CLINICAL USEFULNESS OF AN ASSAY FOR HEPATITIS-C VIRUS CORE IN THE DIAGNOSIS OF NON-A, NON-B-HEPATITIS AND MONITORING OF THE RESPONSE TO INTERFERON THERAPY
Si. Kawano et al., CLINICAL USEFULNESS OF AN ASSAY FOR HEPATITIS-C VIRUS CORE IN THE DIAGNOSIS OF NON-A, NON-B-HEPATITIS AND MONITORING OF THE RESPONSE TO INTERFERON THERAPY, Journal of gastroenterology and hepatology, 9(3), 1994, pp. 217-222
The clinical utility of a new JCC-2 enzyme-linked immunosorbent assay
kit that detects and quantitates anti-hepatitis C virus (anti-HCV) cor
e antibodies (anti-HCc) was investigated. Serum samples were obtained
from 102 patients with various non-A, non-B liver diseases, including
19 cases of chronic hepatitis type C who had been treated with interfe
ron (IFN). The results of the anti-JCC-2 assay were significantly corr
elated with serum HCV-RNA positivity. Patients who were HCV-RNA positi
ve exhibited a high rate of positivity for anti-JCC-2 (72.2% in acute
hepatitis, > 90% in chronic liver diseases). The geometric mean of the
anti-JCC-2 titre was not significantly different among different stag
es of chronic liver disease (among CPH, CAH and LC). The anti-JCC-2 ti
tre decreased gradually in cases that became HCV-RNA negative after IF
N therapy. If HCV-RNA positivity recurred, the anti-JCC-2 titre increa
sed, indicating that serial measurements of the anti-JCC-2 titre are u
seful for monitoring the antiviral effect of IFN treatment. These resu
lts suggest that quantification of anti-HCc by the anti-JCC-2 assay is
superior to the semi-quantification of circulating HCV-RNA provided b
y monitoring of IFN therapy. Monitoring of HCV-RNA status using revers
e transcription-nested polymerase chain reaction (RT-nested PCR) is po
ssible, but it is technically demanding and too expensive for routine
clinical use.