THE BW4 PUBLIC EPITOPE OF HLA-B MOLECULES CONFERS REACTIVITY WITH NATURAL-KILLER-CELL CLONES THAT EXPRESS NKB1, A PUTATIVE HLA RECEPTOR

被引:467
作者
GUMPERZ, JE
LITWIN, V
PHILLIPS, JH
LANIER, LL
PARHAM, P
机构
[1] STANFORD UNIV, DEPT BIOL STRUCT, STANFORD, CA 94305 USA
[2] STANFORD UNIV, DEPT MICROBIOL & IMMUNOL, STANFORD, CA 94305 USA
[3] DNAX RES INST MOLEC & CELLULAR BIOL INC, DEPT HUMAN IMMUNOL, PALO ALTO, CA 94304 USA
关键词
D O I
10.1084/jem.181.3.1133
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although inhibition of natural killer (NK) cell-mediated lysis by the class I HLA molecules of target cells is an established phenomenon, knowledge of the features of class I molecules which induce this effect remains rudimentary. Using class I alleles HLA-B(*)1502 and B(*)1513 which differ only at residues 77-83 which define the Bw4 and Bw6 serological epitopes, we tested the hypothesis that the presence of the Bw4 epitope on class I molecules determines recognition by NKB1(+) NK cells. HLA-B(*)1513 possesses the Bw4 epitope, whereas B(*)1502 has the Bw6 epitope. Lysis by NKB1(+) NK cell clones of transfected target cells expressing B(*)1513 as the only HLA-A, -B, or -C molecule was inhibited, whereas killing of transfectants expressing B(*)1502 was not. Addition of an an anti-NKB1 monoclonal antibody reconstituted lysis of the targets expressing B(*)1513, but did not affect killing of targets bearing B(*)1502. The inhibitory effect of B(*)1513 could be similarly prevented by the addition of an anti-class I monoclonal antibody. These results show that the presence of the Bw4 epitope influences recognition of HLA-B molecules by NK cells that express NKB1, and suggest that the NKB1 molecule may act as a receptor for Bw4(+) HLA-B alleles. Sequences outside of the Bw4 region must also affect recognition by NKB1(+) NK cells, because lysis of transfectants expressing HLA-A(*)2403 or A(*)2501, which possess the Bw4 epitope but are in other ways substantially different from HLA-B molecules, was not increased by addition of the anti-NKB1 antibody. Asparagine 86, the single site of N-linked glycosylation on class I molecules, is in close proximity to the Bw4/Bw6 region. The glycosylation site of the Bw4-positive molecule B(*)5801 was mutated, and the mutant molecules tested for inhibition of NKB1(+) NK cells. Inhibition that could be reversed by addition of the anti-NKB1 monoclonal antibody was observed, showing the presence of the carbohydrate moiety is not essential for class I recognition by NKB1(+) NK cell clones.
引用
收藏
页码:1133 / 1144
页数:12
相关论文
共 52 条
  • [31] GENETIC AND SEROLOGICAL HETEROGENEITY OF THE SUPERTYPIC HLA-B LOCUS SPECIFICITIES BW4 AND BW6
    MULLER, CA
    ENGLERBLUM, G
    GEKELER, V
    STEIERT, I
    WEISS, E
    SCHMIDT, H
    [J]. IMMUNOGENETICS, 1989, 30 (03) : 200 - 207
  • [32] PREVENTION OF ALLOGENEIC BONE-MARROW GRAFT-REJECTION BY H-2 TRANSGENE IN DONOR MICE
    OHLEN, C
    KLING, G
    HOGLUND, P
    HANSSON, M
    SCANGOS, G
    BIEBERICH, C
    JAY, G
    KARRE, K
    [J]. SCIENCE, 1989, 246 (4930) : 666 - 668
  • [33] MONOCLONAL-ANTIBODIES - PURIFICATION, FRAGMENTATION AND APPLICATION TO STRUCTURAL AND FUNCTIONAL-STUDIES OF CLASS-I MHC ANTIGENS
    PARHAM, P
    ANDROLEWICZ, MJ
    BRODSKY, FM
    HOLMES, NJ
    WAYS, JP
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1982, 53 (02) : 133 - 173
  • [34] THE HLA-B73 ANTIGEN HAS A MOST UNUSUAL STRUCTURE THAT DEFINES A 2ND LINEAGE OF HLA-B ALLELES
    PARHAM, P
    ARNETT, KL
    ADAMS, EJ
    BARBER, LD
    DOMENA, JD
    STEWART, D
    HILDEBRAND, WH
    LITTLE, AM
    [J]. TISSUE ANTIGENS, 1994, 43 (05): : 302 - 313
  • [35] PLOEGH HL, 1981, J IMMUNOL, V126, P270
  • [36] THE FREE AND THE BETA-2-MICROGLOBULIN-ASSOCIATED HEAVY-CHAINS OF HLA-A, B ALLOANTIGENS SHARE THE ANTIGENIC DETERMINANT RECOGNIZED BY THE MONOCLONAL-ANTIBODY Q1-28
    QUARANTA, V
    WALKER, LE
    RUBERTO, G
    PELLEGRINO, MA
    FERRONE, S
    [J]. IMMUNOGENETICS, 1981, 13 (04) : 285 - 295
  • [37] RODEY GE, 1987, CRIT REV IMMUNOL, V7, P229
  • [38] ROLSTAD B, 1994, NATURAL IMMUNITY NOR, P99
  • [39] ROTZSCHKE O, 1994, IMMUNOGENETICS, V39, P74
  • [40] AMINO-ACID-SEQUENCES IN THE ALPHA-1 DOMAIN AND NOT GLYCOSYLATION ARE IMPORTANT IN HLA-A2/BETA-2-MICROGLOBULIN ASSOCIATION AND CELL-SURFACE EXPRESSION
    SANTOSAGUADO, J
    BIRO, PA
    FUHRMANN, U
    STROMINGER, JL
    BARBOSA, JA
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (03) : 982 - 990