CHIKF), caused by the Chikungunya virus (CHIKV), manifests as acute febrile illness often associated with polyarthritis and polyarthralgia. Although the acute symptoms resolve within two weeks, many patients experience prolonged joint pain and inflammation, resembling rheumatoid arthritis (RA). This study aimed to identify molecular markers related to joint pain and chronicity in CHIKV-infected individuals by analyzing blood transcriptomes using bulk RNA sequencing. B- and T-cell receptor (BCR and TCR) diversity was assessed through computational analysis of RNA-seq data, revealing a significant reduction in CDR3 diversity in CHIKV-infected individuals compared to healthy controls. This reduced diversity was associated with the upregulation of genes involved in osteoclast differentiation and activation, particularly through the RANK/RANKL signaling pathway. These findings suggest a potential link between immune dysregulation and enhanced osteoclast activity, which may contribute to the persistence of joint pain in chronic CHIKF. Targeting osteoclast-related pathways could offer therapeutic strategies for managing chronic symptoms in CHIKF patients.

摘要

基孔肯雅热(CHIKF)由基孔肯雅病毒(CHIKV)引起,表现为急性发热性疾病,常伴有多关节炎和多关节痛。尽管急性症状在两周内会消退,但许多患者会经历长时间的关节疼痛和炎症,类似于类风湿性关节炎(RA)。本研究旨在通过使用批量RNA测序分析血液转录组,确定CHIKV感染个体中与关节疼痛和慢性化相关的分子标记。通过对RNA测序数据的计算分析评估B细胞和T细胞受体(BCR和TCR)多样性,结果显示与健康对照相比,CHIKV感染个体的互补决定区3(CDR3)多样性显著降低。这种多样性降低与破骨细胞分化和激活相关基因的上调有关,特别是通过核因子κB受体活化因子/核因子κB受体活化因子配体(RANK/RANKL)信号通路。这些发现提示免疫失调与破骨细胞活性增强之间可能存在联系,这可能导致慢性基孔肯雅热中关节疼痛的持续存在。针对破骨细胞相关通路可能为管理基孔肯雅热患者的慢性症状提供治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd9f/11417755/aaed1fc4e8b5/idr-16-00073-g001.jpg

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