Title: Validation of a strategy for HCV antibody testing with two enzyme immunoassays in a routine clinical laboratory
Authors: Vermeersch, Pieter ×
Van Ranst, Marc
Lagrou, Katrien #
Issue Date: Aug-2008
Publisher: Elsevier Science
Series Title: Journal of clinical virology vol:42 issue:4 pages:394-398
Abstract: Background: Centers for Disease Control (CDC) guidelines require confirmation of hepatitis C virus (HCV) screening-test-positive sera with
a low signal/cut-off (S/CO) ratio by recombinant immunoblot or PCR. The UK Health Protection Agency has suggested that a second enzyme
immunoassay (EIA) could be used as an alternative for confirmation in non-immunocompromised patients.
Objective: To evaluate the UK HPA approach in 17,936 consecutive in-house sera submitted for HCV testing.
Study design: AxSYM-positive sera (S/CO≥1.0) were tested with Monolisa Plus. AxSYM-positive sera of patients that were confirmed
PCR-positive were considered HCV+. All other AxSYM-positive sera were confirmed with immunoblot according to CDC guidelines.
Results: 17,299 sera were negative with AxSYM. Of the 637 AxSYM-positive sera, 384 were from patients confirmed as PCR-positive. Of
other 250 sera, 120 were negative with immunoblot, 103 were positive and 30 were indeterminate. All 30 immunoblot-indeterminate sera were
PCR-negative. Two patients were Monolisa Plus+ and immunoblot− and PCR−. One patient was known as immunoblot−, while the other
patientwas diagnosed with non-A non-B hepatitis in 1980s. Nine sera from HCV-positive patients were Monolisa Plus−. Two PCR−sera were
from immunocompetent patients who were PCR− for ≥8 years and six PCR− sera and one PCR+ serum were from immunocompromised
patients. Sensitivity and specificity of confirmation with Monolisa Plus were 98.15% and 98.33% and the positive and negative predictive
values were 99.58% and 92.91% in AxSYM-positive sera (excluding immunoblot-indeterminate/PCR-negative sera). If immunocompromised
patients that were false-negative were excluded, sensitivity was 99.58%.
Conclusion: Monolisa Plus can be used as an alternative to immunoblot for the confirmation of AxSYM-positive sera.
ISSN: 1386-6532
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Laboratory of Clinical Bacteriology and Mycology
Laboratory of Clinical and Epidemiological Virology (Rega Institute)
× corresponding author
# (joint) last author

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