VH1-69 gene is preferentially used by hepatitis C virus-associated B cell lymphomas and by normal B cells responding to the E2 viral antigen

被引:144
作者
Chan, CH [1 ]
Hadlock, KG [1 ]
Foung, SKH [1 ]
Levy, S [1 ]
机构
[1] Stanford Univ, Med Ctr, Div Oncol & Pathol, Dept Med, Stanford, CA 94305 USA
关键词
D O I
10.1182/blood.V97.4.1023
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hepatitis C virus (HCV)-associated B cell lymphomas were previously shown to express a restricted repertoire of immunoglobulin V-H and V-L genes, V(H)1-69 and V(K)A27, respectively. Although this suggests a role for antigen selection in the pathogenesis of these lymphomas, the driving antigen involved in the clonal expansion has not been identified. B cell response to a viral antigen, the HCV envelope glycoprotein 2 (E2), was analyzed in an asymptomatic HCV-infected patient. Single B cells, immortalized as hybridomas and selected for binding E2, were analyzed for their V gene usage. Sequences of these V region genes demonstrated that each hybridoma expressed unique V-H and V-L genes. Remarkably, these anti-E2 hybridomas preferentially used the V(H)1-69 gene. Analysis of replacement to silent mutation ratios indicated that the genes underwent somatic mutation and antigenic selection. In a separate report, human anti-E2 antibodies were also shown to express the same V-H gene. These data strengthen the hypothesis that the HCV-associated lymphomas are derived from clonally expanded B cells stimulated by HCV. (C) 2001 by The American Society of Hematology.
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页码:1023 / 1026
页数:4
相关论文
共 40 条
[1]   HEPATITIS-C VIRUS-INFECTION IN TYPE-II MIXED CRYOGLOBULINEMIA [J].
ABEL, G ;
ZHANG, QX ;
AGNELLO, V .
ARTHRITIS AND RHEUMATISM, 1993, 36 (10) :1341-1349
[2]   Recombinant human monoclonal antibodies against different conformational epitopes of the E2 envelope glycoprotein of hepatitis C virus that inhibit its interaction with CD81 [J].
Allander, T ;
Drakenberg, K ;
Beyene, A ;
Rosa, D ;
Abrignani, S ;
Houghton, M ;
Widell, A ;
Grillner, L ;
Persson, MAA .
JOURNAL OF GENERAL VIROLOGY, 2000, 81 :2451-2459
[3]   COMPLETE AMINO-ACID-SEQUENCE OF VARIABLE DOMAINS FROM 2 MONOCLONAL HUMAN ANTI-GAMMA-GLOBULINS OF THE WA CROSS-IDIOTYPIC GROUP - SUGGESTION THAT THE J-SEGMENTS ARE INVOLVED IN THE STRUCTURAL CORRELATE OF THE IDIOTYPE [J].
ANDREWS, DW ;
CAPRA, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (06) :3799-3803
[4]   Aberrant and unstable expression of immunoglobulin genes in persons infected with human immunodeficiency virus [J].
Bessudo, A ;
Rassenti, L ;
Havlir, D ;
Richman, D ;
Feigal, E ;
Kipps, TJ .
BLOOD, 1998, 92 (04) :1317-1323
[5]   Similar characteristics of the CDR3 of VH1-69/DP-10 rearrangements in normal human peripheral blood and chronic lymphocytic leukaemia B cells [J].
Brezinschek, HP ;
Brezinschek, RI ;
Dörner, T ;
Lipsky, PE .
BRITISH JOURNAL OF HAEMATOLOGY, 1998, 102 (02) :516-521
[6]  
BREZINSCHEK HP, 1995, J IMMUNOL, V155, P190
[7]   USE OF FAMILY SPECIFIC LEADER REGION PRIMERS FOR PCR AMPLIFICATION OF THE HUMAN HEAVY-CHAIN VARIABLE REGION GENE REPERTOIRE [J].
CAMPBELL, MJ ;
ZELENETZ, AD ;
LEVY, S ;
LEVY, R .
MOLECULAR IMMUNOLOGY, 1992, 29 (02) :193-203
[8]  
Carroll WL, 1995, ANN NY ACAD SCI, V764, P374
[9]   A COMMON IDIOTOPE ON HUMAN RHEUMATOID FACTORS IDENTIFIED BY A HYBRIDOMA ANTIBODY [J].
CARSON, DA ;
FONG, S .
MOLECULAR IMMUNOLOGY, 1983, 20 (10) :1081-1087
[10]   Molecular virology of hepatitis C virus [J].
Clarke, B .
JOURNAL OF GENERAL VIROLOGY, 1997, 78 :2397-2410