The phenomenon of released-activity. Reply on comment on Don et al.: Dose-dependent antiviral activity of released-active form of antibodies to interferon-gamma against influenza A/California/07/09(H1N1) in murine model

2017 ◽  
Vol 89 (7) ◽  
pp. 1127-1130 ◽  
Author(s):  
Еlena S. Don ◽  
Alexandra G. Emelyanova ◽  
Natalia N. Yakovleva ◽  
Nataliia V. Petrova ◽  
Marina V. Nikiforova ◽  
...  
2016 ◽  
Vol 89 (5) ◽  
pp. 759-766 ◽  
Author(s):  
Еlena S. Don ◽  
Alexandra G. Emelyanova ◽  
Natalia N. Yakovleva ◽  
Nataliia V. Petrova ◽  
Marina V. Nikiforova ◽  
...  

2021 ◽  
Vol 12 (3) ◽  
pp. 727-738
Author(s):  
Jorge L. Arias-Arias ◽  
Francisco Vega-Aguilar ◽  
Dihalá Picado-Soto ◽  
Eugenia Corrales-Aguilar ◽  
Gilbert D. Loría

Zika virus (ZIKV) is a mosquito-borne flavivirus in which human infection became relevant during recent outbreaks in Latin America due to its unrecognized association with fetal neurological disorders. Currently, there are no approved effective antivirals or vaccines for the treatment or prevention of ZIKV infections. Amantadine and rimantadine are approved antivirals used against susceptible influenza A virus infections that have been shown to have antiviral activity against other viruses, such as dengue virus (DENV). Here, we report the in vitro effectiveness of both amantadine and rimantadine hydrochlorides against ZIKV replication, resulting in a dose-dependent reduction in viral titers of a ZIKV clinical isolate and two different ZIKV reference strains. Additionally, we demonstrate similar in vitro antiviral activity of these drugs against DENV-1 and yellow fever virus (YFV), although at higher drug concentrations for the latter. ZIKV replication was inhibited at drug concentrations well below cytotoxic levels of both compounds, as denoted by the high selectivity indexes obtained with the tested strains. Further work is absolutely needed to determine the potential clinical use of these antivirals against ZIKV infections, but our results suggest the existence of a highly conserved mechanism across flavivirus, susceptible to be blocked by modified more specific adamantane compounds.


Author(s):  
Jorge L. Arias-Arias ◽  
Francisco Vega-Aguilar ◽  
Dihalá Picado-Soto ◽  
Eugenia Corrales-Aguilar ◽  
Gilbert D. Loría

Zika virus (ZIKV) is a mosquito-born flavivirus which human infection became relevant dur-ing recent outbreaks in Latin America, due to its unrecognized association with fetal neurologi-cal disorders. Currently there are no approved effective antivirals or vaccines for treatment or prevention of ZIKV infections. Amantadine and rimantadine are approved antivirals used against susceptible influenza A virus infections, that have been shown to have antiviral activity against other viruses, such as dengue virus (DENV). Here, we report the in vitro effectiveness of both amantadine and rimantadine hydrochlorides against ZIKV replication, resulting in a dose-dependent reduction in viral titers of a ZIKV clinical isolate and two different ZIKV refer-ence strains. Additionally, we demonstrate similar in vitro antiviral activity of these drugs against DENV-1 and yellow fever virus (YFV), although at higher drug concentrations for the later. ZIKV replication was inhibited at drug concentrations well below cytotoxic levels of both compounds, as denoted by the high selectivity indexes obtained with the tested strains. Further work is absolutely needed to determine a potential clinical use of these antivirals against ZIKV infections, but our results suggest the existence of a highly conserved mechanism across fla-vivirus, susceptible to be blocked by modified more specific adamantane compounds.


2011 ◽  
Vol 8 (4) ◽  
pp. 375-380 ◽  
Author(s):  
Oleg V. Ardashov ◽  
Vladimir V. Zarubaev ◽  
Anna A. Shtro ◽  
Dina V. Korchagina ◽  
Konstantin P. Volcho ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Yu-Jen Chang ◽  
Cheng-Yun Yeh ◽  
Ju-Chien Cheng ◽  
Yu-Qi Huang ◽  
Kai-Cheng Hsu ◽  
...  

AbstractEradicating influenza A virus (IAV) is difficult, due to its genetic drift and reassortment ability. As the infectious cycle is initiated by the influenza glycoprotein, hemagglutinin (HA), which mediates the binding of virions to terminal sialic acids moieties, HA is a tempting target of anti-influenza inhibitors. However, the complexity of the HA structure has prevented delineation of the structural characterization of the HA protein–ligand complex. Our computational strategy efficiently analyzed > 200,000 records of compounds held in the United States National Cancer Institute (NCI) database and identified potential HA inhibitors, by modeling the sialic acid (SA) receptor binding site (RBS) for the HA structure. Our modeling revealed that compound NSC85561 showed significant antiviral activity against the IAV H1N1 strain with EC50 values ranging from 2.31 to 2.53 µM and negligible cytotoxicity (CC50 > 700 µM). Using the NSC85561 compound as the template to generate 12 derivatives, robust bioassay results revealed the strongest antiviral efficacies with NSC47715 and NSC7223. Virtual screening clearly identified three SA receptor binding site inhibitors that were successfully validated in experimental data. Thus, our computational strategy has identified SA receptor binding site inhibitors against HA that show IAV-associated antiviral activity.


2020 ◽  
Vol 11 ◽  
Author(s):  
Lianci Peng ◽  
Wenjuan Du ◽  
Melanie D. Balhuizen ◽  
Henk P. Haagsman ◽  
Cornelis A. M. de Haan ◽  
...  

2014 ◽  
Vol 5 ◽  
Author(s):  
Emanuel Haasbach ◽  
Carmen Hartmayer ◽  
Alice Hettler ◽  
Alicja Sarnecka ◽  
Ulrich Wulle ◽  
...  

2005 ◽  
Vol 129 (6) ◽  
pp. 1242-1249 ◽  
Author(s):  
Eric M. Sievers ◽  
Robert D. Bart ◽  
Leah M. Backhus ◽  
Yuanguang Lin ◽  
Margaret Starnes ◽  
...  

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