New generation dendritic cell vaccine for immunotherapy of acute myeloid leukemia

被引:41
作者
Subklewe, Marion [1 ]
Geiger, Christiane [2 ,3 ]
Lichtenegger, Felix S. [1 ]
Javorovic, Miran [2 ]
Kvalheim, Gunnar [4 ]
Schendel, Dolores J. [2 ,3 ]
Bigalke, Iris [2 ,4 ]
机构
[1] Klinikum Univ Munchen, Dept Internal Med 3, Munich, Germany
[2] Helmholtz Zentrum Munchen, Inst Mol Immunol, Munich, Germany
[3] Trianta Immunotherapies GmbH, D-82152 Planegg Martinsried, Germany
[4] Oslo Univ Hosp, Dept Cellular Therapy, Oslo, Norway
关键词
AML; Cancer immunotherapy; Clinical trial; Dendritic cells; Vaccine; PIVAC; 13; MINIMAL RESIDUAL DISEASE; WT1 PEPTIDE VACCINATION; COMPLETE REMISSION; CANCER-IMMUNOTHERAPY; PROGNOSTIC IMPACT; GENE-EXPRESSION; FLOW-CYTOMETRY; T-LYMPHOCYTES; TUMOR LYSATE; RESPONSES;
D O I
10.1007/s00262-014-1600-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Dendritic cell (DC)-based immunotherapy is a promising strategy for the elimination of minimal residual disease in patients with acute myeloid leukemia (AML). Particularly, patients with a high risk of relapse who are not eligible for hematopoietic stem cell transplantation could benefit from such a therapeutic approach. Here, we review our extensive studies on the development of a protocol for the generation of DCs with improved immunogenicity and optimized for the use in cell-based immunotherapy. This new generation DC vaccine combines the production of DCs in only 3 days with Toll-like receptor-signaling-induced cell maturation. These mature DCs are then loaded with RNA encoding the leukemia-associated antigens Wilm's tumor protein 1 and preferentially expressed antigen in melanoma in order to stimulate an AML-specific T-cell-based immune response. In vitro as well as in vivo studies demonstrated the enhanced capacity of these improved DCs for the induction of tumor-specific immune responses. Finally, a proof-of-concept Phase I/II clinical trial is discussed for post-remission AML patients with high risk for disease relapse.
引用
收藏
页码:1093 / 1103
页数:11
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