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精准癌症免疫疗法:优化基于树突状细胞的策略以诱导针对个体患者肿瘤的肿瘤抗原特异性T细胞应答。

Precision cancer immunotherapy: optimizing dendritic cell-based strategies to induce tumor antigen-specific T-cell responses against individual patient tumors.

作者信息

Osada Takuya, Nagaoka Koji, Takahara Masashi, Yang Xiao Yi, Liu Cong-Xiao, Guo Hongtao, Roy Choudhury Kingshuk, Hobeika Amy, Hartman Zachary, Morse Michael A, Lyerly H Kim

机构信息

Departments of *Surgery §Medicine, Duke University Medical Center ‡Department of Biostatistics & Bioinformatics, Duke University, Durham, NC †Medinet Medical Institute, MEDINET Co., Ltd, Tokyo, Japan.

出版信息

J Immunother. 2015 May;38(4):155-64. doi: 10.1097/CJI.0000000000000075.

Abstract

Most dendritic cell (DC)-based vaccines have loaded the DC with defined antigens, but loading with autologos tumor-derived antigens would generate DCs that activate personalized tumor-specific T-cell responses. We hypothesized that DC matured with an optimized combination of reagents and loaded with tumor-derived antigens using a clinically feasible electroporation strategy would induce potent antitumor immunity. We first studied the effects on DC maturation and antigen presentation of the addition of picibanil (OK432) to a combination of zoledronic acid, tumor necrosis factor-α, and prostaglandin E2. Using DC matured with the optimized combination, we tested 2 clinically feasible sources of autologous antigen for electroloading, total tumor mRNA or total tumor lysate, to determine which stimulated more potent antigen-specific T cells in vitro and activated more potent antitumor immunity in vivo. The combination of tumor necrosis factor-α/prostaglandin E2/zoledronic acid/OK432 generated DC with high expression of maturation markers and antigen-specific T-cell stimulatory function in vitro. Mature DC electroloaded with tumor-derived mRNA [mRNA electroporated dendritic cell (EPDC)] induced greater expansion of antigen-specific T cells in vitro than DC electroloaded with tumor lysate (lysate EPDC). In a therapeutic model of MC38-carcinoembryonic antigen colon cancer-bearing mice, vaccination with mRNA EPDC induced the most efficient anti-carcinoembryonic antigen cellular immune response, which significantly suppressed tumor growth. In conclusion, mature DC electroloaded with tumor-derived mRNA are a potent cancer vaccine, especially useful when specific tumor antigens for vaccination have not been identified, allowing autologous tumor, and if unavailable, allogeneic cell lines to be used as an unbiased source of antigen. Our data support clinical testing of this strategy.

摘要

大多数基于树突状细胞(DC)的疫苗都用特定抗原负载DC,但用自体肿瘤衍生抗原负载会产生能激活个性化肿瘤特异性T细胞反应的DC。我们推测,用试剂的优化组合使DC成熟,并使用临床可行的电穿孔策略用肿瘤衍生抗原负载DC,将诱导强大的抗肿瘤免疫。我们首先研究了将溶链菌制剂(OK432)添加到唑来膦酸、肿瘤坏死因子-α和前列腺素E2的组合中对DC成熟和抗原呈递的影响。使用用优化组合成熟的DC,我们测试了两种临床可行的自体抗原电负载来源,即总肿瘤mRNA或总肿瘤裂解物,以确定哪种在体外刺激更强的抗原特异性T细胞,以及在体内激活更强的抗肿瘤免疫。肿瘤坏死因子-α/前列腺素E2/唑来膦酸/OK432的组合在体外产生了具有高成熟标志物表达和抗原特异性T细胞刺激功能的DC。用肿瘤衍生mRNA电负载的成熟DC[mRNA电穿孔树突状细胞(EPDC)]在体外比用肿瘤裂解物电负载的DC(裂解物EPDC)诱导更强的抗原特异性T细胞扩增。在携带MC38-癌胚抗原结肠癌的小鼠治疗模型中,用mRNA EPDC接种诱导了最有效的抗癌胚抗原细胞免疫反应,显著抑制了肿瘤生长。总之,用肿瘤衍生mRNA电负载的成熟DC是一种有效的癌症疫苗,当尚未确定用于接种的特异性肿瘤抗原时特别有用,允许使用自体肿瘤,如果没有自体肿瘤,则使用同种异体细胞系作为无偏倚的抗原来源。我们的数据支持对该策略进行临床试验。

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