Author: Khaitov, Musa; Nikonova, Alexandra; Shilovskiy, Igor; Kozhikhova, Ksenia; Kofiadi, Ilya; Vishnyakova, Lyudmila; Nikolskii, Alexander; Gattinger, Pia; Kovchina, Valeria; Barvinskaia, Ekaterina; Yumashev, Kirill; Smirnov, Valeriy; Maerle, Artem; Kozlov, Ivan; Shatilov, Artem; Timofeeva, Anastasiia; Andreev, Sergey; Koloskova, Olesya; Kuznetsova, Nadezhda; Vasina, Daria; Nikiforova, Maria; Rybalkin, Sergei; Sergeev, Ilya; Trofimov, Dmitriy; Martynov, Alexander; Berzin, Igor; Gushchin, Vladimir; Kovalchuk, Aleksey; Borisevich, Sergei; Valenta, Rudolf; Khaitov, Rakhim; Skvortsova, Veronica
Title: Silencing of SARSâ€CoVâ€2 with modified siRNAâ€peptide dendrimer formulation Cord-id: 0pxg1zn3 Document date: 2021_5_10
ID: 0pxg1zn3
Snippet: BACKGROUND: First vaccines for prevention of Coronavirus disease 2019 (COVIDâ€19) are becoming available but there is a huge and unmet need for specific forms of treatment. In this study we aimed to evaluate the antiâ€SARSâ€CoVâ€2 effect of siRNA both in vitro and in vivo. METHODS: To identify the most effective molecule out of a panel of 15 in silico designed siRNAs, an in vitro screening system based on vectors expressing SARSâ€CoVâ€2 genes fused with the firefly luciferase reporter gene
Document: BACKGROUND: First vaccines for prevention of Coronavirus disease 2019 (COVIDâ€19) are becoming available but there is a huge and unmet need for specific forms of treatment. In this study we aimed to evaluate the antiâ€SARSâ€CoVâ€2 effect of siRNA both in vitro and in vivo. METHODS: To identify the most effective molecule out of a panel of 15 in silico designed siRNAs, an in vitro screening system based on vectors expressing SARSâ€CoVâ€2 genes fused with the firefly luciferase reporter gene and SARSâ€CoVâ€2â€infected cells was used. The most potent siRNA, siRâ€7, was modified by Locked nucleic acids (LNAs) to obtain siRâ€7â€EM with increased stability and was formulated with the peptide dendrimer KKâ€46 for enhancing cellular uptake to allow topical application by inhalation of the final formulation – siRâ€7â€EM/KKâ€46. Using the Syrian Hamster model for SARSâ€CoVâ€2 infection the antiviral capacity of siRâ€7â€EM/KKâ€46 complex was evaluated. RESULTS: We identified the siRNA, siRâ€7, targeting SARSâ€CoVâ€2 RNAâ€dependent RNA polymerase (RdRp) as the most efficient siRNA inhibiting viral replication in vitro. Moreover, we showed that LNAâ€modification and complexation with the designed peptide dendrimer enhanced the antiviral capacity of siRâ€7 in vitro. We demonstrated significant reduction of virus titer and lung inflammation in animals exposed to inhalation of siRâ€7â€EM/KKâ€46 in vivo. CONCLUSIONS: Thus, we developed a therapeutic strategy for COVIDâ€19 based on inhalation of a modified siRNAâ€peptide dendrimer formulation. The developed medication is intended for inhalation treatment of COVIDâ€19 patients.
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