Immunogenicity and therapeutic efficacy of dendritic-tumor hybrid cells generated by electrofusion

被引:66
作者
Hayashi, T
Tanaka, H
Tanaka, J
Wang, RF
Averbook, BJ
Cohen, PA
Shu, SY
机构
[1] Cleveland Clin Fdn, Surg Res Ctr, Cleveland, OH 44195 USA
[2] Case Western Reserve Univ, MetroHlth Med Ctr, Dept Surg, Cleveland, OH 44106 USA
[3] Baylor Coll Med, Ctr Gene Therapy, Houston, TX 77030 USA
关键词
dendritic cells; electrofusion; T cells; tumor immunity; vaccination; immunotherapy;
D O I
10.1006/clim.2002.5224
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) are potent antigen-presenting cells capable of inducing strong immune responses to weak tumor-associated antigens. Among various DC-based approaches, cancer immunotherapy with DC-tumor fusion hybrids offers advantages of polyclonal stimulation of a diverse array of tumor antigens. However, prevalent fusion methods using chemical fusogens such as polyethylene glycol often result in toxicity and low fusion efficiency. In this article, we describe an electrofusion technique, applicable to processing large numbers of cells with consistent and high fusion efficiency. Generation of fusion hybrids was verified by unequivocal experimental evidence. In animal models, fusion hybrids expressed the mature DC-like phenotype. They stimulated both CD4 and CD8 tumor-specific T cells to secrete interferon-gamma in vitro. In immunotherapy, a single vaccination with DC-tumor fusion cells along with interleukin-12 as an adjuvant eradicated tumors established in the skin nd lung. These results provide an impetus for treating cancer patients with similarly generated cells. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:14 / 20
页数:7
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