Enrichment of functional CD8 memory T cells specific for MUC1 in bone marrow of patients with multiple myeloma

被引:94
作者
Choi, C
Witzens, M
Bucur, M
Feuerer, M
Sommerfeldt, N
Trojan, A
Ho, A
Schirrmacher, V
Goldschmidt, H
Beckhove, P
机构
[1] German Canc Res Ctr, Tumor Immunol Programme, D-69120 Heidelberg, Germany
[2] Univ Heidelberg Hosp, Dept Hematol & Oncol, Heidelberg, Germany
[3] Humboldt Univ, Med Clin, Charite, Dept Expt Rheumatol, Berlin, Germany
[4] Univ Zurich Hosp, Dept Oncol, Zurich, Switzerland
关键词
D O I
10.1182/blood-2004-01-0366
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiple myeloma (MM) is one of the most common hematologic malignancies. Despite extensive therapeutical approaches, cures remain rare exceptions. An important issue for future immunologic treatments is the characterization of appropriate tumor-associated antigens. Recently, a highly glycosylated mucin MUC1 was detected on a majority of multiple myeloma cell lines. We analyzed bone marrow and peripheral blood of 68 patients with HLA-A2-positive myeloma for the presence and functional activity of CD8 T cells specific for the MUC1-derived peptide LLLLTVLTV. Forty-four percent of the patients with MM contained elevated frequencies of MUC1-specific CD8 T cells in freshly isolated samples from peripheral blood (PB) or bone marrow (BM) compared with corresponding samples from healthy donors. BM-residing T cells possessed a higher functional capacity upon specific reactivation than PB-derived T cells with regard to interferon gamma (IFN-gamma) secretion, perforin production, and cytotoxicity. (C) 2005 by The American Society of Hematology
引用
收藏
页码:2132 / 2134
页数:3
相关论文
共 26 条
[21]  
2-G
[22]   T-cell priming in bone marrow: the potential for long-lasting protective anti-tumor immunity [J].
Schirrmacher, V ;
Feuerer, M ;
Fournier, P ;
Ahlert, T ;
Umansky, V ;
Beckhove, P .
TRENDS IN MOLECULAR MEDICINE, 2003, 9 (12) :526-534
[23]  
TAKAHASHI T, 1994, J IMMUNOL, V153, P2102
[24]  
Tricot G, 2000, HEMATOLOGY PRINCIPLE, P1398
[25]   NATURALLY PROCESSED VIRAL PEPTIDES RECOGNIZED BY CYTOTOXIC T-LYMPHOCYTES ON CELLS CHRONICALLY INFECTED BY HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 [J].
TSOMIDES, TJ ;
ALDOVINI, A ;
JOHNSON, RP ;
WALKER, BD ;
YOUNG, RA ;
EISEN, HN .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (04) :1283-1293
[26]   Idiotype-specific cytotoxic T lymphocytes in multiple myeloma: evidence for their capacity to lyse autologous primary tumor cells [J].
Wen, YJ ;
Barlogie, B ;
Yi, Q .
BLOOD, 2001, 97 (06) :1750-1755