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 [J].
BABBITT, BP ;
ALLEN, PM ;
MATSUEDA, G ;
HABER, E ;
UNANUE, ER .
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 [J].
BJORKMAN, PJ ;
SAPER, MA ;
SAMRAOUI, B ;
BENNETT, WS ;
STROMINGER, JL ;
WILEY, DC .
NATURE, 1987, 329 (6139) :512-518
[4]   A HYPOTHETICAL MODEL OF THE FOREIGN ANTIGEN-BINDING SITE OF CLASS-II HISTOCOMPATIBILITY MOLECULES [J].
BROWN, JH ;
JARDETZKY, T ;
SAPER, MA ;
SAMRAOUI, B ;
BJORKMAN, PJ ;
WILEY, DC .
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 [J].
BURAKOFF, SJ ;
GERMAIN, RN ;
BENACERRAF, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1976, 144 (06) :1609-1620
[6]   AUTOLOGOUS PEPTIDES CONSTITUTIVELY OCCUPY THE ANTIGEN-BINDING SITE ON IA [J].
BUUS, S ;
SETTE, A ;
COLON, SM ;
GREY, HM .
SCIENCE, 1988, 242 (4881) :1045-1047
[7]   THE RELATION BETWEEN MAJOR HISTOCOMPATIBILITY COMPLEX (MHC) RESTRICTION AND THE CAPACITY OF IA TO BIND IMMUNOGENIC PEPTIDES [J].
BUUS, S ;
SETTE, A ;
COLON, SM ;
MILES, C ;
GREY, HM .
SCIENCE, 1987, 235 (4794) :1353-1358
[8]   CELL-MEMBRANE ANTIGENS RECOGNIZED BY ANTIVIRALS AND ANTI-TRINITROPHENYL CYTO-TOXIC LYMPHOCYTES-T [J].
CIAVARRA, R ;
FORMAN, J .
IMMUNOLOGICAL REVIEWS, 1981, 58 :73-94
[9]   HAPTEN-REACTIVE INDUCER T-CELLS .1. DEFINITION OF 2 CLASSES OF HAPTEN-SPECIFIC INDUCER CELLS [J].
CLAYBERGER, C ;
DEKRUYFF, RH ;
AISENBERG, J ;
CANTOR, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 157 (06) :1906-1919
[10]   COMPLEX FORMATION BETWEEN METALLIC CATIONS AND PROTEINS, PEPTIDES, AND AMINO ACIDS [J].
GURD, FRN ;
WILCOX, PE .
ADVANCES IN PROTEIN CHEMISTRY, 1956, 11 :311-427