Clinical consequences of sensitisation to minor histocompatibility antigens before allogeneic bone marrow transplantation

被引:4
作者
Rufer, N
Starobinski, M
Chapuis, B
Gratwohl, A
Jeannet, M
Helg, C
Roosnek, E
机构
[1] Univ Hosp Geneva, Dept Internal Med, Div Immunol, Geneva, Switzerland
[2] Univ Hosp Geneva, Dept Internal Med, Div Hematol, Geneva, Switzerland
[3] Univ Hosp Geneva, Dept Internal Med, Div Oncol, Geneva, Switzerland
[4] Univ Basel Hosp, Div Hematol, CH-4031 Basel, Switzerland
关键词
marrow transplantation; rejection; cytotoxic T lymphocytes; minor histocompatibility antigens;
D O I
10.1038/sj.bmt.1701466
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
To study sensitisation to minor histocompatibility antigens (mHag) before and after BMT, we measured antidonor CTL activity in five patients who had rejected their graft, and in a control group of 10 leukemic patients who engrafted without complications. All patients were transplanted with marrow from an HLA-identical sibling. Fourteen patients were conditioned with cyclophosphamide (120 mg/kg) and TBI (1350 cGy) and received a T cell-depleted graft, while one patient with aplastic anaemia received cyclophosphamide alone and unmanipulated marrow. Before transplantation, anti-donor CTL activity was detected in two of the 15 patients. These patients rejected their grafts at days 21 and 58, respectively. In the other three patients who rejected their grafts at days 41, 60 and 250, CTL activity was found only after transplantation. In contrast, no anti-donor CTLs could be detected at any time in the 10 patients who engrafted permanently. We have identified some of the mHags recognised during graft rejection by cloning and subsequent specificity analysis of the recipient CTLs, In the patient who rejected at day 41 without detectable immunisation before BMT, the response was directed against HA-1, a minor antigen known to play a role in GVHD. In the other combinations, a significant part of the CTL activity was directed against the male antigen H-Y. In the patient who rejected the marrow of her HLA-identical brother at day 250, two clones recognised H-Y, while five others recognised at least three distinct autosomal mHags. This patient had an HLA-identical sister who expressed only one autosomal mHag that had been recognised by one single T cell clone. After re-transplantation with the marrow of this second donor, the CTL activity could no longer be detected and the patient engrafted without further complications.
引用
收藏
页码:895 / 898
页数:4
相关论文
共 24 条
  • [1] ANASETTI C, 1994, BONE MARROW TRANSPL, V13, P693
  • [2] BEATTY PG, 1993, BLOOD, V81, P249
  • [3] MAJOR HISTOCOMPATIBILITY COMPLEX DETERMINES SUSCEPTIBILITY TO CYTOTOXIC T-CELLS DIRECTED AGAINST MINOR HISTOCOMPATIBILITY ANTIGENS
    BEVAN, MJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1975, 142 (06) : 1349 - 1364
  • [4] FERRARA JLM, 1991, NEW ENGL J MED, V324, P667
  • [5] Mismatches of minor histocompatibility antigens between HLA-identical donors and recipients and the development of graft-versus-host disease after bone marrow transplantation
    Goulmy, E
    Schipper, R
    Pool, J
    Blokland, E
    Falkenburg, JHF
    Vossen, J
    Gratwohl, A
    Vogelsang, GB
    vanHouwelingen, HC
    vanRood, JJ
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (05) : 281 - 285
  • [6] GOULMY E, 1991, BONE MARROW TRANSPL, V7, P49
  • [7] GRATWOHL A, 1994, BONE MARROW TRANSPL, V13, P5
  • [8] PRETRANSFUSED PATIENTS WITH SEVERE APLASTIC-ANEMIA EXHIBIT HIGH NUMBERS OF CYTOTOXIC LYMPHOCYTE-T PRECURSORS PROBABLY DIRECTED AT NON-HLA ANTIGENS
    KAMINSKI, ER
    HOWS, JM
    GOLDMAN, JM
    BATCHELOR, JR
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1990, 76 (03) : 401 - 405
  • [9] DEFINITION OF HLA-C ALLELES USING SEQUENCE-SPECIFIC OLIGONUCLEOTIDE PROBES (PCR-SSOP)
    KENNEDY, LJ
    POULTON, KV
    DYER, PA
    OLLIER, WER
    THOMSON, W
    [J]. TISSUE ANTIGENS, 1995, 46 (3-1): : 187 - 195
  • [10] ANALYSIS OF 462 TRANSPLANTATIONS FROM UNRELATED DONORS FACILITATED BY THE NATIONAL-MARROW-DONOR-PROGRAM
    KERNAN, NA
    BARTSCH, G
    ASH, RC
    BEATTY, PG
    CHAMPLIN, R
    FILIPOVICH, A
    GAJEWSKI, J
    HANSEN, JA
    HENSLEEDOWNEY, J
    MCCULLOUGH, J
    MCGLAVE, P
    PERKINS, HA
    PHILLIPS, GL
    SANDERS, J
    STRONCEK, D
    THOMAS, ED
    BLUME, KG
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (09) : 593 - 602