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Small molecule-based inhibitors for treatment of tick-borne encephalitis virus infection: Nucleoside analogs and nonnucleoside antivirals

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F22%3AN0000251" target="_blank" >RIV/00027162:_____/22:N0000251 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/60077344:_____/22:00569226

  • Výsledek na webu

    <a href="https://www.sciencedirect.com/science/article/abs/pii/S0065774322000033?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/abs/pii/S0065774322000033?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/bs.armc.2022.08.003" target="_blank" >10.1016/bs.armc.2022.08.003</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Small molecule-based inhibitors for treatment of tick-borne encephalitis virus infection: Nucleoside analogs and nonnucleoside antivirals

  • Popis výsledku v původním jazyce

    More than 10,000 people a year become infected with TBEV, in which many cases are fatal. Despite the considerable medical importance of TBE, there is currently no approved antiviral treatment available to cure TBEV infections. Therefore, development of highly efficient and safe anti-TBEV drugs is an urgent medical need. Currently, numerous small molecule-based drugs are used to combat long-lasting/chronic viral infections, including those caused by HIV, HBV, HCV or HSV. Many of these antivirals, showing anti-TBEV activities, could be repurposed for the treatment of TBEV infections. However, it should be noted that small molecule-based treatments of acute viral infection, including TBE, could be somewhat challenging, as the serious/life-threatening symptoms of acute infections are very often a consequence of both viral replication in the host cells/tissues and the proinflammatory immune response combined with cytokine storms. The solution to this problem could be solved by a combination or sequential therapy based on application of both direct-acting antivirals, as well as antiinflammatory agents. Together with effective vaccination strategies specific small molecule-based therapy could provide a potent prophylactic and curative tools to combat human infections caused by TBEV.

  • Název v anglickém jazyce

    Small molecule-based inhibitors for treatment of tick-borne encephalitis virus infection: Nucleoside analogs and nonnucleoside antivirals

  • Popis výsledku anglicky

    More than 10,000 people a year become infected with TBEV, in which many cases are fatal. Despite the considerable medical importance of TBE, there is currently no approved antiviral treatment available to cure TBEV infections. Therefore, development of highly efficient and safe anti-TBEV drugs is an urgent medical need. Currently, numerous small molecule-based drugs are used to combat long-lasting/chronic viral infections, including those caused by HIV, HBV, HCV or HSV. Many of these antivirals, showing anti-TBEV activities, could be repurposed for the treatment of TBEV infections. However, it should be noted that small molecule-based treatments of acute viral infection, including TBE, could be somewhat challenging, as the serious/life-threatening symptoms of acute infections are very often a consequence of both viral replication in the host cells/tissues and the proinflammatory immune response combined with cytokine storms. The solution to this problem could be solved by a combination or sequential therapy based on application of both direct-acting antivirals, as well as antiinflammatory agents. Together with effective vaccination strategies specific small molecule-based therapy could provide a potent prophylactic and curative tools to combat human infections caused by TBEV.

Klasifikace

  • Druh

    C - Kapitola v odborné knize

  • CEP obor

  • OECD FORD obor

    10607 - Virology

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/LTAUSA18016" target="_blank" >LTAUSA18016: Výzkum nových nukleosidových analogů jako antivirotik proti medicínsky významným flavivirům</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2022

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název knihy nebo sborníku

    Annual Reports in Medicinal Chemistry

  • ISBN

    978-0-323-98893-3

  • Počet stran výsledku

    38

  • Strana od-do

    55-92

  • Počet stran knihy

    268

  • Název nakladatele

    Academic Press

  • Místo vydání

    USA, UK

  • Kód UT WoS kapitoly