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.
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页码:1133 / 1144
页数:12
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共 52 条
  • [1] HLA-B SPECIFICITIES AND W4, W6 SPECIFICITIES ARE ON SAME POLYPEPTIDE
    AYRES, J
    CRESSWELL, P
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1976, 6 (11) : 794 - 799
  • [2] BARBER LD, 1993, ANNU REV CELL BIOL, V9, P163
  • [3] BARNSTABLE CJ, 1979, TISSUE ANTIGENS, V13, P334
  • [4] STRUCTURE OF THE HUMAN CLASS-I HISTOCOMPATIBILITY ANTIGEN, HLA-A2
    BJORKMAN, PJ
    SAPER, MA
    SAMRAOUI, B
    BENNETT, WS
    STROMINGER, JL
    WILEY, DC
    [J]. NATURE, 1987, 329 (6139) : 506 - 512
  • [5] NK3-SPECIFIC NATURAL-KILLER-CELLS ARE SELECTIVELY INHIBITED BY BW4-POSITIVE HLA ALLELES WITH ISOLEUCINE-80
    CELLA, M
    LONGO, A
    FERRARA, GB
    STROMINGER, JL
    COLONNA, M
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (04) : 1235 - 1242
  • [6] CHADWICK BS, 1992, J IMMUNOL, V148, P2307
  • [7] CLAYBERGER C, 1990, J IMMUNOL, V144, P4172
  • [8] GENERATION OF ALLOSPECIFIC NATURAL-KILLER-CELLS BY STIMULATION ACROSS A POLYMORPHISM OF HLA-C
    COLONNA, M
    BROOKS, EG
    FALCO, M
    FERRARA, GB
    STROMINGER, JL
    [J]. SCIENCE, 1993, 260 (5111) : 1121 - 1124
  • [9] DOMENA JD, 1993, TISSUE ANTIGENS, V42, P509
  • [10] PEPTIDE MOTIFS OF HLA-B35 AND HLA-B37 MOLECULES
    FALK, K
    ROTZSCHKE, O
    GRAHOVAC, B
    SCHENDEL, D
    STEVANOVIC, S
    JUNG, G
    RAMMENSEE, HG
    [J]. IMMUNOGENETICS, 1993, 38 (02) : 161 - 162