THE GENETIC-BASIS OF HUMAN VH4 GENE FAMILY-ASSOCIATED CROSS-REACTIVE IDIOTYPE EXPRESSION IN CD5+ AND CD5- CORD-BLOOD B-LYMPHOCYTE CLONES

被引:16
作者
DEANE, M
MACKENZIE, LE
STEVENSON, FK
YOUINOU, PY
LYDYARD, PM
MAGEED, RA
机构
[1] KENNEDY INST, 6 BUTE GARDENS, HAMMERSMITH, LONDON W6 7DW, ENGLAND
[2] ROYAL FREE HOSP, DEPT HEMATOL, LONDON, ENGLAND
[3] UNIV COLL & MIDDLESEX SCH MED, DEPT IMMUNOL, LONDON, ENGLAND
[4] SOUTHAMPTON GEN HOSP, TENOVUS RES LAB, SOUTHAMPTON SO9 4XY, HANTS, ENGLAND
[5] UNIV BREST, DEPT IMMUNOL, BREST, FRANCE
关键词
D O I
10.1111/j.1365-3083.1993.tb01737.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In a recent study we have observed a high frequency expression of cross-reactive idiotypes encoded by genes from the relatively small V(H)4 family of immunoglobulin heavy chain genes in cord blood B-lymphocyte lines. Furthermore, we have demonstrated a selective pattern of expression of two V(H)4-associated cross-reactive idiotype (CRI) in B-lymphocyte lines established from CD5+ and CD5- cord blood B-lymphocytes. There was a restricted expression of one CRI marker recognized by the 9G4 monoclonal antibody in lines established from CD5+ B-lymphocytes but not in those established from the CD5- population. In the current study we examine the molecular basis for the selective pattern of CRI expression. Nucleotide-sequence analysis of functional immunoglobulin heavy chain (IgH) gene rearrangements in three CD5 + lines expressing the CRI recognised by 9G4 reveal that all use a single gene from the V(H)4 family, the V4.21 gene. However, all three lines have distinct third complementarity determining regions (CDR3) implying different clonal origins. In contrast, four cord blood cell lines (two established from CD5+ B-lymphocytes) expressing the CRI recognized by MoAb Lcl have functional IgH gene rearrangements involving two different genes from the V(H)4 family, the V71-4, and V2-1 genes. Antigen specificity analysis reveals that all three 9G4-reactive lines produce antibodies that react with the I and/or i red blood cell carbohydrate antigens. These data suggest that the distinction in V(H)4 gene use in CD5+ B-lymphocytes in cord blood results from a selection process in vivo that shapes the repertoire of CD5+ B-lymphocytes. This study extends recent observations that the monoclonal anti-CRI antibodies 9G4 and Lc1 are markers of two distinct subgroups of proteins encoded by two subsets of genes within the V(H)4 family. Furthermore, it appears that amino acid residues in framework region one and complementarity determining region two are critical for the expression of the cross reactive idiotypes and the serological distinction between the two subgroups of proteins.
引用
收藏
页码:348 / 358
页数:11
相关论文
共 65 条
[1]   REGULATION OF GENOME REARRANGEMENT EVENTS DURING LYMPHOCYTE DIFFERENTIATION [J].
ALT, FW ;
BLACKWELL, TK ;
DEPINHO, RA ;
RETH, MG ;
YANCOPOULOS, GD .
IMMUNOLOGICAL REVIEWS, 1986, 89 :5-30
[2]  
ANTIN JH, 1986, J IMMUNOL, V136, P505
[3]  
BAHLER DW, 1991, BLOOD, V78, P1561
[4]   CONTENT AND ORGANIZATION OF THE HUMAN IG VH LOCUS - DEFINITION OF 3 NEW VH FAMILIES AND LINKAGE TO THE IG CH LOCUS [J].
BERMAN, JE ;
MELLIS, SJ ;
POLLOCK, R ;
SMITH, CL ;
SUH, H ;
HEINKE, B ;
KOWAL, C ;
SURTI, U ;
CHESS, L ;
CANTOR, CR ;
ALT, FW .
EMBO JOURNAL, 1988, 7 (03) :727-738
[5]  
BOFILL M, 1985, J IMMUNOL, V134, P1531
[6]  
BROWN CMS, 1992, CLIN EXP IMMUNOL, V89, P230
[7]   THE USE OF CHROMOSOMAL TRANSLOCATIONS TO STUDY HUMAN-IMMUNOGLOBULIN GENE ORGANIZATION - MAPPING DH SEGMENTS WITHIN 35 KB OF THE C-MU GENE AND IDENTIFICATION OF A NEW DH LOCUS [J].
BULUWELA, L ;
ALBERTSON, DG ;
SHERRINGTON, P ;
RABBITTS, PH ;
SPURR, N ;
RABBITTS, TH .
EMBO JOURNAL, 1988, 7 (07) :2003-2010
[8]   INFREQUENT NORMAL LYMPHOCYTES-B EXPRESS FEATURES OF B-CHRONIC LYMPHOCYTIC-LEUKEMIA [J].
CALIGARISCAPPIO, F ;
GOBBI, M ;
BOFILL, M ;
JANOSSY, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 155 (02) :623-628
[9]  
CASALI P, 1989, ANNU REV IMMUNOL, V7, P513, DOI 10.1146/annurev.iy.07.040189.002501
[10]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299