Vaccination of multiple myeloma patients with idiotype-pulsed dendritic cells: immunological and clinical aspects

被引:172
作者
Titzer, S
Christensen, O
Manzke, O
Tesch, H
Wolf, J
Emmerich, B
Carsten, C
Diehl, V
Bohlen, H
机构
[1] Univ Cologne, Dept Internal Med 1, D-50924 Cologne, Germany
[2] Univ Munich, Dept Med, D-80336 Munich, Germany
[3] Univ Bonn, Inst Zool, D-5300 Bonn, Germany
关键词
dendritic cells; CD34(+) progenitor cells; vaccination; idiotype; multiple myeloma;
D O I
10.1046/j.1365-2141.2000.01958.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiple myeloma (MM) is characterized by a clonal proliferation of malignant plasma cells in the bone marrow secreting a monoclonal immunoglobulin (paraprotein) with specific antigenic determinants, the idiotype (Id), which can be regarded. as a tumour-associated antigen (TAA). In order to analyse the impact of a dendritic cell (DC)-based vaccine, 11 patients with advanced MM were treated with CD34 stem cell-derived dendritic cells that were pulsed with Id peptides. Subsequently, the patients received three boost immunizations every other week with a combination of Id and granulocyte-macrophage colony-stimulating factor (GM-CSF) (nine patients) or with Id peptide-pulsed dendritic cells again (two patients). The treatment was well tolerated with, no side-effects. The present clinical study was a proof of concept analysis of dendritic cell-based vaccines in MM. The capacity of the dendritic cells to activate idiotype-specific T cells was verified by in vitro stimulation experiments before the vaccination therapy. Immunological effects of the Id vaccination were analysed by monitoring changes in anti-idiotype antibody titres and idiotype-specific T-cell activity. After vaccination, three out of 10 analysed patients showed increased anti-idiotype antibody serum titres, indicating the induction of an idiotype-specific humoral immune response. The idiotype-specific T-cell response analysed by ELISpot was increased in four out of 10 analysed patients after vaccination, and one patient: had a decreased plasma cell infiltration in the bone marrow. In conclusion, five out of 11 patients showed a biological response after vaccination. Thus, our data indicate that immunotherapy with Id-pulsed DCs in MM patient's is feasible and safe. DC generated from CD34(+) progenitor cells can serve as a natural adjuvant for the induction of clinically relevant humoral and cellular idiotype-specific immune responses in patients suffering from advanced MM.
引用
收藏
页码:805 / 816
页数:12
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