GlyPerA™ effectively shields airway epithelia from SARS-CoV-2 infection and inflammatory events

被引:4
|
作者
Zaderer, Viktoria [1 ]
Dichtl, Stefanie [1 ]
Posch, Wilfried [1 ]
Abiatari, Ivane [2 ]
Bonn, Guenther K. [3 ]
Jakschitz, Thomas [3 ]
Huber, Lukas A. [3 ,4 ]
Kurzchalia, Teymuras V. [5 ]
Wilflingseder, Doris [1 ]
机构
[1] Med Univ Innsbruck, Inst Hyg & Med Microbiol, Schopfstr 41-R311, A-6020 Innsbruck, Austria
[2] Ilia State Univ, Sch Nat Sci & Med Tbilisi, Tbilisi, Georgia
[3] Austrian Drug Screening Inst ADSI, Innsbruck, Austria
[4] Med Univ Innsbruck, Inst Cell Biol, Bioctr, Innsbruck, Austria
[5] Dzala LLC, 3 Gotua Str, Tbilisi 0160, Georgia
基金
奥地利科学基金会;
关键词
SARS-CoV-2; Prophylaxis; Variants of concern; Antiviral; Transmission;
D O I
10.1186/s12931-023-02397-3
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
New SARS-CoV-2 variants of concern (VOCs) and waning immunity illustrate that quick and easy-to-use agents are needed to prevent infection. To protect from viral transmission and subsequent inflammatory reactions, we applied GlyperA (TM), a novel antimicrobial formulation that can be used as mouth gargling solution or as nasal spray, to highly differentiated human airway epithelia prior infection with Omicron VOCs BA.1 and BA.2. This formulation fully protected polarized human epithelium cultured in air-liquid interphase (ALI) from SARS-CoV-2-mediated tissue destruction and infection upon single application up to two days post infection. Moreover, inflammatory reactions induced by the Omicron VOCs were significantly lowered in tissue equivalents either pre-treated with the GlyperA (TM) solution, or even when added simultaneously. Thus, the GlyperA (TM) formulation significantly shielded epithelial integrity, successfully blocked infection with Omicron and release of viral particles, and decreased intracellular complement C3 activation within human airway epithelial cell cultures. Crucially, our in vitro data imply that GlyperA (TM) may be a simple tool to prevent from SARS-CoV-2 infection independent on the circulating variant via both, mouth and nose.
引用
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页数:9
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