<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:type xml:lang="deu">Text</dc:type>
  <dc:type xml:lang="deu">Wissenschaftlicher Artikel</dc:type>
  <dc:format>application/pdf</dc:format>
  <dc:rights xml:lang="eng">© 2025 The Author(s)</dc:rights>
  <dc:rights xml:lang="eng">open access</dc:rights>
  <dc:title xml:lang="eng">ColdZyme® reduces viral load and upper respiratory tract infection duration and protects airway epithelia from infection with human rhinoviruses</dc:title>
  <dc:description xml:lang="eng">Upper respiratory tract infection (URTI) has a significant economic and social impact and is a major factor compromising athletes&#39; 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 &lt; 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 &lt; 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.</dc:description>
  <dc:identifier>doi:10.1113/JP288136</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:source xml:lang="eng">Journal of Physiology</dc:source>
  <dc:publisher>Wiley</dc:publisher>
  <dc:subject xml:lang="eng">Humans</dc:subject>
  <dc:subject xml:lang="eng">Rhinovirus Physiology</dc:subject>
  <dc:subject xml:lang="eng">Male</dc:subject>
  <dc:subject xml:lang="eng">Respiratory Tract Infections Virology</dc:subject>
  <dc:subject xml:lang="eng">Picornaviridae Infections Virology</dc:subject>
  <dc:subject xml:lang="eng">Viral Load</dc:subject>
  <dc:subject xml:lang="eng">Adult</dc:subject>
  <dc:subject xml:lang="eng">Young Adult</dc:subject>
  <dc:subject xml:lang="eng">Respiratory Mucosa Virology</dc:subject>
  <dc:subject xml:lang="eng">Oral Sprays</dc:subject>
  <dc:subject xml:lang="eng">Epithelial Cells Virology</dc:subject>
  <dc:subject xml:lang="eng">Double-Blind Method</dc:subject>
  <dc:subject xml:lang="eng">Athletes</dc:subject>
  <dc:type xml:lang="eng">Text</dc:type>
  <dc:type xml:lang="eng">journal article</dc:type>
  <dc:type xml:lang="ita">Testo</dc:type>
  <dc:type xml:lang="ita">Articolo di rivista</dc:type>
  <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:date>2025</dc:date>
  <dc:creator>Glen Davison</dc:creator>
  <dc:creator>Marlene Schoeman</dc:creator>
  <dc:creator>Corinna Chidley</dc:creator>
  <dc:creator>Deborah K. Dulson</dc:creator>
  <dc:creator>Paul Schweighofer</dc:creator>
  <dc:creator>Christina Witting</dc:creator>
  <dc:creator>Wilfried Posch</dc:creator>
  <dc:creator>Guilherme G. Matta</dc:creator>
  <dc:creator>Claudia Consoli</dc:creator>
  <dc:creator>Kyle Farley</dc:creator>
  <dc:creator>Conor McCullough</dc:creator>
  <dc:creator>Doris Wilflingseder</dc:creator>
  <dc:identifier>https://phaidra.vetmeduni.ac.at/o:4012</dc:identifier>
</oai_dc:dc>