Met Ozcan, Svane Inge Marie
Department of Hematology, Center for Cancer Immune Therapy (CCIT), University Hospital Herlev, Copenhagen, Denmark.
Methods Mol Biol. 2013;969:275-92. doi: 10.1007/978-1-62703-260-5_17.
The observation that dendritic cells (DCs) charged with tumor-associated antigens (TAAs) is a potent strategy to elicit protective immunity in tumor-bearings hosts has prompted extensive testing of DCs as cellular adjuvant in cancer vaccines. To improve the clinical development of DC-based cancer vaccines, it may be beneficial to analyze preexistent immunity against TAAs in cancer patients because it may be easier to expand a memory pool of T cells compared to generating new immunity. Recent research shows that engineering DCs to synthesize tumor epitopes endogenously by transfecting DCs with mRNA-encoding TAAs are particular effective in stimulating robust T-responses in vitro and in vivo. In this chapter, we describe the methodology to analyze for survivin-specific T cells in breast cancer patients using human DCs engineered with survivin mRNA.
携带肿瘤相关抗原(TAA)的树突状细胞(DC)可在荷瘤宿主中引发保护性免疫,这一观察结果促使人们广泛测试DC作为癌症疫苗中的细胞佐剂。为了改善基于DC的癌症疫苗的临床开发,分析癌症患者对TAA的预先存在的免疫可能是有益的,因为与产生新的免疫相比,扩大T细胞的记忆库可能更容易。最近的研究表明,通过用编码TAA的mRNA转染DC来工程化DC以在内源合成肿瘤表位,在体外和体内刺激强大的T细胞反应方面特别有效。在本章中,我们描述了使用用生存素mRNA工程化的人DC分析乳腺癌患者中生存素特异性T细胞的方法。