The Mechanism of Suppression of Chronic Hepatitis C Infection by the Medicine Stimforte
The effect of the drug Stimforte on infection by the Hepatitis C virus (HCV) has been studied. Stimforte partially inhibits HCV infection at a dose of 100 μg/mouse and almost completely at a dose of 300 μg/mouse within 24 h after administration of the drug. The mice sera resulting after 24 h in the...
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Veröffentlicht in: | Biology bulletin of the Russian Academy of Sciences 2020-09, Vol.47 (5), p.448-454 |
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description | The effect of the drug Stimforte on infection by the Hepatitis C virus (HCV) has been studied. Stimforte partially inhibits HCV infection at a dose of 100 μg/mouse and almost completely at a dose of 300 μg/mouse within 24 h after administration of the drug. The mice sera resulting after 24 h in the presence of 100 and 300 µg/mouse of Stimforte effectively inhibit the production of HCV. Doses of 150, 200, and 250 µg/mouse are not effective. Stimulation of interferon-β (IFN-β) production is only observed at doses of 100 and 300 µg/mouse, which explains well the neutralizing capacity of the sera. The amount of IFN-γ also correlates well with the antiviral activity and neutralizing activity of mice sera. The drug practically does not stimulate production of IFN-λ. Thus, the neutralizing activity of sera and the antiviral activity are largely determined by the 1st and 2nd IFN groups. |
doi_str_mv | 10.1134/S1062359020050076 |
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The drug practically does not stimulate production of IFN-λ. Thus, the neutralizing activity of sera and the antiviral activity are largely determined by the 1st and 2nd IFN groups.</description><identifier>ISSN: 1062-3590</identifier><identifier>EISSN: 1608-3059</identifier><identifier>DOI: 10.1134/S1062359020050076</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Antiviral activity ; Biochemistry ; Biomedical and Life Sciences ; Cell Biology ; Chronic infection ; Drug dosages ; Ecology ; Hepatitis ; Hepatitis C ; Infections ; Interferon ; Life Sciences ; Zoology ; β-Interferon ; γ-Interferon</subject><ispartof>Biology bulletin of the Russian Academy of Sciences, 2020-09, Vol.47 (5), p.448-454</ispartof><rights>Pleiades Publishing, Inc. 2020</rights><rights>Pleiades Publishing, Inc. 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c268t-955efaaee372a7bdd41f734735e8266c33c04af04e3f6faf868591d11393896e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S1062359020050076$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1062359020050076$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Mishin, D. 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Stimulation of interferon-β (IFN-β) production is only observed at doses of 100 and 300 µg/mouse, which explains well the neutralizing capacity of the sera. The amount of IFN-γ also correlates well with the antiviral activity and neutralizing activity of mice sera. The drug practically does not stimulate production of IFN-λ. Thus, the neutralizing activity of sera and the antiviral activity are largely determined by the 1st and 2nd IFN groups.</description><subject>Antiviral activity</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Cell Biology</subject><subject>Chronic infection</subject><subject>Drug dosages</subject><subject>Ecology</subject><subject>Hepatitis</subject><subject>Hepatitis C</subject><subject>Infections</subject><subject>Interferon</subject><subject>Life Sciences</subject><subject>Zoology</subject><subject>β-Interferon</subject><subject>γ-Interferon</subject><issn>1062-3590</issn><issn>1608-3059</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kE9Lw0AQxRdRsFY_gLcFz9HZv0mOEtQWKh5a8Ri2m1m7xSZxd3votzexggfxNDO833vDDCHXDG4ZE_JuyUBzoUrgAAog1ydkwjQUmQBVng79IGejfk4uYtwCgBSST8jbaoP0Ge3GtD7uaOfoct_3AWP0XTuO1SZ0rbd0hr1JPvlIKzpvHdo0AusDTd8Bjbe-RbpMfue6kPCSnDnzEfHqp07J6-PDqppli5eneXW_yCzXRcpKpdAZgyhybvJ100jmciFzobDgWlshLEjjQKJw2hlX6EKVrBlOLkVRahRTcnPM7UP3uceY6m23D-2wsuZSgRBMajlQ7EjZ0MUY0NV98DsTDjWDevxf_ed_g4cfPXFg23cMv8n_m74AYRBwow</recordid><startdate>20200901</startdate><enddate>20200901</enddate><creator>Mishin, D. V.</creator><creator>Isaeva, E. I.</creator><creator>Grigorian, S. S.</creator><creator>Balakina, A. A.</creator><creator>Ilyichev, A. V.</creator><creator>Deryabin, P. G.</creator><creator>Maldov, D. G.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20200901</creationdate><title>The Mechanism of Suppression of Chronic Hepatitis C Infection by the Medicine Stimforte</title><author>Mishin, D. V. ; Isaeva, E. I. ; Grigorian, S. S. ; Balakina, A. A. ; Ilyichev, A. V. ; Deryabin, P. G. ; Maldov, D. 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V.</creatorcontrib><creatorcontrib>Deryabin, P. G.</creatorcontrib><creatorcontrib>Maldov, D. G.</creatorcontrib><collection>CrossRef</collection><jtitle>Biology bulletin of the Russian Academy of Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mishin, D. V.</au><au>Isaeva, E. I.</au><au>Grigorian, S. S.</au><au>Balakina, A. A.</au><au>Ilyichev, A. V.</au><au>Deryabin, P. G.</au><au>Maldov, D. G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Mechanism of Suppression of Chronic Hepatitis C Infection by the Medicine Stimforte</atitle><jtitle>Biology bulletin of the Russian Academy of Sciences</jtitle><stitle>Biol Bull Russ Acad Sci</stitle><date>2020-09-01</date><risdate>2020</risdate><volume>47</volume><issue>5</issue><spage>448</spage><epage>454</epage><pages>448-454</pages><issn>1062-3590</issn><eissn>1608-3059</eissn><abstract>The effect of the drug Stimforte on infection by the Hepatitis C virus (HCV) has been studied. Stimforte partially inhibits HCV infection at a dose of 100 μg/mouse and almost completely at a dose of 300 μg/mouse within 24 h after administration of the drug. The mice sera resulting after 24 h in the presence of 100 and 300 µg/mouse of Stimforte effectively inhibit the production of HCV. Doses of 150, 200, and 250 µg/mouse are not effective. Stimulation of interferon-β (IFN-β) production is only observed at doses of 100 and 300 µg/mouse, which explains well the neutralizing capacity of the sera. The amount of IFN-γ also correlates well with the antiviral activity and neutralizing activity of mice sera. The drug practically does not stimulate production of IFN-λ. Thus, the neutralizing activity of sera and the antiviral activity are largely determined by the 1st and 2nd IFN groups.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1062359020050076</doi><tpages>7</tpages></addata></record> |
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subjects | Antiviral activity Biochemistry Biomedical and Life Sciences Cell Biology Chronic infection Drug dosages Ecology Hepatitis Hepatitis C Infections Interferon Life Sciences Zoology β-Interferon γ-Interferon |
title | The Mechanism of Suppression of Chronic Hepatitis C Infection by the Medicine Stimforte |
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