共 29 条
Evidence that specific T lymphocytes may participate in the elimination of chronic myelogenous leukemia
被引:538
作者:

Molldrem, JJ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Blood & Marrow Transplantat, Sect Transplantat Immunol, Houston, TX 77030 USA

Lee, PP
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Blood & Marrow Transplantat, Sect Transplantat Immunol, Houston, TX 77030 USA

Wang, CQ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Blood & Marrow Transplantat, Sect Transplantat Immunol, Houston, TX 77030 USA

Felio, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Blood & Marrow Transplantat, Sect Transplantat Immunol, Houston, TX 77030 USA

Kantarjian, HM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Blood & Marrow Transplantat, Sect Transplantat Immunol, Houston, TX 77030 USA

Champlin, RE
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Blood & Marrow Transplantat, Sect Transplantat Immunol, Houston, TX 77030 USA

Davis, MM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Blood & Marrow Transplantat, Sect Transplantat Immunol, Houston, TX 77030 USA
机构:
[1] Univ Texas, MD Anderson Canc Ctr, Dept Blood & Marrow Transplantat, Sect Transplantat Immunol, Houston, TX 77030 USA
[2] Stanford Univ, Dept Med, Stanford, CA 94305 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
[4] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Microbiol & Immunol, Stanford, CA 94305 USA
关键词:
D O I:
10.1038/79526
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:
Although the immune system has long been implicated in the control of cancer, evidence for specific and efficacious immune responses in human cancer has been lacking. In the case of chronic myelogenous leukemia (CML), either allogeneic bone marrow transplant (BMT) or interferon-alpha 2b (IFN alpha 2b) therapy can result in complete remission, but the mechanism for prolonged disease control is unknown and may involve immune anti-leukemic responses. We previously demonstrated that PR1, a peptide derived from proteinase 3, is a potential target for CML-specific T cells. Here we studied 38 CML patients treated with allogeneic BMT, IFN-alpha 2b or chemotherapy to look for PR1-specific T cells using PR1/HLA-A*0201 tetrameric complexes. There was a strong correlation between the presence of PR1-specific T cells and clinical responses after IFN-alpha and allogeneic BMT. This provides for the first time direct evidence of a role for T-cell immunity in clearing malignant cells.
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页码:1018 / 1023
页数:6
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