Hematopoietic lineage-restricted minor histocompatibility antigen HA-1 in graft-versus-leukemia activity after donor lymphocyte infusion

被引:16
|
作者
Kircher, B
Wolf, M
Stevanovic, S
Rammensee, HG
Grubeck-Loebenstein, B
Gastl, G
Nachbaur, D
机构
[1] Univ Innsbruck Hosp, Lab Tumor & Immunobiol, Div Hematol & Oncol, Dept Internal Med,Bone Marrow Transplant Unit, A-6020 Innsbruck, Austria
[2] Austrian Acad Sci, Inst Biomed Aging Res, Innsbruck, Austria
[3] Univ Tubingen, Inst Cellular Biol, Dept Immunol, D-72074 Tubingen, Germany
来源
JOURNAL OF IMMUNOTHERAPY | 2004年 / 27卷 / 02期
关键词
D O I
10.1097/00002371-200403000-00009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunocompetent alloreactive donor lymphocytes directed against minor histocompatibility antigens are supposed to be responsible for graft-versus-host disease (GvHD) and graft-versus-leukemia (GvL) activity after allogeneic stein cell transplantation. The authors describe the detection of HA-I-specific T cells by peptide-loaded dimers and flow cytometry in the peripheral blood of a patient in complete remission but without GvHD after donor lymphocyte infusion for chemotherapy-resistant Philadelphia chromosome-positive acute lymphoblastic leukemia. The HA-I-specific T cells were sorted and an alloreactive, polyclonal T-cell line with specific lytic activity against HA-1-positive target cells, including leukemic cells, was established. Although P 190 bcr/abl peptide-specific CD8-positive T cells were detected in the peripheral blood at the same time, these T cells could not be expanded. Furthermore, no P 190 bcr/abl peptide-specific T-cell response could be induced in vitro, even when peptide-loaded dendritic cells were used as stimulator cells. The authors conclude that in the absence of GvHD, HA-1-specific rather than P190 bcr/abi-specific T cells are responsible for ongoing GvL activity.
引用
收藏
页码:156 / 160
页数:5
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