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The Role of Epstein-Barr Virus in Adults With Bronchiectasis: A Prospective Cohort Study

机译:Epstein-Barr病毒在Bronchiectasis的成人中的作用:一项潜在的队列研究

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BackgroundEpstein-Barr virus (EBV) is implicated in the progression of chronic obstructive pulmonary disease. We aimed to determine whether EBV correlates with bronchiectasis severity, exacerbations, and progression.MethodsWe collected induced sputum in healthy controls and spontaneous sputum at 3–6-month intervals and onset of exacerbations in bronchiectasis patients between March 2017 and October 2018. EBV DNA was detected with quantitative polymerase chain reaction.ResultsWe collected 442 sputum samples from 108 bronchiectasis patients and 50 induced sputum samples from 50 healthy controls. When stable, bronchiectasis patients yielded higher detection rates of EBV DNA (48.1% vs 20.0%; P = .001), but not viral loads (mean log10 load, 4.45 vs 4.76; P = .266), compared with controls; 64.9% of patients yielded consistent detection status between 2 consecutive stable visits. Neither detection rate (40.8% vs 48.1%; P = .393) nor load (mean log10 load, 4.34 vs 4.45; P = .580) differed between the onset of exacerbations and stable visits, nor between exacerbations and convalescence. Neither detection status nor viral loads correlated with bronchiectasis severity. EBV loads correlated negatively with sputum interleukin-1β (P = .002), CXC motif chemokine-8 (P = .008), and tumor necrosis factor–α levels (P = .005). Patients initially detected with, or repeatedly detected with, EBV DNA had significantly faster lung function decline and shorter time to next exacerbations (both P .05) than those without. Detection of EBV DNA was unrelated to influenza virus and opportunistic bacteria (all P .05). The EBV strains detected in bronchiectasis patients were phylogenetically homologous.ConclusionsPatients with detection of EBV DNA have a shorter time to bronchiectasis exacerbations. EBV may contribute to bronchiectasis progression.
机译:Backgroundepstein-Barr病毒(EBV)涉及慢性阻塞性肺病的进展。我们旨在确定EBV是否与支气管扩张严重程度,恶化和进展相关..近期收集了3-6个月间隔的健康对照和自发痰中的痰,并在2017年3月至2018年3月间的支气管扩张患者的恶化发作。EBV DNA是EBV DNA用定量聚合酶链反应检测。从108例支气管扩张患者和50例诱导痰液中收集442个痰样品,来自50例健康对照的50个诱导的痰液样本。当稳定时,支气管扩张患者产生较高的EBV DNA检测率(48.1%Vs 20.0%; p = .001),但不是病毒载荷(平均log10负载,4.45 Vs 4.76; p = .266),与控制相比; 64.9%的患者在2个连续稳定的访问之间产生一致的检测状态。既不检出率(40.8%Vs 48.1%; p = .393)也不是负载(平均log10负载,4.34 vs 4.45; p = .580)不同于加重和稳定的访问,也不会在恶化和康复之间。检测状态既不与支气管扩张严重程度相关。 EBV载荷与痰白细胞介素-1β(P = .002),CXC MOTIF趋化因子-8(p = .008)和肿瘤坏死因子-α水平负相关(p = .005)。最初检测到或反复检测到的患者EBV DNA具有明显更快的肺功能下降和下一步加剧(P <.05)的时间缩短了比没有。 eBV DNA的检测与流感病毒和机会化细菌无关(所有P> .05)。在支气管扩张患者中检测到的EBV菌株是系统源同源的。具有检测的eBV DNA的链致血液,其较短的支气管扩张的加剧时间。 EBV可能有助于支气管扩张进展。

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