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Study of the Humoral Immune Response towards HCV Genotype 4 Using a Bead-Based Multiplex Serological Assay

Hepatitis C is one of the leading causes of hepatocellular carcinoma and remains at a high prevalence in Egypt and other resource-limited countries. Several hepatitis C virus (HCV) genotypes are distributed throughout the world, with genotype 4 being most common in North and Central Africa. We devel...

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Autores principales: Filomena, Angela, Göpfert, Jens C., Duffy, Darragh, Pol, Stanislas, Abdel-Hamid, Mohamed, Esmat, Gamal, Fontanet, Arnaud, Albert, Matthew L., Joos, Thomas O., Schneiderhan-Marra, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748594/
https://www.ncbi.nlm.nih.gov/pubmed/29855459
http://dx.doi.org/10.3390/ht6040015
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author Filomena, Angela
Göpfert, Jens C.
Duffy, Darragh
Pol, Stanislas
Abdel-Hamid, Mohamed
Esmat, Gamal
Fontanet, Arnaud
Albert, Matthew L.
Joos, Thomas O.
Schneiderhan-Marra, Nicole
author_facet Filomena, Angela
Göpfert, Jens C.
Duffy, Darragh
Pol, Stanislas
Abdel-Hamid, Mohamed
Esmat, Gamal
Fontanet, Arnaud
Albert, Matthew L.
Joos, Thomas O.
Schneiderhan-Marra, Nicole
author_sort Filomena, Angela
collection PubMed
description Hepatitis C is one of the leading causes of hepatocellular carcinoma and remains at a high prevalence in Egypt and other resource-limited countries. Several hepatitis C virus (HCV) genotypes are distributed throughout the world, with genotype 4 being most common in North and Central Africa. We developed a multiplex serological assay for the detection of the HCV specific humoral immune response, with a focus on genotype 4. For the multiplex HCV assay we used twelve antigenic regions of different HCV proteins (core, and non-structural (NS) proteins NS3, NS4, NS5A, NS5B) and validated the assay technically and clinically. In comparison to a commercially available test, our assay revealed a higher sensitivity for genotype 4, and is therefore more suited for studying immune seroconversion in samples from acutely infected Egyptian HCV patients. Furthermore, our assay discriminates acutely and chronically infected HCV patients. Of 296 well characterized HCV patient samples, 83.9% of the acute samples and 86.5% of the chronic samples could be correctly classified. In sum, this newly developed serological HCV assay has a higher sensitivity for HCV genotype 4, and can thus improve diagnostic accuracy. Through the discrimination of acutely and chronically infected HCV patients the assay may be useful in supporting clinical management of HCV patients.
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spelling pubmed-57485942018-01-07 Study of the Humoral Immune Response towards HCV Genotype 4 Using a Bead-Based Multiplex Serological Assay Filomena, Angela Göpfert, Jens C. Duffy, Darragh Pol, Stanislas Abdel-Hamid, Mohamed Esmat, Gamal Fontanet, Arnaud Albert, Matthew L. Joos, Thomas O. Schneiderhan-Marra, Nicole High Throughput Article Hepatitis C is one of the leading causes of hepatocellular carcinoma and remains at a high prevalence in Egypt and other resource-limited countries. Several hepatitis C virus (HCV) genotypes are distributed throughout the world, with genotype 4 being most common in North and Central Africa. We developed a multiplex serological assay for the detection of the HCV specific humoral immune response, with a focus on genotype 4. For the multiplex HCV assay we used twelve antigenic regions of different HCV proteins (core, and non-structural (NS) proteins NS3, NS4, NS5A, NS5B) and validated the assay technically and clinically. In comparison to a commercially available test, our assay revealed a higher sensitivity for genotype 4, and is therefore more suited for studying immune seroconversion in samples from acutely infected Egyptian HCV patients. Furthermore, our assay discriminates acutely and chronically infected HCV patients. Of 296 well characterized HCV patient samples, 83.9% of the acute samples and 86.5% of the chronic samples could be correctly classified. In sum, this newly developed serological HCV assay has a higher sensitivity for HCV genotype 4, and can thus improve diagnostic accuracy. Through the discrimination of acutely and chronically infected HCV patients the assay may be useful in supporting clinical management of HCV patients. MDPI 2017-10-30 /pmc/articles/PMC5748594/ /pubmed/29855459 http://dx.doi.org/10.3390/ht6040015 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Filomena, Angela
Göpfert, Jens C.
Duffy, Darragh
Pol, Stanislas
Abdel-Hamid, Mohamed
Esmat, Gamal
Fontanet, Arnaud
Albert, Matthew L.
Joos, Thomas O.
Schneiderhan-Marra, Nicole
Study of the Humoral Immune Response towards HCV Genotype 4 Using a Bead-Based Multiplex Serological Assay
title Study of the Humoral Immune Response towards HCV Genotype 4 Using a Bead-Based Multiplex Serological Assay
title_full Study of the Humoral Immune Response towards HCV Genotype 4 Using a Bead-Based Multiplex Serological Assay
title_fullStr Study of the Humoral Immune Response towards HCV Genotype 4 Using a Bead-Based Multiplex Serological Assay
title_full_unstemmed Study of the Humoral Immune Response towards HCV Genotype 4 Using a Bead-Based Multiplex Serological Assay
title_short Study of the Humoral Immune Response towards HCV Genotype 4 Using a Bead-Based Multiplex Serological Assay
title_sort study of the humoral immune response towards hcv genotype 4 using a bead-based multiplex serological assay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748594/
https://www.ncbi.nlm.nih.gov/pubmed/29855459
http://dx.doi.org/10.3390/ht6040015
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