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用于预测基孔肯雅病毒感染后慢性风湿性疾病的急性免疫学生物标志物

Acute Immunological Biomarkers for Predicting Chronic Rheumatologic Disease After Chikungunya Virus Infection.

作者信息

Lozano-Parra Anyela, Herrera Víctor, Villar Luis Ángel, Urcuqui-Inchima Silvio, Valdés-López Juan Felipe, Garrido Elsa Marina Rojas

机构信息

Grupo Epidemiología Clínica, Escuela de Medicina, Universidad Industrial de Santander UIS, Calle 9 Carrera 27, Bucaramanga 680002, Colombia.

Centro de Atención y Diagnóstico de Enfermedades Infecciosas (CDI), Fundación INFOVIDA, Cra. 37 No. 51-126, Bucaramanga 680003, Colombia.

出版信息

Trop Med Infect Dis. 2025 Jul 11;10(7):195. doi: 10.3390/tropicalmed10070195.

Abstract

Early biomarkers are needed to predict the long-term persistence of rheumatical symptoms in patients infected with Chikungunya virus (CHIKV). This nested case-control study aimed to assess immunological factors during the early phases of CHIKV infection to predict the risk of post-CHIK chronic rheumatism (pCHIK-CR) in adult patients of two prospective cohorts. We evaluated 46 febrile patients (median age: 33.5 years; IQR: 19 years; women: 50.0%) with CHIKV infection confirmed during the 2014-2015 outbreak in Santander, Colombia. The participants were classified by a rheumatologist as either cases (pCHIK-CR) or controls (WoRM, without rheumatical manifestations). We quantified serum levels of IL-4, IL-6, IL-8/CXCL-8, IL-27, CCL-2, CXCL-9, CXCL-10, and IgG using Luminex and ELISA assays during the acute and subacute phases of infection. Then, we evaluated the association of these immune factors with the case-control status using piecewise logistic regression adjusted for age and sex. There were non-linear associations between IL-8/CXCL-8, CXCL-9, and CXCL-10 with pCHIK-CR. Increases in the levels of IL-8/CXCL-8 (<35.7 pg/mL), CXCL-9 (≥6000 pg/mL), and CXCL-10 (≥36,800 pg/mL) were significantly associated with a reduced risk of pCHIK-CR (adjusted ORs: 0.85, 0.96, and 0.94, respectively). These results suggest that increases in IL-8/CXCL-8, CXCL-9, and CXCL-10 levels, measured in the early stages of CHIKV infection, may predict a chronic disease risk. This suggests the possibility that an early and strong immune response could contribute to enhancing CHIKV control and potentially reduce the risk of persistent joint symptoms. Given their expression patterns and timing, these three immune factors may be considered promising biomarker candidates for assessing the risk of chronic rheumatologic disease. These findings should be considered as exploratory and validated in additional cohort studies.

摘要

需要早期生物标志物来预测感染基孔肯雅病毒(CHIKV)患者风湿症状的长期持续性。这项巢式病例对照研究旨在评估CHIKV感染早期阶段的免疫因素,以预测两个前瞻性队列成年患者中CHIKV感染后慢性风湿病(pCHIK-CR)的风险。我们评估了46例发热患者(中位年龄:33.5岁;四分位间距:19岁;女性:50.0%),这些患者在2014 - 2015年哥伦比亚桑坦德疫情期间确诊感染CHIKV。参与者由一名风湿病学家分类为病例(pCHIK-CR)或对照(WoRM,无风湿表现)。我们在感染的急性期和亚急性期使用Luminex和ELISA检测法对血清中白细胞介素-4(IL-4)、白细胞介素-6(IL-6)、白细胞介素-8/CXC趋化因子配体8(IL-8/CXCL-8)、白细胞介素-27(IL-27)、CC趋化因子配体2(CCL-2)、CXC趋化因子配体9(CXCL-9)、CXC趋化因子配体10(CXCL-10)和免疫球蛋白G(IgG)水平进行了定量。然后,我们使用针对年龄和性别进行调整的分段逻辑回归评估了这些免疫因素与病例对照状态之间的关联。IL-8/CXCL-8、CXCL-9和CXCL-10与pCHIK-CR之间存在非线性关联。IL-8/CXCL-8(<35.7 pg/mL)、CXCL-9(≥6000 pg/mL)和CXCL-10(≥36,800 pg/mL)水平升高与pCHIK-CR风险降低显著相关(调整后的比值比分别为:0.85、0.96和0.94)。这些结果表明,在CHIKV感染早期阶段检测到的IL-8/CXCL-8、CXCL-9和CXCL-10水平升高可能预测慢性疾病风险。这表明早期强烈的免疫反应可能有助于加强对CHIKV的控制并潜在降低持续性关节症状的风险。鉴于它们的表达模式和时间,这三种免疫因素可能被认为是评估慢性风湿性疾病风险的有前景的生物标志物候选物。这些发现应被视为探索性的,并在其他队列研究中进行验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a631/12300443/5d821d605419/tropicalmed-10-00195-g001.jpg

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