基孔肯雅病毒驱动的基因表达与破骨细胞存活和慢性关节痛有关

IF 3.4 Q2 INFECTIOUS DISEASES Infectious Disease Reports Pub Date : 2024-09-20 DOI:10.3390/idr16050073
Alysson Henrique Urbanski, Vanessa E Maso, Felipe M Martins, André Guilherme da Costa-Martins, Ana Paula B do Nascimento Oliveira, Helder I Nakaya
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引用次数: 0

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,通常伴有多关节炎和多关节痛。虽然急性症状会在两周内缓解,但许多患者会经历长期的关节疼痛和炎症,类似于类风湿性关节炎(RA)。本研究旨在通过使用大量 RNA 测序分析血液转录组,确定与 CHIKV 感染者关节疼痛和慢性病相关的分子标记。通过对RNA-seq数据进行计算分析,评估了B细胞和T细胞受体(BCR和TCR)的多样性,结果显示,与健康对照组相比,CHIKV感染者的CDR3多样性显著降低。这种多样性的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 RANK/RANKL 信号通路。这些研究结果表明,免疫失调与破骨细胞活性增强之间存在潜在联系,这可能是导致慢性CHIKF患者关节疼痛持续存在的原因。针对破骨细胞相关通路可为控制CHIKF患者的慢性症状提供治疗策略。
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Chikungunya-Driven Gene Expression Linked to Osteoclast Survival and Chronic Arthralgia.

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.

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来源期刊
Infectious Disease Reports
Infectious Disease Reports INFECTIOUS DISEASES-
CiteScore
5.10
自引率
0.00%
发文量
82
审稿时长
11 weeks
期刊最新文献
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