Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Progress in CRISPR/Cas13-Mediated Suppression of Influenza A and SARS-CoV-2 Virus Infection in in vitro and in vivo Models. / Леонова, Елена Ивановна; Сопова, Юлия Викторовна; Чиринскайте, Ангелина Валерьевна; Решетников, Василий.
в: Biochemistry (Moscow), Том 90, № 6, 01.06.2025, стр. 786–803.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Progress in CRISPR/Cas13-Mediated Suppression of Influenza A and SARS-CoV-2 Virus Infection in in vitro and in vivo Models
AU - Леонова, Елена Ивановна
AU - Сопова, Юлия Викторовна
AU - Чиринскайте, Ангелина Валерьевна
AU - Решетников, Василий
PY - 2025/6/1
Y1 - 2025/6/1
N2 - Abstract: The worldwide number of deaths from complications caused by severe influenza and COVID-19 is about 1 million cases annually. Development of the effective antiviral therapy strategies for the disease treatment is one of the most important tasks. Use of the CRISPR/Cas13 system, which specifically degrades viral RNA and significantly reduces titer of the virus, could be a solution of this problem. Despite the fact that Cas13 nucleases have been discovered only recently, they already have shown high efficiency in suppressing viral transcripts in cell cultures. The recent advances in mRNA technology and improvements in non-viral delivery systems have made it possible to effectively use CRISPR/Cas13 in animal models as well. In this review, we analyzed experimental in vitro and in vivo studies on the use of CRISPR/Cas13 systems as an antiviral agent in cell cultures and animal models and discussed main directions for improving the CRISPR/Cas13 system. These data allow us to understand prospects and limitations of the further use of CRISPR/Cas13 in the treatment of viral diseases.
AB - Abstract: The worldwide number of deaths from complications caused by severe influenza and COVID-19 is about 1 million cases annually. Development of the effective antiviral therapy strategies for the disease treatment is one of the most important tasks. Use of the CRISPR/Cas13 system, which specifically degrades viral RNA and significantly reduces titer of the virus, could be a solution of this problem. Despite the fact that Cas13 nucleases have been discovered only recently, they already have shown high efficiency in suppressing viral transcripts in cell cultures. The recent advances in mRNA technology and improvements in non-viral delivery systems have made it possible to effectively use CRISPR/Cas13 in animal models as well. In this review, we analyzed experimental in vitro and in vivo studies on the use of CRISPR/Cas13 systems as an antiviral agent in cell cultures and animal models and discussed main directions for improving the CRISPR/Cas13 system. These data allow us to understand prospects and limitations of the further use of CRISPR/Cas13 in the treatment of viral diseases.
KW - COVID-19
KW - CRISPR/Cas13
KW - SARS-CoV-2
KW - antiviral drugs
KW - influenza virus
UR - https://www.mendeley.com/catalogue/be93c572-3ecd-3ab6-92e5-a8d437652b64/
U2 - 10.1134/S0006297925601212
DO - 10.1134/S0006297925601212
M3 - Article
VL - 90
SP - 786
EP - 803
JO - Biochemistry (Moscow)
JF - Biochemistry (Moscow)
SN - 0006-2979
IS - 6
ER -
ID: 137814336