Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infection

<p>Abstract</p> <p>Background</p> <p>West Nile Virus (WNV) is endemic in Israel and a significant level of antibodies is present in the population due to natural exposure. Anecdotal cases suggested that the presence of anti-WNV antibodies in intravenous immunoglobulin (...

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Main Authors: Gottreich Ahuva, Laub Orgad, Nur Israel, Khinich Yevgeny, Samina Itzchak, Gershoni-Yahalom Orly, Ben-Nathan David, Simanov Michael, Porgador Angel, Rager-Zisman Bracha, Orr Nadav
Format: Article
Language:English
Published: BMC 2009-02-01
Series:BMC Infectious Diseases
Online Access:http://www.biomedcentral.com/1471-2334/9/18
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author Gottreich Ahuva
Laub Orgad
Nur Israel
Khinich Yevgeny
Samina Itzchak
Gershoni-Yahalom Orly
Ben-Nathan David
Simanov Michael
Porgador Angel
Rager-Zisman Bracha
Orr Nadav
author_facet Gottreich Ahuva
Laub Orgad
Nur Israel
Khinich Yevgeny
Samina Itzchak
Gershoni-Yahalom Orly
Ben-Nathan David
Simanov Michael
Porgador Angel
Rager-Zisman Bracha
Orr Nadav
author_sort Gottreich Ahuva
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>West Nile Virus (WNV) is endemic in Israel and a significant level of antibodies is present in the population due to natural exposure. Anecdotal cases suggested that the presence of anti-WNV antibodies in intravenous immunoglobulin (IVIG) from Israeli donors (IVIG-IL) assisted the recovery of patients with severe WNV infection.</p> <p>Methods</p> <p>To enhance the therapeutic efficacy of IVIG-IL against WNV infection, OMRIX Biopharmaceuticals, Israel, have developed a strategy for selection of plasma units from a 10% fraction of Israeli blood donors with anti-WNV antibodies. Positive units were processed into pharmaceutical grade WNV IVIG (WNIG). Following inoculation with WNV, mice received i.p. injections of different doses (0.01–8 mg/mouse) of IVIG-IL or WNIG, according to the specific experimental protocol.</p> <p>Results</p> <p>WNIG was about 10 times more potent (per gr of IgG) than was regular IVIG-IL when tested by ELISA and neutralization assays. In a mouse lethal WNV infection model, prophylactic treatment with WNIG was at least 5–10-fold more potent as compared to treatment with IVIG-IL. Treatment with WNIG during active encephalitis, three or four days following WNV infection, had a significant protective effect. WNIG was also very effective in protecting immunosuppressed mice. Indeed, treatment of dexamethasone-immunosuppressed mice with 0.2 or 1.0 mg WNIG 4 h after virus infection, led to 100% survival.</p> <p>Conclusion</p> <p>IVIG produced from selected plasma donated in WNV endemic regions can be used to produce WNV IVIG with superior activity for therapeutic and prophylactic measures.</p>
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spelling doaj.art-ba4f241482da4bbaac3ab05182e11c412022-12-22T00:10:28ZengBMCBMC Infectious Diseases1471-23342009-02-01911810.1186/1471-2334-9-18Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infectionGottreich AhuvaLaub OrgadNur IsraelKhinich YevgenySamina ItzchakGershoni-Yahalom OrlyBen-Nathan DavidSimanov MichaelPorgador AngelRager-Zisman BrachaOrr Nadav<p>Abstract</p> <p>Background</p> <p>West Nile Virus (WNV) is endemic in Israel and a significant level of antibodies is present in the population due to natural exposure. Anecdotal cases suggested that the presence of anti-WNV antibodies in intravenous immunoglobulin (IVIG) from Israeli donors (IVIG-IL) assisted the recovery of patients with severe WNV infection.</p> <p>Methods</p> <p>To enhance the therapeutic efficacy of IVIG-IL against WNV infection, OMRIX Biopharmaceuticals, Israel, have developed a strategy for selection of plasma units from a 10% fraction of Israeli blood donors with anti-WNV antibodies. Positive units were processed into pharmaceutical grade WNV IVIG (WNIG). Following inoculation with WNV, mice received i.p. injections of different doses (0.01–8 mg/mouse) of IVIG-IL or WNIG, according to the specific experimental protocol.</p> <p>Results</p> <p>WNIG was about 10 times more potent (per gr of IgG) than was regular IVIG-IL when tested by ELISA and neutralization assays. In a mouse lethal WNV infection model, prophylactic treatment with WNIG was at least 5–10-fold more potent as compared to treatment with IVIG-IL. Treatment with WNIG during active encephalitis, three or four days following WNV infection, had a significant protective effect. WNIG was also very effective in protecting immunosuppressed mice. Indeed, treatment of dexamethasone-immunosuppressed mice with 0.2 or 1.0 mg WNIG 4 h after virus infection, led to 100% survival.</p> <p>Conclusion</p> <p>IVIG produced from selected plasma donated in WNV endemic regions can be used to produce WNV IVIG with superior activity for therapeutic and prophylactic measures.</p>http://www.biomedcentral.com/1471-2334/9/18
spellingShingle Gottreich Ahuva
Laub Orgad
Nur Israel
Khinich Yevgeny
Samina Itzchak
Gershoni-Yahalom Orly
Ben-Nathan David
Simanov Michael
Porgador Angel
Rager-Zisman Bracha
Orr Nadav
Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infection
BMC Infectious Diseases
title Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infection
title_full Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infection
title_fullStr Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infection
title_full_unstemmed Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infection
title_short Using high titer West Nile intravenous immunoglobulin from selected Israeli donors for treatment of West Nile virus infection
title_sort using high titer west nile intravenous immunoglobulin from selected israeli donors for treatment of west nile virus infection
url http://www.biomedcentral.com/1471-2334/9/18
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