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Anti-infectivity of camel polyclonal antibodies against hepatitis C virus in Huh7.5 hepatoma

PURPOSE: To extend the study of the camel milk proteins which have antiviral activity against HCV, camel naïve polyclonal IgGs, α-lactalbumin were purified from camel milk and their anti-HCV effect was examined using PBMCs and Huh7.5 cell-lines. They were compared with the activity of human polyclon...

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Autores principales: EL-Fakharany, Esmail M, Abedelbaky, Nawal, Haroun, Bakry M, Sánchez, Lourdes, Redwan, Nezar A, Redwan, Elrashdy M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583170/
https://www.ncbi.nlm.nih.gov/pubmed/22978304
http://dx.doi.org/10.1186/1743-422X-9-201
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author EL-Fakharany, Esmail M
Abedelbaky, Nawal
Haroun, Bakry M
Sánchez, Lourdes
Redwan, Nezar A
Redwan, Elrashdy M
author_facet EL-Fakharany, Esmail M
Abedelbaky, Nawal
Haroun, Bakry M
Sánchez, Lourdes
Redwan, Nezar A
Redwan, Elrashdy M
author_sort EL-Fakharany, Esmail M
collection PubMed
description PURPOSE: To extend the study of the camel milk proteins which have antiviral activity against HCV, camel naïve polyclonal IgGs, α-lactalbumin were purified from camel milk and their anti-HCV effect was examined using PBMCs and Huh7.5 cell-lines. They were compared with the activity of human polyclonal IgGs and camel lactoferrin and casein. MATERIAL AND METHODS: Three types of experiments were performed on PBMCs and HuH7.5 cell. HCV was directly incubated with the purified proteins and then mixed with both cell types, or the proteins were incubated with the cells and then exposed to HCV, or the HCV pre-infected cells were treated with the proteins to inhibit intracellular replication. The proteins were added to cells or virus at different concentrations and time intervals. RESULTS: Pretreated PBMCs and Huh7.5 cells with milk proteins were not protected when exposed to HCV infection. The direct interaction between HCV and camel IgGs and camel lactoferrin (cLf) led to a complete inhibition of HCV entry into cells, while casein, α-lactalbumin and human IgGs failed to inhibit HCV entry at any tested concentration. Camel IgGs showed ability to recognize HCV peptides with a significant titer (12 × 10(3)) in comparison with human IgGs which failed to do it. Camel lactoferrin was capable of inhibiting the intracellular HCV replication at concentrations of 0.25-1.25 mg/ml. CONCLUSION: Camel milk naïve polyclonal IgGs isolated from camel milk could inhibit the HCV infectivity and demonstrated strong signal against its synthetic peptides. Lactoferrin inhibit the HCV infectivity started from 0.25 mg/ml. However, α-lactalbumin, human IgGs and casein failed to demonstrate any activity against HCV infectivity.
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spelling pubmed-35831702013-02-28 Anti-infectivity of camel polyclonal antibodies against hepatitis C virus in Huh7.5 hepatoma EL-Fakharany, Esmail M Abedelbaky, Nawal Haroun, Bakry M Sánchez, Lourdes Redwan, Nezar A Redwan, Elrashdy M Virol J Research PURPOSE: To extend the study of the camel milk proteins which have antiviral activity against HCV, camel naïve polyclonal IgGs, α-lactalbumin were purified from camel milk and their anti-HCV effect was examined using PBMCs and Huh7.5 cell-lines. They were compared with the activity of human polyclonal IgGs and camel lactoferrin and casein. MATERIAL AND METHODS: Three types of experiments were performed on PBMCs and HuH7.5 cell. HCV was directly incubated with the purified proteins and then mixed with both cell types, or the proteins were incubated with the cells and then exposed to HCV, or the HCV pre-infected cells were treated with the proteins to inhibit intracellular replication. The proteins were added to cells or virus at different concentrations and time intervals. RESULTS: Pretreated PBMCs and Huh7.5 cells with milk proteins were not protected when exposed to HCV infection. The direct interaction between HCV and camel IgGs and camel lactoferrin (cLf) led to a complete inhibition of HCV entry into cells, while casein, α-lactalbumin and human IgGs failed to inhibit HCV entry at any tested concentration. Camel IgGs showed ability to recognize HCV peptides with a significant titer (12 × 10(3)) in comparison with human IgGs which failed to do it. Camel lactoferrin was capable of inhibiting the intracellular HCV replication at concentrations of 0.25-1.25 mg/ml. CONCLUSION: Camel milk naïve polyclonal IgGs isolated from camel milk could inhibit the HCV infectivity and demonstrated strong signal against its synthetic peptides. Lactoferrin inhibit the HCV infectivity started from 0.25 mg/ml. However, α-lactalbumin, human IgGs and casein failed to demonstrate any activity against HCV infectivity. BioMed Central 2012-09-16 /pmc/articles/PMC3583170/ /pubmed/22978304 http://dx.doi.org/10.1186/1743-422X-9-201 Text en Copyright ©2012 EL-Fakharany et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
EL-Fakharany, Esmail M
Abedelbaky, Nawal
Haroun, Bakry M
Sánchez, Lourdes
Redwan, Nezar A
Redwan, Elrashdy M
Anti-infectivity of camel polyclonal antibodies against hepatitis C virus in Huh7.5 hepatoma
title Anti-infectivity of camel polyclonal antibodies against hepatitis C virus in Huh7.5 hepatoma
title_full Anti-infectivity of camel polyclonal antibodies against hepatitis C virus in Huh7.5 hepatoma
title_fullStr Anti-infectivity of camel polyclonal antibodies against hepatitis C virus in Huh7.5 hepatoma
title_full_unstemmed Anti-infectivity of camel polyclonal antibodies against hepatitis C virus in Huh7.5 hepatoma
title_short Anti-infectivity of camel polyclonal antibodies against hepatitis C virus in Huh7.5 hepatoma
title_sort anti-infectivity of camel polyclonal antibodies against hepatitis c virus in huh7.5 hepatoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583170/
https://www.ncbi.nlm.nih.gov/pubmed/22978304
http://dx.doi.org/10.1186/1743-422X-9-201
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