IDENTIFICATION OF PEPTIDE SEQUENCES THAT POTENTIALLY TRIGGER HLA-A2.1-RESTRICTED CYTOTOXIC T-LYMPHOCYTES

被引:205
作者
NIJMAN, HW
HOUBIERS, JGA
VIERBOOM, MPM
VANDERBURG, SH
DRIJFHOUT, JW
DAMARO, J
KENEMANS, P
MELIEF, CJM
KAST, WM
机构
[1] UNIV HOSP LEIDEN, DEPT IMMUNOHEMATOL, POB 9600, 2300 RC LEIDEN, NETHERLANDS
[2] LEIDEN UNIV HOSP, BLOOD BANK, 2333 AA LEIDEN, NETHERLANDS
[3] FREE UNIV AMSTERDAM HOSP, DEPT OBSTET & GYNECOL, AMSTERDAM, NETHERLANDS
关键词
CYTOTOXIC T-LYMPHOCYTES; INFLUENZA MATRIX PROTEIN; EPITOPE IDENTIFICATION; PROCESSING DEFECTIVE CELL LINE;
D O I
10.1002/eji.1830230603
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We used the human processing defective cell line 174CEM.T2 (T2) to identify potential cytotoxic T lymphocyte (CTL) epitopes of human proteins. Exogenously added peptides can increase the number of properly folded HLA-A2.1 molecules on the cell surface of T2 cells, as shown by immunofluorescence measurements using the mouse monoclonal antibody BB7.2 (anti-HLA-A2.1) and fluorescein isothiocyanate-labeled goat anti-mouse F(ab')2 antibody. The peptides were selected on the basis of a computer score derived from the recently described HLA-A2.1 specific motif. Analysis of the influenza matrix protein showed that 15 out of 35 high-scoring peptides up-regulate the expression of HLA-A2.1 molecules on the T2 cell surface. The combination of the computer scoring program and an immunofluorescence-based peptide binding assay allows rapid detection of potential CTL target peptides.
引用
收藏
页码:1215 / 1219
页数:5
相关论文
共 39 条
  • [1] GENETIC-CONTROL OF HLA-A AND B-ANTIGENS IN SOMATIC-CELL HYBRIDS - REQUIREMENT FOR BETA-2 MICROGLOBULIN
    ARCEGOMEZ, B
    JONES, EA
    BARNSTABLE, CJ
    SOLOMON, E
    BODMER, WF
    [J]. TISSUE ANTIGENS, 1978, 11 (02): : 96 - 112
  • [2] 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
  • [3] SOLUTION BINDING OF AN ANTIGENIC PEPTIDE TO A MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I MOLECULE AND THE ROLE OF BETA-2-MICROGLOBULIN
    BOYD, LF
    KOZLOWSKI, S
    MARGULIES, DH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (06) : 2242 - 2246
  • [4] PRESENTATION OF VIRAL-ANTIGEN CONTROLLED BY A GENE IN THE MAJOR HISTOCOMPATIBILITY COMPLEX
    CERUNDOLO, V
    ALEXANDER, J
    ANDERSON, K
    LAMB, C
    CRESSWELL, P
    MCMICHAEL, A
    GOTCH, F
    TOWNSEND, A
    [J]. NATURE, 1990, 345 (6274) : 449 - 452
  • [5] PEPTIDE LOADING OF EMPTY MAJOR HISTOCOMPATIBILITY COMPLEX-MOLECULES ON RMA-S CELLS ALLOWS THE INDUCTION OF PRIMARY CYTOTOXIC LYMPHOCYTE-T RESPONSES
    DEBRUIJN, MLH
    SCHUMACHER, TNM
    NIELAND, JD
    PLOEGH, HL
    KAST, WM
    MELIEF, CJM
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (12) : 2963 - 2970
  • [6] EFFICIENT PROCESSING OF AN ANTIGENIC SEQUENCE FOR PRESENTATION BY MHC CLASS-I MOLECULES DEPENDS ON ITS NEIGHBORING RESIDUES IN THE PROTEIN
    DELVAL, M
    SCHLICHT, HJ
    RUPPERT, T
    REDDEHASE, MJ
    KOSZINOWSKI, UH
    [J]. CELL, 1991, 66 (06) : 1145 - 1153
  • [7] DeMars R, 1992, Trends Cell Biol, V2, P81, DOI 10.1016/0962-8924(92)90077-Z
  • [8] HOMOZYGOUS DELETIONS THAT SIMULTANEOUSLY ELIMINATE EXPRESSIONS OF CLASS-I AND CLASS-II ANTIGENS OF EBV-TRANSFORMED B-LYMPHOBLASTOID CELLS .1. REDUCED PROLIFERATIVE RESPONSES OF AUTOLOGOUS AND ALLOGENEIC T-CELLS TO MUTANT-CELLS THAT HAVE DECREASED EXPRESSION OF CLASS-II ANTIGENS
    DEMARS, R
    CHANG, CC
    SHAW, S
    REITNAUER, PJ
    SONDEL, PM
    [J]. HUMAN IMMUNOLOGY, 1984, 11 (02) : 77 - 97
  • [9] PREFERRED SIZE OF PEPTIDES THAT BIND TO H-2 KB IS SEQUENCE DEPENDENT
    DERES, K
    SCHUMACHER, TNM
    WIESMULLER, KH
    STEVANOVIC, S
    GREINER, G
    JUNG, G
    PLOEGH, HL
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (06) : 1603 - 1608
  • [10] CELL-FREE SYNTHESIS AND MEMBRANE INSERTION OF MOUSE H-2DD HISTOCOMPATIBILITY ANTIGEN AND BETA-2-MICROGLOBULIN
    DOBBERSTEIN, B
    GAROFF, H
    WARREN, G
    ROBINSON, PJ
    [J]. CELL, 1979, 17 (04) : 759 - 769