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**Echinacea Purpurea** for the long-term prevention of viral respiratory tract infections during Covid-19 pandemic : a randomized, open, controlled, exploratory clinical study

Title: **Echinacea Purpurea** for the long-term prevention of viral respiratory tract infections during Covid-19 pandemic : a randomized, open, controlled, exploratory clinical study
Authors: Kolev, Emil; Mircheva, Lilyana; Edwards, Michael R.; Johnston, Sebastian L.; Kalinov, Krassimir; Stange, Rainer; Gancitano, Giuseppe; Vanden Berghe, Wim; Kreft, Samo
Source: 1663-9812 ; Frontiers in pharmacology
Publication Year: 2022
Collection: IRUA - Institutional Repository van de Universiteit Antwerpen
Subject Terms: Pharmacology. Therapy
Description: SARS-CoV-2 vaccination is effective in preventing severe Covid-19, but efficacy in reducing viral load and transmission wanes over time. In addition, the emergence of novel SARS-CoV-2 variants increases the threat of uncontrolled dissemination and additional antiviral therapies are urgently needed for effective containment. In previous in vitro studies Echinacea purpurea demonstrated strong antiviral activity against enveloped viruses, including SARS-CoV-2. In this study, we examined the potential of Echinacea purpurea in preventing and treating respiratory tract infections (RTIs) and in particular, SARS-CoV-2 infections. 120 healthy volunteers (m,f, 18—75 years) were randomly assigned to Echinacea prevention or control group without any intervention. After a run-in week, participants went through 3 prevention cycles of 2, 2 and 1 month with daily 2,400 mg Echinacea purpurea extract (Echinaforce ® , EF). The prevention cycles were interrupted by breaks of 1 week. Acute respiratory symptoms were treated with 4,000 mg EF for up to 10 days, and their severity assessed via a diary. Naso/oropharyngeal swabs and venous blood samples were routinely collected every month and during acute illnesses for detection and identification of respiratory viruses, including SARS-CoV-2 via RT-qPCR and serology. Summarized over all phases of prevention, 21 and 29 samples tested positive for any virus in the EF and control group, of which 5 and 14 samples tested SARS-CoV-2 positive (RR = 0.37, Chi-square test, p = 0.03). Overall, 10 and 14 symptomatic episodes occurred, of which 5 and 8 were Covid-19 (RR = 0.70, Chi-square test, p > 0.05). EF treatment when applied during acute episodes significantly reduced the overall virus load by at least 2.12 log 10 or approx. 99% ( t -test, p < 0.05), the time to virus clearance by 8.0 days for all viruses (Wilcoxon test, p=0.02) and by 4.8 days for SARS-CoV-2 ( p > 0.05) in comparison to control. Finally, EF treatment significantly reduced fever days (1 day vs 11 days, ...
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/isi/000886768300001
Availability: https://hdl.handle.net/10067/1918700151162165141; https://repository.uantwerpen.be/docstore/d:irua:14964
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.678DF0D6
Database: BASE