ANTIBODIES IN HUMAN SERA SPECIFIC TO HYPERVARIABLE REGION-1 OF HEPATITIS-C VIRUS CAN BLOCK VIRAL ATTACHMENT

被引:197
作者
ZIBERT, A [1 ]
SCHREIER, E [1 ]
ROGGENDORF, M [1 ]
机构
[1] ROBERT KOCH INST,W-1000 BERLIN,GERMANY
关键词
D O I
10.1006/viro.1995.1196
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
It has been postulated that antibodies specific to the hypervariable region 1 (HVR1) within the putative envelope protein E2 of hepatitis C virus (HCV) can neutralize virus. We studied such antibodies in sera of patients who were infected in a single-source outbreak by a contaminated anti-D immunoglobulin preparation (HCV-AD78). The nucleotide sequences of cDNAs encoding HVR1 of HCV-AD78 were determined. The four major variants (HVR1.A, B, C, and D) were expressed as fusion proteins in Escherichia coli. Sixty-seven percent of sera contained antibodies to HVR1.A. Sera unrelated to infection of the outbreak also recognized HVR1.A but to a lesser extent (15%), suggesting that not all HVR1-specific antibodies are absolutely isolate-specific. Antibodies directed against individual variants of HVRI were found in sera obtained early postinfection (p.i.) (less than or equal to 1 year) but also in sera obtained several years later. An in vitro binding assay of HCV to tissue culture cells was employed to further characterize these sera. Five of seven sera that were obtained early p.i. prevented binding of HCV to cells. Preincubation of such sera with HVR1-specific fusion proteins restored binding of HCV to cells in four of five sera. These findings suggest that the majority of neutralizing antibodies are directed against HVR1. (C) 1995 Academic Press, Inc.
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页码:653 / 661
页数:9
相关论文
共 42 条
[1]   THE HUMAN BONE-MARROW-DERIVED B-CELL LINE CE, SUSCEPTIBLE TO HEPATITIS-C VIRUS-INFECTION [J].
BERTOLINI, L ;
IACOVACCI, S ;
PONZETTO, A ;
GORINI, G ;
BATTAGLIA, M ;
CARLONI, G .
RESEARCH IN VIROLOGY, 1993, 144 (04) :281-285
[2]   LYMPHOCYTE-T RESPONSE TO HEPATITIS-C VIRUS IN DIFFERENT CLINICAL COURSES OF INFECTION [J].
BOTARELLI, P ;
BRUNETTO, MR ;
MINUTELLO, MA ;
CALVO, P ;
UNUTMAZ, D ;
WEINER, AJ ;
CHOO, QL ;
SHUSTER, JR ;
KUO, G ;
BONINO, F ;
HOUGHTON, M ;
ABRIGNANI, S .
GASTROENTEROLOGY, 1993, 104 (02) :580-587
[3]   AT LEAST 12 GENOTYPES OF HEPATITIS-C VIRUS PREDICTED BY SEQUENCE-ANALYSIS OF THE PUTATIVE E1-GENE OF ISOLATES COLLECTED WORLDWIDE [J].
BUKH, J ;
PURCELL, RH ;
MILLER, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :8234-8238
[4]  
CHIEN DY, 1993, LANCET, V342, P435
[5]   ISOLATION OF A CDNA CLONE DERIVED FROM A BLOOD-BORNE NON-A, NON-B VIRAL-HEPATITIS GENOME [J].
CHOO, QL ;
KUO, G ;
WEINER, AJ ;
OVERBY, LR ;
BRADLEY, DW ;
HOUGHTON, M .
SCIENCE, 1989, 244 (4902) :359-362
[6]   VACCINATION OF CHIMPANZEES AGAINST INFECTION BY THE HEPATITIS-C VIRUS [J].
CHOO, QL ;
KUO, G ;
RALSTON, R ;
WEINER, A ;
CHIEN, D ;
VANNEST, G ;
HAN, J ;
BERGER, K ;
THUDIUM, K ;
KUO, C ;
KANSOPON, J ;
MCFARLAND, J ;
TABRIZI, A ;
CHING, K ;
MOSS, B ;
CUMMINS, LB ;
HOUGHTON, M ;
MUCHMORE, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (04) :1294-1298
[7]   LONG-TERM PERSISTENCE OF HEPATITIS-C VIRUS-ANTIBODIES IN A SINGLE SOURCE OUTBREAK [J].
DITTMANN, S ;
ROGGENDORF, M ;
DURKOP, J ;
WIESE, M ;
LORBEER, B ;
DEINHARDT, F .
JOURNAL OF HEPATOLOGY, 1991, 13 (03) :323-327
[8]   HEPATITIS-C VIRUS (HCV) GENOTYPE DISTRIBUTION IN GERMAN ISOLATES - STUDIES ON THE SEQUENCE VARIABILITY IN THE E2 AND NS5 REGION [J].
DRIESEL, G ;
WIRTH, D ;
STARK, K ;
BAUMGARTEN, R ;
SUCKER, U ;
SCHREIER, E .
ARCHIVES OF VIROLOGY, 1994, 139 (3-4) :379-388
[9]  
ERICKSON AL, 1993, J IMMUNOL, V151, P4189
[10]   HIGH-RATE OF INFECTIVITY AND LIVER-DISEASE IN BLOOD-DONORS WITH ANTIBODIES TO HEPATITIS-C VIRUS [J].
ESTEBAN, JI ;
LOPEZTALAVERA, JC ;
GENESCA, J ;
MADOZ, P ;
VILADOMIU, L ;
MUNIZ, E ;
MARTINVEGA, C ;
ROSELL, M ;
ALLENDE, H ;
VIDAL, X ;
GONZALEZ, A ;
HERNANDEZ, JM ;
ESTEBAN, R ;
GUARDIA, J .
ANNALS OF INTERNAL MEDICINE, 1991, 115 (06) :443-449