基孔肯雅病毒感染后预测慢性风湿病的急性免疫生物标志物。

IF 2.6 4区 医学 Q2 INFECTIOUS DISEASES
Anyela Lozano-Parra, Víctor Herrera, Luis Ángel Villar, Silvio Urcuqui-Inchima, Juan Felipe Valdés-López, Elsa Marina Rojas Garrido
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引用次数: 0

摘要

需要早期生物标志物来预测感染基孔肯雅病毒(CHIKV)的患者风湿病症状的长期持续性。本巢式病例对照研究旨在评估两组前瞻性队列成人患者感染早期的免疫因素,以预测感染后慢性风湿病(pCHIK-CR)的风险。我们评估了46例发热患者(中位年龄:33.5岁;IQR: 19年;妇女:50.0%),2014-2015年在哥伦比亚桑坦德暴发期间确诊感染了吉kv病毒。参与者由风湿病学家分类为病例(pCHIK-CR)或对照组(WoRM,无风湿病表现)。在感染急性和亚急性期,我们用Luminex和ELISA测定血清中IL-4、IL-6、IL-8/CXCL-8、IL-27、CCL-2、CXCL-9、CXCL-10和IgG的水平。然后,我们利用年龄和性别调整后的分段逻辑回归评估了这些免疫因素与病例对照状态的关联。IL-8/CXCL-8、CXCL-9和CXCL-10与pCHIK-CR呈非线性相关。IL-8/CXCL-8 (
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

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.

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来源期刊
Tropical Medicine and Infectious Disease
Tropical Medicine and Infectious Disease Medicine-Public Health, Environmental and Occupational Health
CiteScore
3.90
自引率
10.30%
发文量
353
审稿时长
11 weeks
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