Development of ELISA method for primary detection of HCV using core antigen

Studies show that Hepatitis C Virus (HCV) antigens appear before antibody while the early days of infection. Therefore detecting antigens could lead us to diagnosing the infection on time. The aim of this study was to develop a simple and sensitive enzyme immunoassay for the detection of hepatitis C...

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Main Authors: Nourollahi, Shirin, Boutorabi, Seyed Mehdi, Mirjalili, Ali, Shooshtari, Mahmoud Mahmoudian, Razaghi, Maryam, Hashemi, Masoomeh, Hosseini, Mehrdad Jalalian
Format: Article
Language:English
Published: Marsland Press 2011
Online Access:http://psasir.upm.edu.my/id/eprint/13211/1/Development%20of%20ELISA%20method%20for%20primary%20detection%20of%20HCV%20using%20core%20antigen.pdf
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author Nourollahi, Shirin
Boutorabi, Seyed Mehdi
Mirjalili, Ali
Shooshtari, Mahmoud Mahmoudian
Razaghi, Maryam
Hashemi, Masoomeh
Hosseini, Mehrdad Jalalian
author_facet Nourollahi, Shirin
Boutorabi, Seyed Mehdi
Mirjalili, Ali
Shooshtari, Mahmoud Mahmoudian
Razaghi, Maryam
Hashemi, Masoomeh
Hosseini, Mehrdad Jalalian
author_sort Nourollahi, Shirin
collection UPM
description Studies show that Hepatitis C Virus (HCV) antigens appear before antibody while the early days of infection. Therefore detecting antigens could lead us to diagnosing the infection on time. The aim of this study was to develop a simple and sensitive enzyme immunoassay for the detection of hepatitis C virus (HCV) core antigen in order to evaluate the role of core antigen as a marker of HCV infection. A total of 280 samples was tested by third generation anti-HCV, and the reverse transcription polymerase chain reaction (RT-PCR) was performed only when the anti-HCV enzyme immunoassay (EIA) was positive. All samples were tested with HCV core antigen using Elisa kits. Among the 280 samples, 95 samples were anti-HCV positive. Among those 95 samples, 75 samples were RT-PCR-positive. The cut-off value was set at 0.15 unit of optical density (equivalent to 2.5 pg/ml of core antigen based on the distribution of healthy subjects (anti-HCV-negative subjects). The difference between the mean optical density values of HCV-ribonucleic acid-positive (HCV-RNA-positive) samples and HCV-RNA-negative samples in the HCV core antigen assay was highly significant (1.4 us 0.08, p < 0.005). The sensitivity and specificity of the core antigen assay were 88% and 96%, respectively. The pretreatment of the anti-HCV-positive samples with a solution that contained 1.5 M glycin buffer (pH = 2) increased the sensitivity of the assay (from 57.3% to 88%). This assay is a simple, sensitive, and useful method for use as a screening strategy for HCV infection in anti-HCV-positive or anti-HCV-negative individuals.
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spelling upm.eprints-132112018-06-11T08:44:32Z http://psasir.upm.edu.my/id/eprint/13211/ Development of ELISA method for primary detection of HCV using core antigen Nourollahi, Shirin Boutorabi, Seyed Mehdi Mirjalili, Ali Shooshtari, Mahmoud Mahmoudian Razaghi, Maryam Hashemi, Masoomeh Hosseini, Mehrdad Jalalian Studies show that Hepatitis C Virus (HCV) antigens appear before antibody while the early days of infection. Therefore detecting antigens could lead us to diagnosing the infection on time. The aim of this study was to develop a simple and sensitive enzyme immunoassay for the detection of hepatitis C virus (HCV) core antigen in order to evaluate the role of core antigen as a marker of HCV infection. A total of 280 samples was tested by third generation anti-HCV, and the reverse transcription polymerase chain reaction (RT-PCR) was performed only when the anti-HCV enzyme immunoassay (EIA) was positive. All samples were tested with HCV core antigen using Elisa kits. Among the 280 samples, 95 samples were anti-HCV positive. Among those 95 samples, 75 samples were RT-PCR-positive. The cut-off value was set at 0.15 unit of optical density (equivalent to 2.5 pg/ml of core antigen based on the distribution of healthy subjects (anti-HCV-negative subjects). The difference between the mean optical density values of HCV-ribonucleic acid-positive (HCV-RNA-positive) samples and HCV-RNA-negative samples in the HCV core antigen assay was highly significant (1.4 us 0.08, p < 0.005). The sensitivity and specificity of the core antigen assay were 88% and 96%, respectively. The pretreatment of the anti-HCV-positive samples with a solution that contained 1.5 M glycin buffer (pH = 2) increased the sensitivity of the assay (from 57.3% to 88%). This assay is a simple, sensitive, and useful method for use as a screening strategy for HCV infection in anti-HCV-positive or anti-HCV-negative individuals. Marsland Press 2011 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/13211/1/Development%20of%20ELISA%20method%20for%20primary%20detection%20of%20HCV%20using%20core%20antigen.pdf Nourollahi, Shirin and Boutorabi, Seyed Mehdi and Mirjalili, Ali and Shooshtari, Mahmoud Mahmoudian and Razaghi, Maryam and Hashemi, Masoomeh and Hosseini, Mehrdad Jalalian (2011) Development of ELISA method for primary detection of HCV using core antigen. Journal of American Science, 7 (2). pp. 303-307. ISSN 1545-1003; ESSN: 2375-7264 http://www.jofamericanscience.org/journals/am-sci/am0702/ 10.7537/marsjas070211.38
spellingShingle Nourollahi, Shirin
Boutorabi, Seyed Mehdi
Mirjalili, Ali
Shooshtari, Mahmoud Mahmoudian
Razaghi, Maryam
Hashemi, Masoomeh
Hosseini, Mehrdad Jalalian
Development of ELISA method for primary detection of HCV using core antigen
title Development of ELISA method for primary detection of HCV using core antigen
title_full Development of ELISA method for primary detection of HCV using core antigen
title_fullStr Development of ELISA method for primary detection of HCV using core antigen
title_full_unstemmed Development of ELISA method for primary detection of HCV using core antigen
title_short Development of ELISA method for primary detection of HCV using core antigen
title_sort development of elisa method for primary detection of hcv using core antigen
url http://psasir.upm.edu.my/id/eprint/13211/1/Development%20of%20ELISA%20method%20for%20primary%20detection%20of%20HCV%20using%20core%20antigen.pdf
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