基孔肯雅热患者持续关节疼痛的急性免疫学特征和预后生物标志物:系统综述。

IF 2.5 3区 工程技术 Q2 BIOLOGY
Yale Journal of Biology and Medicine Pub Date : 2024-12-19 eCollection Date: 2024-12-01 DOI:10.59249/RQYJ3197
Anyela Lozano-Parra, Víctor Herrera, Silvio Urcuqui-Inchima, Rosa Margarita Gélvez Ramírez, Luis Ángel Villar
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引用次数: 0

摘要

基孔肯雅病毒感染(CHIKV)会增加持续性关节痛的风险;但目前还没有一致的证据表明慢性关节病进展的预后生物标志物。本系统性综述概述了目前可用的文献,这些文献涉及急性免疫反应在预测确诊为 CHIKV 患者的长期关节痛方面的潜在作用。我们在 PubMed/MEDLINE、LILACS、Cochrane Library Plus 和 SCOPUS 数据库中使用 "基孔肯雅病毒"、"细胞因子"、"生物标志物 "和 "关节疼痛 "等词搜索观察性研究,仅限于 2024 年 4 月之前发表的英文文章。PROSPERO 注册号:CRD42021279400。我们选择了 38 项研究进行定性综合,这些研究从诊断到临床评估的最长持续时间为 60 个月。样本量从 8 到 346 人不等(年龄范围:0-90 岁)。我们确定了 CHIKV 急性期的免疫学特征,包括促炎细胞因子(IFN-α、IFN-γ、IL-2R、IL-6、IL-7 和 IL-8)、抗炎细胞因子(IL-1Ra 和 IL-4)、趋化因子(MCP-1、MIG 和 IP-10)和生长因子(VEGF 和 G-CSF)水平的升高。两项研究中只有一项报告了急性期细胞因子水平的差异,预测了 20 个月随访时关节疼痛的持续性。此外,抗CHIKV IgG 的持续存在似乎也是一个潜在的预后标志。这些证据表明,CHIKV 急性期存在炎症反应,并在慢性期持续存在;但是,目前还没有明确的候选生物标志物,可用于预测长期关节后遗症的进展。
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 Profile and Prognostic Biomarkers of Persistent Joint Pain in Chikungunya Fever: A Systematic Review.

Chikungunya virus infection (CHIKV) increases the risk of persistent arthralgia; however, there is no consistent evidence regarding prognostic biomarkers of progression to chronic arthropathy. This systematic review provides an overview of currently available literature about the potential role of the acute immunologic response in predicting long-term joint pain in patients with a diagnosis of CHIKV. We searched for observational studies using the terms "chikungunya," "cytokines," "biomarkers," and "joint pain" in PubMed/MEDLINE, LILACS, Cochrane Library Plus, and SCOPUS databases, restricting to articles published in English and up to April 2024. PROSPERO registration number: CRD42021279400. Thirty-eight studies were selected for qualitative synthesis with a maximum duration from diagnosis to clinical evaluation of 60 months. The sample sizes ranged from 8 to 346 participants (age range: 0-90 years). We identified an immunologic profile during the acute phase of CHIKV that includes increased levels of proinflammatory cytokines (IFN-α, IFN-γ, IL-2R, IL-6, IL-7, and IL-8), anti-inflammatory cytokines (IL-1Ra and IL-4), chemokines (MCP-1, MIG, and IP-10) and growth factors (VEGF and G-CSF). Only one out of two studies reported differences in cytokine levels during the acute phase, predicting persistent joint pain at 20 months of follow-up. Also, persistence of anti-CHIKV IgG seemed to be a potential prognostic marker. The evidence suggests the existence of an inflammatory response in the acute phase of CHIKV that persists during its chronic phase; however, there is no unequivocal candidate set of biomarkers of progression toward long-term articular sequelae.

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来源期刊
Yale Journal of Biology and Medicine
Yale Journal of Biology and Medicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
5.00
自引率
0.00%
发文量
41
期刊介绍: The Yale Journal of Biology and Medicine (YJBM) is a graduate and medical student-run, peer-reviewed, open-access journal dedicated to the publication of original research articles, scientific reviews, articles on medical history, personal perspectives on medicine, policy analyses, case reports, and symposia related to biomedical matters. YJBM is published quarterly and aims to publish articles of interest to both physicians and scientists. YJBM is and has been an internationally distributed journal with a long history of landmark articles. Our contributors feature a notable list of philosophers, statesmen, scientists, and physicians, including Ernst Cassirer, Harvey Cushing, Rene Dubos, Edward Kennedy, Donald Seldin, and Jack Strominger. Our Editorial Board consists of students and faculty members from Yale School of Medicine and Yale University Graduate School of Arts & Sciences. All manuscripts submitted to YJBM are first evaluated on the basis of scientific quality, originality, appropriateness, contribution to the field, and style. Suitable manuscripts are then subject to rigorous, fair, and rapid peer review.
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