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Allogeneic Dendritic Cells Fused with Tumor Cells: Preclinical Results and Outcome of a Clinical Phase I/II Trial in Patients with Metastatic Renal Cell Carcinoma

医学 肾细胞癌 外周血单个核细胞 免疫疗法 树突状细胞 进行性疾病 免疫系统 抗原 黑色素瘤 临床试验 内科学 肿瘤科 免疫学 癌症研究 疾病 体外 生物 生物化学
作者
Angela Märten,Sabine Renoth,Thomas Heinicke,Peter Albers,Andreas Pauli,Ulrich Mey,Reiner Caspari,Dimitri Flieger,Peter Hanfland,Alexander von Ruecker,Anna Maria Eis‐Hübinger,Stefan C. Müller,Ingo Schwaner,Uwe Lohmann,Guido Heylmann,Tilman Sauerbruch,Ingo G.H. Schmidt‐Wolf
出处
期刊:Human Gene Therapy [Mary Ann Liebert]
卷期号:14 (5): 483-494 被引量:146
标识
DOI:10.1089/104303403321467243
摘要

Therapeutic vaccination with dendritic cells (DC) can lead to tumor regression in animal models and has shown promising results in the first clinical trials of metastatic renal cell carcinoma and malignant melanoma. In vitro data and results of a clinical phase I/II trial using DC tumor fusions in patients with progressive metastatic renal cell carcinoma are presented here. In addition to toxicity and feasibility, complex immune monitoring was a point of interest. DC precursor cells were obtained from the peripheral blood mononuclear cells (PBMCs) of healthy donors and were fused with either allogeneic (8 patients) or autologous (4 patients) renal tumor cells. In total, 12 patients with progressive metastatic renal cell carcinoma were treated with an average of 2.8 × 107 tumor cells fused with 1.8 × 107 DC each administered on days 0, 28, and 56 intradermally. Fusion efficacy for the tumor cells used was 14.3% ± 7.8%. Cell viability was 59.8% ± 6.8% after fusion and irradiation. We observed no adverse effects and no difference in clinical outcome between the allogeneic and the autologous treatment. Eight patients remained in a progressive disease state and four patients in a stable disease state. T-cell immunity was carefully monitored before, during, and after treatment. Delayed-type hypersensitivity (DTH) reaction using tumor cells was positive after treatment in 7 of 12 patients, 2 of whom were found to have stable disease. An increase in the reactivity against recall antigens was seen in most patients. Interestingly, cytotoxicity of peripheral blood lymphocytes (PBLs) against renal cell carcinoma cells increased during treatment as well as the percentage of interferon-γ-secreting cells. This effect was significantly enhanced within the group that had stable disease. The lack of adverse effects together with positive immunologic signs justifies further investigation of this novel therapeutic approach. Further studies are necessary to test for clinical effectiveness in patients with tumors, especially those with less advanced disease.
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