SUPERANTIGENS INTERACT WITH MHC CLASS-II MOLECULES OUTSIDE OF THE ANTIGEN GROOVE

被引:445
作者
DELLABONA, P
PECCOUD, J
KAPPLER, J
MARRACK, P
BENOIST, C
MATHIS, D
机构
[1] FAC MED STRASBOURG,INST CHIM BIOL,CNRS,GENET MOLEC EUCARYOTES LAB,11 RUE HUMANN,F-67085 STRASBOURG,FRANCE
[2] NATL JEWISH HOSP NATL ASTHMA CTR,HOWARD HUGHES MED INST,DENVER,CO 80206
[3] NATL JEWISH HOSP NATL ASTHMA CTR,DEPT MED,DENVER,CO 80206
[4] FAC MED STRASBOURG,INST CHIM BIOL,INSERM,U184,UNITE BIOL MOLEC & GENIE GENET,F-67085 STRASBOURG,FRANCE
基金
美国国家卫生研究院;
关键词
D O I
10.1016/0092-8674(90)90388-U
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
Superantigens, including the staphylococcal enterotoxins and the minor lymphocyte stimulatory antigens, are highly potent immunostimulatory molecules, capable of activating virtually all T cells that express particular T cell receptor (TCR) variable regions. Superantigen stimulation of T lymphocytes depends on major histocompatibility complex (MHC) class II molecules, so there has been some debate as to whether superantigens interact with the antigen binding "groove" on class II complexes, just like conventional peptide antigens, or whether they bind elsewhere and serve as TCR coligands. We compared the presentation of peptide antigens and superantigens by a panel of mutant-presenting cell lines, each displaying an Akα chain with a single alanine replacement along the α helix proposed to form one face of the groove. The negligible effect of these 30 mutations on superantigen presentation, versus their drastic consequences for peptide presentation, prompts us to conclude that superantigens interact with MHC class II molecules outside the groove. © 1990.
引用
收藏
页码:1115 / 1121
页数:7
相关论文
共 53 条
  • [1] Allen P M, 1989, Int Immunol, V1, P141, DOI 10.1093/intimm/1.2.141
  • [2] DIRECT EVIDENCE THAT A CLASS-II MOLECULE AND A SIMPLE GLOBULAR PROTEIN GENERATE MULTIPLE DETERMINANTS
    ALLEN, PM
    MCKEAN, DJ
    BECK, BN
    SHEFFIELD, J
    GLIMCHER, LH
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 162 (04) : 1264 - 1274
  • [3] IDENTIFICATION OF THE T-CELL AND IA CONTACT RESIDUES OF A T-CELL ANTIGENIC EPITOPE
    ALLEN, PM
    MATSUEDA, GR
    EVANS, RJ
    DUNBAR, JB
    MARSHALL, GR
    UNANUE, ER
    [J]. NATURE, 1987, 327 (6124) : 713 - 715
  • [4] ANTIGEN PROCESSING AT THE MOLECULAR-LEVEL
    ALLEN, PM
    [J]. IMMUNOLOGY TODAY, 1987, 8 (09): : 270 - 273
  • [5] ALLEN PM, 1985, J IMMUNOL, V135, P368
  • [6] ANDERSON GD, 1989, J IMMUNOL, V143, P3757
  • [7] ANTIGENIC-COMPETITION AT THE LEVEL OF PEPTIDE-IA BINDING
    BABBITT, BP
    MATSUEDA, G
    HABER, E
    UNANUE, ER
    ALLEN, PM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (12) : 4509 - 4513
  • [8] THE MURINE T-CELL RECEPTOR USES A LIMITED REPERTOIRE OF EXPRESSED V-BETA GENE SEGMENTS
    BARTH, RK
    KIM, BS
    LAN, NC
    HUNKAPILLER, T
    SOBIECK, N
    WINOTO, A
    GERSHENFELD, H
    OKADA, C
    HANSBURG, D
    WEISSMAN, IL
    HOOD, L
    [J]. NATURE, 1985, 316 (6028) : 517 - 523
  • [9] 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
  • [10] 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