TY - JOUR
T1 - Low cell binding ability of HCV is closely related to interferon treatment especially in patients with HCV genotype 2a/2b
T2 - A large series prospective study on Japanese patients with chronic hepatitis C
AU - Kimura, Yoichi
AU - Hayashida, Kazuhiro
AU - Yanagi, Yusuke
AU - Ishibashi, Hiromi
AU - Akazawa, Kouhei
AU - Niho, Yoshiyuki
N1 - Funding Information:
We thank Dr Yohko K Shimizu for providing us the cell line HPB-Ma and the control plasma, as well as for her helpful discussions We also thank Dr Minako Hijikata for her technical suggestions This work was supported in part by a grant from the Ministry of Education, Science, Sports and Culture of Japan
PY - 2000
Y1 - 2000
N2 - Background/Aims: We have previously shown that the quantity of antibody-free virion in the pre-treatment sera of the patients with chronic hepatitis C is a good predictive factor for the efficacy of interferon treatment. However, the biological significance of the free virion should be verified by a prospective study. Methods: We prospectively evaluated 152 consecutive patients with chronic hepatitis C who received a standardized interferon treatment, and analyzed the free virion and the binding titers, the ability of hepatitis C virus (HCV) to bind to the human lymphocytic cell line. Results: Sixty-five patients achieved a long-term sustained remission, 76 patients did not respond to the interferon therapy, and 11 patients dropped out. The sera from the patients with genotype 2a/2b had significanfly lower free virion and cell binding titers than those with genotype 1b. A multivariate analysis showed three independent variables associated with the interferon response; cell binding titer <100.5/ml, viral load <104.5 copies/50 μl, and genotype 2a/2b with odds ratios of 14.6, 11.8, and 9.8, respectively. Conclusions: The low level of in vitro cell binding ability of HCV helped to clarify the good responsiveness to interferon observed in patients especially with a high viral load of genotype 2a/2b.
AB - Background/Aims: We have previously shown that the quantity of antibody-free virion in the pre-treatment sera of the patients with chronic hepatitis C is a good predictive factor for the efficacy of interferon treatment. However, the biological significance of the free virion should be verified by a prospective study. Methods: We prospectively evaluated 152 consecutive patients with chronic hepatitis C who received a standardized interferon treatment, and analyzed the free virion and the binding titers, the ability of hepatitis C virus (HCV) to bind to the human lymphocytic cell line. Results: Sixty-five patients achieved a long-term sustained remission, 76 patients did not respond to the interferon therapy, and 11 patients dropped out. The sera from the patients with genotype 2a/2b had significanfly lower free virion and cell binding titers than those with genotype 1b. A multivariate analysis showed three independent variables associated with the interferon response; cell binding titer <100.5/ml, viral load <104.5 copies/50 μl, and genotype 2a/2b with odds ratios of 14.6, 11.8, and 9.8, respectively. Conclusions: The low level of in vitro cell binding ability of HCV helped to clarify the good responsiveness to interferon observed in patients especially with a high viral load of genotype 2a/2b.
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U2 - 10.1016/S0168-8278(00)80315-3
DO - 10.1016/S0168-8278(00)80315-3
M3 - Article
C2 - 11097492
AN - SCOPUS:0033768621
SN - 0168-8278
VL - 33
SP - 818
EP - 825
JO - Journal of Hepatology
JF - Journal of Hepatology
IS - 5
ER -