LiveSpo® Navax probiotics that contain Bacillus spores effectively support symptomatic treatment and reduce the concentration of respiratory syncytial virus (RSV) in children

Trần Thanh Tú, Nguyễn Thị Vân Anh, Phùng Thị Bích Thủy, Bùi Thị Huyền, Nguyễn Thị Thanh Phúc, Vũ Thị Tâm, Ngô Thị Phương Nga, Nguyễn Thị Mai, Đỗ Thị Hậu, Ngô Hồng Thủy, Phạm Thị Thu Trang, Lê Xuân Ngọc, Đỗ Thu Hường, Nguyễn Hòa Anh

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Abstract

Background/Aims: Infection with the Respiratory Syncytial Virus (RSV) is one of the most common causes of respiratory tract diseases. This study was conducted to initially investigate supportive therapeutic effects of probiotic product LiveSpo® Navax, as liquid form containing Bacilus spores of LS-III generation at a high concentration, in children having acute respiratory diseases caused by RSV at the Vietnam National Children’s Hospital. Methods: Totally 30 patients acquiring bronchiolitis
participated in the blind clinical study. The patients were divided randomly into 2 groups (n = 15/group each): one using LiveSpo® Navax (Navax group) and the other using 0.9% NaCl physiological saline (Control group), and were instructed to perform nasal spraying at frequency of 3 times per day for continuous 6 days, in combination with conventional drug therapy in the hospital. The patients were monitored their clinical indicators throughout the treatment period and underwent tests such
as: (i) RSV rapid test at day 0, quantitative analysis of RSV, B. subtilis and B. clausii concentrations in nasal wash sample at day 0 and day 3 by real-time PCR. Results: The Navax group had about 1-day shorter recovery time of symptoms such as nasal secretion, dificutly breathing, sonorous rales, moist rales, chest depression than the control group. After 3 days of treatment, the Navax group had about 300-fold reduced RSV concentration in their nasal fluid, while the control group had only 15-fold
reduction; in association with the presence of B. subtilis and B. clausii in the nasal fluids of Navax group but absence in Control group. 100% of patients using LiveSpo® Navax showed neither signs of abnormal breath, pulse, irritation of the nasal mucosa, nor digestion. Conclusion: This study is the first clinical trial in chidren in the world to demonstrate safety and effects of Bacillus spore probiotics as nasal spray. LiveSpo® Navax provided 1-day earlier treatment time of typtical symptoms for respiratory diseases caused by RSV infection, as well as effectively reduced the concentration of RSV in nasal fluid of children by 20-fold higher than 0.9% NaCl physiological saline.

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