Cargando…

Inhibition of HCV 3a genotype entry through Host CD81 and HCV E2 antibodies

BACKGROUND: HCV causes acute and chronic hepatitis which can eventually lead to permanent liver damage hepatocellular carcinoma and death. HCV glycoproteins play an important role in HCV entry by binding with CD81 receptors. Hence inhibition of virus at entry step is an important target to identify...

Descripción completa

Detalles Bibliográficos
Autores principales: Ashfaq, Usman A, Qasim, Muhammad, Yousaf, Muhammad Z, Awan, Muhammad Tariq, Jahan, Shah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228851/
https://www.ncbi.nlm.nih.gov/pubmed/22074322
http://dx.doi.org/10.1186/1479-5876-9-194
_version_ 1782217882742030336
author Ashfaq, Usman A
Qasim, Muhammad
Yousaf, Muhammad Z
Awan, Muhammad Tariq
Jahan, Shah
author_facet Ashfaq, Usman A
Qasim, Muhammad
Yousaf, Muhammad Z
Awan, Muhammad Tariq
Jahan, Shah
author_sort Ashfaq, Usman A
collection PubMed
description BACKGROUND: HCV causes acute and chronic hepatitis which can eventually lead to permanent liver damage hepatocellular carcinoma and death. HCV glycoproteins play an important role in HCV entry by binding with CD81 receptors. Hence inhibition of virus at entry step is an important target to identify antiviral drugs against HCV. METHODS AND RESULT: The present study elaborated the role of CD81 and HCV glycoprotein E2 in HCV entry using retroviral pseudo-particles of 3a local genotype. Our results demonstrated that HCV specific antibody E2 and host antibody CD81 showed dose- dependent inhibition of HCV entry. HCV E2 antibody showed 50% reduction at a concentration of 1.5 ± 1 μg while CD81 exhibited 50% reduction at a concentration of 0.8 ± 1 μg. In addition, data obtained with HCVpp were also confirmed with the infection of whole virus of HCV genotype 3a in liver cells. CONCLUSION: Our data suggest that HCV specific E2 and host CD81 antibodies reduce HCVpp entry and full length viral particle and combination of host and HCV specific antibodies showed synergistic effect in reducing the viral titer.
format Online
Article
Text
id pubmed-3228851
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-32288512011-12-12 Inhibition of HCV 3a genotype entry through Host CD81 and HCV E2 antibodies Ashfaq, Usman A Qasim, Muhammad Yousaf, Muhammad Z Awan, Muhammad Tariq Jahan, Shah J Transl Med Research BACKGROUND: HCV causes acute and chronic hepatitis which can eventually lead to permanent liver damage hepatocellular carcinoma and death. HCV glycoproteins play an important role in HCV entry by binding with CD81 receptors. Hence inhibition of virus at entry step is an important target to identify antiviral drugs against HCV. METHODS AND RESULT: The present study elaborated the role of CD81 and HCV glycoprotein E2 in HCV entry using retroviral pseudo-particles of 3a local genotype. Our results demonstrated that HCV specific antibody E2 and host antibody CD81 showed dose- dependent inhibition of HCV entry. HCV E2 antibody showed 50% reduction at a concentration of 1.5 ± 1 μg while CD81 exhibited 50% reduction at a concentration of 0.8 ± 1 μg. In addition, data obtained with HCVpp were also confirmed with the infection of whole virus of HCV genotype 3a in liver cells. CONCLUSION: Our data suggest that HCV specific E2 and host CD81 antibodies reduce HCVpp entry and full length viral particle and combination of host and HCV specific antibodies showed synergistic effect in reducing the viral titer. BioMed Central 2011-11-10 /pmc/articles/PMC3228851/ /pubmed/22074322 http://dx.doi.org/10.1186/1479-5876-9-194 Text en Copyright ©2011 Ashfaq 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
Ashfaq, Usman A
Qasim, Muhammad
Yousaf, Muhammad Z
Awan, Muhammad Tariq
Jahan, Shah
Inhibition of HCV 3a genotype entry through Host CD81 and HCV E2 antibodies
title Inhibition of HCV 3a genotype entry through Host CD81 and HCV E2 antibodies
title_full Inhibition of HCV 3a genotype entry through Host CD81 and HCV E2 antibodies
title_fullStr Inhibition of HCV 3a genotype entry through Host CD81 and HCV E2 antibodies
title_full_unstemmed Inhibition of HCV 3a genotype entry through Host CD81 and HCV E2 antibodies
title_short Inhibition of HCV 3a genotype entry through Host CD81 and HCV E2 antibodies
title_sort inhibition of hcv 3a genotype entry through host cd81 and hcv e2 antibodies
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228851/
https://www.ncbi.nlm.nih.gov/pubmed/22074322
http://dx.doi.org/10.1186/1479-5876-9-194
work_keys_str_mv AT ashfaqusmana inhibitionofhcv3agenotypeentrythroughhostcd81andhcve2antibodies
AT qasimmuhammad inhibitionofhcv3agenotypeentrythroughhostcd81andhcve2antibodies
AT yousafmuhammadz inhibitionofhcv3agenotypeentrythroughhostcd81andhcve2antibodies
AT awanmuhammadtariq inhibitionofhcv3agenotypeentrythroughhostcd81andhcve2antibodies
AT jahanshah inhibitionofhcv3agenotypeentrythroughhostcd81andhcve2antibodies