Davison Glen, Schoeman Marlene, Chidley Corinna, Dulson Deborah K, Schweighofer Paul, Witting Christina, Posch Wilfried, Matta Guilherme G, Consoli Claudia, Farley Kyle, McCullough Conor, Wilflingseder Doris
School of Natural Sciences, University of Kent, Kent, UK.
School of Sport and Exercise Science, University of Derby, Derby, UK.
J Physiol. 2025 Mar;603(6):1483-1501. doi: 10.1113/JP288136. Epub 2025 Feb 28.
Upper respiratory tract infection (URTI) has a significant economic and social impact and is a major factor compromising athletes' training and competition. The effects of ColdZyme® Mouth Spray on URTI were investigated using an in vivo study in athletes, combined with a novel in vitro air-liquid interface human airway model. Endurance athletes were randomised to ColdZyme (n = 78) or placebo (n = 76) and monitored over 3 months. They completed daily symptom and training logs and collected throat swabs over 7 days during perceived URTI. In vitro studies examined rhinovirus infectivity and epithelial barrier integrity of airway epithelial cells. Eighty-two in vivo episodes were analysed with significantly lower (P = 0.012) episode duration in the ColdZyme vs. Placebo group (mean ± SD, 6.2 ± 2.6, (median [interquartile range]) 5.5 [4-9] days vs. 10.7 ± 10.2, 7.0 [5-11]). There was no difference in incidence (P = 0.149). Training absence and symptom ratings were lower (P < 0.05) in the ColdZyme group. Swabs were returned for 50 episodes, with at least one pathogen detected in all (rhinovirus was most abundant). Absolute quantification (qPCR) for rhinovirus revealed a significantly lower 7-day area under the curve in ColdZyme vs. placebo (median reduction, 94%, P = 0.029). In vitro, viral load was significantly lower (median reductions 80-100%), and epithelial barrier integrity better maintained, and no virus was detected by immunofluorescence analyses of pseudostratified epithelia, with ColdZyme treatment (all P < 0.05). ColdZyme is beneficial for reducing URTI duration, symptom ratings and missed training days. These novel data suggest that the mechanisms involve the protection of epithelial cells against rhinovirus infection and damage. KEY POINTS: Upper respiratory tract infections (URTI) are a common complaint in the general population and athletes alike, with social, well-being and economic consequences, including performance detriments in athletes and reduced work productivity in the general population. Strategies to minimise the risk of contracting a URTI and/or reduce the time taken to clear an infection are desirable to athletes and the general population alike. The present study employed an in vivo study with athletes in combination with a novel in vitro human airway cell model to examine the effects of ColdZyme Mouth Spray on URTI and viral infectivity. The duration for which URTI symptoms persisted was lower with ColdZyme treatment, which also resulted in fewer training absence days. Swabs from participants in the in vivo study and supernatants from the in vitro studies showed lower rhinovirus viral load with ColdZyme treatment compared with placebo or control.
上呼吸道感染(URTI)具有重大的经济和社会影响,是影响运动员训练和比赛的主要因素。本研究采用运动员体内研究与新型体外气液界面人气道模型相结合的方法,探讨了ColdZyme®口腔喷雾剂对上呼吸道感染的影响。耐力运动员被随机分为ColdZyme组(n = 78)和安慰剂组(n = 76),并进行了3个月的监测。他们每天记录症状和训练情况,并在感觉患上上呼吸道感染的7天内采集咽拭子。体外研究检测了鼻病毒感染性和气道上皮细胞的上皮屏障完整性。对82例体内发病情况进行分析,结果显示ColdZyme组的发病持续时间显著低于安慰剂组(P = 0.012)(平均值±标准差,6.2±2.6,(中位数[四分位间距])5.5[4 - 9]天对10.7±10.2,7.0[5 - 11])。发病率无差异(P = 0.149)。ColdZyme组的训练缺勤率和症状评分较低(P < 0.05)。50例发病情况的咽拭子检测结果显示,所有样本均检测到至少一种病原体(鼻病毒最为常见)。鼻病毒的绝对定量(qPCR)结果显示,ColdZyme组的7天曲线下面积显著低于安慰剂组(中位数降低94%,P = 0.029)。在体外,经ColdZyme处理后,病毒载量显著降低(中位数降低80 - 100%),上皮屏障完整性得到更好维持,假复层上皮的免疫荧光分析未检测到病毒(所有P < 0.05)。ColdZyme有助于缩短上呼吸道感染的持续时间、降低症状评分并减少训练缺勤天数。这些新数据表明,其作用机制包括保护上皮细胞免受鼻病毒感染和损伤。要点:上呼吸道感染在普通人群和运动员中都很常见,会产生社会、健康和经济后果,包括运动员成绩下降和普通人群工作效率降低。对于运动员和普通人群而言,都需要采取策略来降低患上上呼吸道感染的风险和/或缩短感染清除时间。本研究采用运动员体内研究与新型体外人气道细胞模型相结合的方法,研究ColdZyme口腔喷雾剂对上呼吸道感染和病毒感染性的影响。ColdZyme治疗可缩短上呼吸道感染症状持续时间,减少训练缺勤天数。体内研究参与者的咽拭子和体外研究的上清液显示,与安慰剂或对照组相比,ColdZyme治疗组的鼻病毒载量较低。