Vienna Vaccine Safety Initiative, Infectious Diseases & Vaccines, D-10437 Berlin, Germany.
Laboratoire Chrono-Environnement LCE, UMR CNRS 6249, Université Bourgogne Franche-Comté, F-25000 Besançon, France.
Viruses. 2022 Mar 14;14(3):603. doi: 10.3390/v14030603.
Influenza virus (IV) coinfection, i.e., simultaneous infection with IV and other viruses, is a common occurrence in humans. However, little is known about the incidence and clinical impact of coinfection with two different IV subtypes or lineages ("dual infections"). We report the incidence, standardized disease severity, and follow-up of IV dual infections from a hospital-based digital surveillance cohort, comprising 6073 pediatric patients fulfilling pre-defined criteria of influenza-like illness in Berlin, Germany. All patients were tested for IV A/B by PCR, including subtypes/lineages. We assessed all patients at the bedside using the mobile ViVI ScoreApp, providing a validated disease severity score in real-time. IV-positive patients underwent follow-up assessments until resolution of symptoms. Overall, IV dual infections were rare (4/6073 cases; 0.07%, incidence 12/100,000 per year) but showed unusual and/or prolonged clinical presentations with slightly above-average disease severity. We observed viral rebound, serial infection, and B/Yamagata-B/Victoria dual infection. Digital tools, used for instant clinical assessments at the bedside, combined with baseline/follow-up virologic investigation, help identify coinfections in cases of prolonged and/or complicated course of illness. Infection with one IV does not necessarily prevent consecutive or simultaneous (co-/dual) infection, highlighting the importance of multivalent influenza vaccination and enhanced digital clinical and virological surveillance.
流感病毒(IV)合并感染,即同时感染 IV 和其他病毒,在人类中很常见。然而,对于两种不同的 IV 亚型或谱系(“双重感染”)合并感染的发生率和临床影响知之甚少。我们报告了来自基于医院的数字监测队列的 IV 双重感染的发生率、标准化疾病严重程度和随访情况,该队列包括满足德国柏林流感样疾病预定义标准的 6073 例儿科患者。所有患者均通过 PCR 检测 IV A/B,包括亚型/谱系。我们使用移动 ViVI ScoreApp 在床边对所有患者进行评估,实时提供经过验证的疾病严重程度评分。IV 阳性患者接受随访评估,直至症状缓解。总体而言,IV 双重感染很少见(6073 例患者中有 4 例;0.07%,发生率为每年每 100,000 人 12 例),但表现出不寻常和/或延长的临床特征,疾病严重程度略高于平均水平。我们观察到病毒反弹、连续感染和 B/Yamagata-B/Victoria 双重感染。用于床边即时临床评估的数字工具,结合基线/随访病毒学调查,有助于识别延长和/或复杂病程的合并感染。感染一种 IV 并不一定能预防连续或同时(共/双重)感染,这凸显了多价流感疫苗接种和加强数字临床和病毒学监测的重要性。