Direct evidence that leukemic cells present HLA-associated immunogenic peptides derived from the BCR-ABL b3a2 fusion protein

被引:203
作者
Clark, RE
Dodi, IA
Hill, SC
Lill, JR
Aubert, G
Macintyre, AR
Rojas, J
Bourdon, A
Bonner, PLR
Wang, LH
Christmas, SE
Travers, PJ
Creaser, CS
Rees, RC
Madrigal, JA
机构
[1] Nottingham Trent Univ, Dept Life Sci, Nottingham NG11 8NS, England
[2] Nottingham Trent Univ, Dept Chem, Nottingham NG11 8NS, England
[3] Nottingham Trent Univ, Dept Phys, Nottingham NG11 8NS, England
[4] Univ Liverpool, Dept Haematol & Immunol, Liverpool, Merseyside, England
[5] UCL Royal Free & Univ Coll Med Sch, Anthony Nolan Res Inst, London, England
关键词
D O I
10.1182/blood.V98.10.2887
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The BCR-ABL oncogene is central in the pathogenesis of chronic myeloid leukemia (CML). Here, tandem nanospray mass spectrometry was used to demonstrate cell surface HLA-associated expression of the BCR-ABL peptide KQSSKALQR on class I-negative CIVIL cells transfected with HLA-A*0301, and on primary CIVIL cells from HLA-A3-positive patients. These patients mounted a cytotoxic T-lymphocyte response to KQSSKALQR that also killed autologous CML cells, and tetramer staining demonstrated the presence of circulating KQSSKALQR-specific T cells. The findings are the first demonstration that CML cells express HLA-associated leukemia-specific immunogenic peptides and provide a sound basis for immunization studies against BCR-ABL. (C) 2001 by The American Society of Hematology.
引用
收藏
页码:2887 / 2893
页数:7
相关论文
共 41 条
  • [1] Phenotypic analysis of antigen-specific T lymphocytes
    Altman, JD
    Moss, PAH
    Goulder, PJR
    Barouch, DH
    McHeyzerWilliams, MG
    Bell, JI
    McMichael, AJ
    Davis, MM
    [J]. SCIENCE, 1996, 274 (5284) : 94 - 96
  • [2] [Anonymous], BLOOD
  • [3] IMMUNOLOGICAL CHARACTERIZATION OF THE TUMOR-SPECIFIC BCR ABL JUNCTION OF PHILADELPHIA-CHROMOSOME-POSITIVE CHRONIC MYELOID-LEUKEMIA
    BARRETT, J
    GUIMARAES, A
    CULLIS, J
    GOLDMAN, JM
    [J]. STEM CELLS, 1993, 11 : 104 - 108
  • [4] IN-VITRO PRIMING OF CYTOTOXIC T-LYMPHOCYTES AGAINST POORLY IMMUNOGENIC EPITOPES BY ENGINEERED ANTIGEN-PRESENTING CELLS
    BELLONE, M
    IEZZI, G
    MANFREDI, AA
    PROTTI, MP
    DELLABONA, P
    CASORATI, G
    RUGARLI, C
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (11) : 2691 - 2698
  • [5] Peptides spanning the junctional region of both the abl/bcr and the bcr/abl fusion proteins bind common HLA class I molecules
    Berke, Z
    Andersen, MH
    Pedersen, M
    Fugger, L
    Zeuthen, J
    Haurum, JS
    [J]. LEUKEMIA, 2000, 14 (03) : 419 - 426
  • [6] SPECIFIC BINDING OF LEUKEMIA ONCOGENE FUSION PROTEIN-PEPTIDES TO HLA CLASS-I MOLECULES
    BOCCHIA, M
    WENTWORTH, PA
    SOUTHWOOD, S
    SIDNEY, J
    MCGRAW, K
    SCHEINBERG, DA
    SETTE, A
    [J]. BLOOD, 1995, 85 (10) : 2680 - 2684
  • [7] Specific human cellular immunity to bcr-abl oncogene-derived peptides
    Bocchia, M
    Korontsvit, T
    Xu, Q
    Mackinnon, S
    Yang, SY
    Sette, A
    Scheinberg, DA
    [J]. BLOOD, 1996, 87 (09) : 3587 - 3592
  • [8] Broughton CM, 1997, GENE CHROMOSOME CANC, V18, P292, DOI 10.1002/(SICI)1098-2264(199704)18:4<292::AID-GCC7>3.3.CO
  • [9] 2-I
  • [10] Peptides derived from the whole sequence of BCR-ABL, bind to several class I molecules allowing specific induction of human cytotoxic T lymphocytes
    Buzyn, A
    Ostankovitch, M
    Zerbib, A
    Kemula, M
    Connan, F
    Varet, B
    Guillet, JG
    Choppin, J
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (08) : 2066 - 2072