Development of specific antibodies to an ARF protein in treated patients with chronic HCV infection

被引:30
作者
Cohen, Michal
Bachmatov, Larisa
Ben-Ari, Ziv
Rotman, Yaron
Tur-Kaspa, Ran [1 ]
Zemel, Romy
机构
[1] Beilinson Med Ctr, Rabin Med Ctr, Dept Med D, Petah Tiqwa, Israel
[2] Beilinson Med Ctr, Rabin Med Ctr, Liver Inst, Petah Tiqwa, Israel
[3] Rabin Med Ctr, Mol Hepatol Lab, Felsenstein Med Res Ctr, Petah Tiqwa, Israel
[4] Rabin Med Ctr, Dept Med D, Petah Tiqwa, Israel
[5] Rabin Med Ctr, Liver Inst, Petah Tiqwa, Israel
关键词
hepatitis C virus; HCV core protein; HCVF protein; alternative reading frame protein;
D O I
10.1007/s10620-006-9630-2
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The hepatitis C virus (HCV) F protein is a recently described, frameshift product of HCV core encoding sequence with unknown biological function. In this study we sought to characterize the prevalence of specific anti-F antibodies in patients with chronic HCV infection and to analyze the anti-F antibody profile before, during, and after antiviral treatment in order to gain a better understanding of the role of F protein in HCV pathogenesis. Serum samples were collected from 44 patients with chronic HCV infection and from 19 healthy controls. Consecutive samples from 27 patients taken before, during, and after treatment with antiviral therapy. The F and the core proteins were cloned from the HCV genome. The recombinant proteins were expressed in Escherichia coli and affinity purified. A sensitive and specific enzyme-linked immunosorbent assay was developed to assess the prevalence of anti-F antibodies. Eighty-nine percent of chronic HCV patients had evidence of anti-F antibodies, and 95% of them had anti-core antibodies. No correlation of anti-F antibodies was found with response to treatment, genotype, or seroconversion. We conclude that the F protein elicits specific antibodies in most individuals chronically infected with HCV with no correlation with response to treatment. Our results confirm the expression of F protein during natural HCV infection.
引用
收藏
页码:2427 / 2432
页数:6
相关论文
共 23 条
[1]  
[Anonymous], FIELDS VIROLOGY
[2]   Memory T-cell-mediated immune responses specific to an alternative core protein in hepatitis C virus infection [J].
Bain, C ;
Parroche, P ;
Lavergne, JP ;
Duverger, B ;
Vieux, C ;
Dubois, V ;
Komurian-Pradel, F ;
Trépo, C ;
Gebuhrer, L ;
Paranhos-Baccala, G ;
Penin, F ;
Inchauspé, G .
JOURNAL OF VIROLOGY, 2004, 78 (19) :10460-10469
[3]   RIBOSOMAL FRAMESHIFTING ON VIRAL RNAS [J].
BRIERLEY, I .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :1885-1892
[4]  
Forns X, 1999, Clin Liver Dis, V3, P693, DOI 10.1016/S1089-3261(05)70234-8
[5]   Regulation of interferon regulatory factor-3 by the hepatitis C virus serine protease [J].
Foy, E ;
Li, K ;
Wang, CF ;
Sumpter, R ;
Ikeda, M ;
Lemon, SM ;
Gale, M .
SCIENCE, 2003, 300 (5622) :1145-1148
[6]  
Gosert R, 2002, HEPATOLOGY, V36, p212A
[7]   The HCV core protein acts as a positive regulator of Fas-mediated apoptosis in a human lymphoblastoid T cell line [J].
Hahn, CS ;
Cho, YG ;
Kang, BS ;
Lester, IM ;
Hahn, YS .
VIROLOGY, 2000, 276 (01) :127-137
[8]   THE MEANING AND USE OF THE AREA UNDER A RECEIVER OPERATING CHARACTERISTIC (ROC) CURVE [J].
HANLEY, JA ;
MCNEIL, BJ .
RADIOLOGY, 1982, 143 (01) :29-36
[9]   Hepatitis C virus core protein: Carboxy-terminal boundaries of two processed species suggest cleavage by a signal peptide peptidase [J].
Hussy, P ;
Langen, H ;
Mous, J ;
Jacobsen, H .
VIROLOGY, 1996, 224 (01) :93-104
[10]   Two overlapping reading frames in a single exon encode interacting proteins - a novel way of gene usage [J].
Klemke, M ;
Kehlenbach, RH ;
Huttner, WB .
EMBO JOURNAL, 2001, 20 (14) :3849-3860