SELECTIVE INTERACTION OF NI WITH AN MHC-BOUND PEPTIDE

被引:124
作者
ROMAGNOLI, P [1 ]
LABHARDT, AM [1 ]
SINIGAGLIA, F [1 ]
机构
[1] F HOFFMANN LA ROCHE & CO LTD,PHARMA RES TECHNOL,CH-4002 BASEL,SWITZERLAND
关键词
ANTIGEN PRESENTATION; HAPTENS; HLA CLASS-II MAJOR HISTOCOMPATIBILITY COMPLEX; NICKEL CONTACT DERMATITIS;
D O I
10.1002/j.1460-2075.1991.tb07648.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
T cells generally recognize foreign antigens as peptides associated with self-molecules encoded by genes of the major histocompatibility complex (MHC). However, T cells which are specific for non-peptidic haptens have been described, in particular in patients with contact sensitivity reactions to metals such as nickel (Ni). Previously, we isolated MHC class II-restricted Ni-specific T cell clones from patients with Ni allergy. The experiments reported here examine the molecular basis for the interaction between Ni and peptide-MHC complexes. We find that Ni alters a T cell response to a peptide and show that Ni interacts with this peptide to alter its antigenicity rather than its ability to bind to MHC molecules. These findings hold implications for a model of hapten recognition by T cells.
引用
收藏
页码:1303 / 1306
页数:4
相关论文
共 23 条
  • [1] BINDING OF IMMUNOGENIC PEPTIDES TO IA HISTOCOMPATIBILITY MOLECULES
    BABBITT, BP
    ALLEN, PM
    MATSUEDA, G
    HABER, E
    UNANUE, ER
    [J]. NATURE, 1985, 317 (6035) : 359 - 361
  • [2] BARANY G, 1980, PEPTIDES, V2, P3
  • [3] THE FOREIGN ANTIGEN-BINDING SITE AND T-CELL RECOGNITION REGIONS OF CLASS-I HISTOCOMPATIBILITY ANTIGENS
    BJORKMAN, PJ
    SAPER, MA
    SAMRAOUI, B
    BENNETT, WS
    STROMINGER, JL
    WILEY, DC
    [J]. NATURE, 1987, 329 (6139) : 512 - 518
  • [4] A HYPOTHETICAL MODEL OF THE FOREIGN ANTIGEN-BINDING SITE OF CLASS-II HISTOCOMPATIBILITY MOLECULES
    BROWN, JH
    JARDETZKY, T
    SAPER, MA
    SAMRAOUI, B
    BJORKMAN, PJ
    WILEY, DC
    [J]. NATURE, 1988, 332 (6167) : 845 - 850
  • [5] CROSS-REACTIVE LYSIS OF TRINITROPHENYL (TNP)-DERIVATIZED H-2 INCOMPATIBLE TARGET-CELLS BY CYTOLYTIC T LYMPHOCYTES GENERATED AGAINST SYNGENEIC TNP SPLEEN-CELLS
    BURAKOFF, SJ
    GERMAIN, RN
    BENACERRAF, B
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1976, 144 (06) : 1609 - 1620
  • [6] AUTOLOGOUS PEPTIDES CONSTITUTIVELY OCCUPY THE ANTIGEN-BINDING SITE ON IA
    BUUS, S
    SETTE, A
    COLON, SM
    GREY, HM
    [J]. SCIENCE, 1988, 242 (4881) : 1045 - 1047
  • [7] THE RELATION BETWEEN MAJOR HISTOCOMPATIBILITY COMPLEX (MHC) RESTRICTION AND THE CAPACITY OF IA TO BIND IMMUNOGENIC PEPTIDES
    BUUS, S
    SETTE, A
    COLON, SM
    MILES, C
    GREY, HM
    [J]. SCIENCE, 1987, 235 (4794) : 1353 - 1358
  • [8] CELL-MEMBRANE ANTIGENS RECOGNIZED BY ANTIVIRALS AND ANTI-TRINITROPHENYL CYTO-TOXIC LYMPHOCYTES-T
    CIAVARRA, R
    FORMAN, J
    [J]. IMMUNOLOGICAL REVIEWS, 1981, 58 : 73 - 94
  • [9] HAPTEN-REACTIVE INDUCER T-CELLS .1. DEFINITION OF 2 CLASSES OF HAPTEN-SPECIFIC INDUCER CELLS
    CLAYBERGER, C
    DEKRUYFF, RH
    AISENBERG, J
    CANTOR, H
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 157 (06) : 1906 - 1919
  • [10] COMPLEX FORMATION BETWEEN METALLIC CATIONS AND PROTEINS, PEPTIDES, AND AMINO ACIDS
    GURD, FRN
    WILCOX, PE
    [J]. ADVANCES IN PROTEIN CHEMISTRY, 1956, 11 : 311 - 427