The University of Southampton
University of Southampton Institutional Repository

Therapy-induced clearance of HCV core antigen from plasma predicts an end of treatment viral response

Therapy-induced clearance of HCV core antigen from plasma predicts an end of treatment viral response
Therapy-induced clearance of HCV core antigen from plasma predicts an end of treatment viral response

During viral assembly, viral proteins are released into plasma and can be used to infer viral load. The Architect hepatitis C virus (HCV) core antigen (Ag) assay is a potential alternative to HCV RNA quantification for measuring response to therapy and predicting an end of treatment viral response (EOTR). The HCVp22Ag assay was used to infer viral load in 68 window RNA-containing samples and in 284 samples from baseline to week 14 of ribavirin/interferon treatment in 23 patients with EOTR including three who relapsed, 20 not achieving EOTR and 11 controls. HCV Ag and RNA correlated well (r = 0.86) with linear dose responses on dilution. In patients on therapy and control patients, plasma HCV antigen was detected in 51 of 54 with an interpolated LOD cut off between 10(3) and 10(4) RNA IU/mL. Plasma HCV antigenaemia and plasma RNA levels were significantly different in EOTR from non-EOTR patients at 3 days after treatment start and all times thereafter. Positive and negative EOTR predictive values for HCV RNA >2 log drop and HCV Ag loss at 12 weeks were 70% and 74%, 85% and 93% respectively. HCV Ag reactivity has a linear dose response independent of genotype and correlates well with HCV RNA. The failure to clear HCV Ag is as accurate as the failure to clear HCV RNA at twelve weeks into therapy in predicting the likelihood of failure to achieve EOTR. HCV Ag potentially offers a convenient alternative to RNA measurement for defining a futility flag in HCV therapy.

Antiviral Agents/therapeutic use, Drug Therapy, Combination, Genotype, Hepacivirus/drug effects, Hepatitis C/drug therapy, Hepatitis C Antigens/blood, Humans, Interferon-alpha/therapeutic use, Kaplan-Meier Estimate, Polyethylene Glycols/therapeutic use, Predictive Value of Tests, RNA, Viral/blood, Ribavirin/administration & dosage, Treatment Outcome, Viral Core Proteins/blood, Viral Load
1352-0504
65-71
Tedder, R S
26e3ec06-af79-4131-bcca-bf93c8dadfd5
Tuke, P
d91f4b7f-ed51-4f6f-8a1f-2f2c2e882227
Wallis, N
7261ce6f-1dd8-4e18-911f-b417760bfab7
Wright, M
43325ef9-3459-4c75-b3bf-cf8d8dac2a21
Nicholson, L
d427468f-70bf-4bd9-8f2e-ceebfd159883
Grant, P R
c29f39ec-921e-4e78-9376-57136c344f36
Tedder, R S
26e3ec06-af79-4131-bcca-bf93c8dadfd5
Tuke, P
d91f4b7f-ed51-4f6f-8a1f-2f2c2e882227
Wallis, N
7261ce6f-1dd8-4e18-911f-b417760bfab7
Wright, M
43325ef9-3459-4c75-b3bf-cf8d8dac2a21
Nicholson, L
d427468f-70bf-4bd9-8f2e-ceebfd159883
Grant, P R
c29f39ec-921e-4e78-9376-57136c344f36

Tedder, R S, Tuke, P, Wallis, N, Wright, M, Nicholson, L and Grant, P R (2013) Therapy-induced clearance of HCV core antigen from plasma predicts an end of treatment viral response. Journal of Viral Hepatitis, 20 (1), 65-71. (doi:10.1111/j.1365-2893.2012.01630.x).

Record type: Article

Abstract

During viral assembly, viral proteins are released into plasma and can be used to infer viral load. The Architect hepatitis C virus (HCV) core antigen (Ag) assay is a potential alternative to HCV RNA quantification for measuring response to therapy and predicting an end of treatment viral response (EOTR). The HCVp22Ag assay was used to infer viral load in 68 window RNA-containing samples and in 284 samples from baseline to week 14 of ribavirin/interferon treatment in 23 patients with EOTR including three who relapsed, 20 not achieving EOTR and 11 controls. HCV Ag and RNA correlated well (r = 0.86) with linear dose responses on dilution. In patients on therapy and control patients, plasma HCV antigen was detected in 51 of 54 with an interpolated LOD cut off between 10(3) and 10(4) RNA IU/mL. Plasma HCV antigenaemia and plasma RNA levels were significantly different in EOTR from non-EOTR patients at 3 days after treatment start and all times thereafter. Positive and negative EOTR predictive values for HCV RNA >2 log drop and HCV Ag loss at 12 weeks were 70% and 74%, 85% and 93% respectively. HCV Ag reactivity has a linear dose response independent of genotype and correlates well with HCV RNA. The failure to clear HCV Ag is as accurate as the failure to clear HCV RNA at twelve weeks into therapy in predicting the likelihood of failure to achieve EOTR. HCV Ag potentially offers a convenient alternative to RNA measurement for defining a futility flag in HCV therapy.

This record has no associated files available for download.

More information

Published date: 1 January 2013
Additional Information: © 2012 Blackwell Publishing Ltd.
Keywords: Antiviral Agents/therapeutic use, Drug Therapy, Combination, Genotype, Hepacivirus/drug effects, Hepatitis C/drug therapy, Hepatitis C Antigens/blood, Humans, Interferon-alpha/therapeutic use, Kaplan-Meier Estimate, Polyethylene Glycols/therapeutic use, Predictive Value of Tests, RNA, Viral/blood, Ribavirin/administration & dosage, Treatment Outcome, Viral Core Proteins/blood, Viral Load

Identifiers

Local EPrints ID: 478089
URI: http://eprints.soton.ac.uk/id/eprint/478089
ISSN: 1352-0504
PURE UUID: 476fb0e5-3642-4992-a538-2c449855a3c0

Catalogue record

Date deposited: 21 Jun 2023 16:54
Last modified: 17 Mar 2024 02:13

Export record

Altmetrics

Contributors

Author: R S Tedder
Author: P Tuke
Author: N Wallis
Author: M Wright
Author: L Nicholson
Author: P R Grant

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×