Daniels Gregory A, Sanchez-Perez Luis, Diaz Rosa Maria, Kottke Timothy, Thompson Jill, Lai Maoyi, Gough Michael, Karim Mahzuz, Bushell Andrew, Chong Heung, Melcher Alan, Harrington Kevin, Vile Richard G
Molecular Medicine Program, Mayo Clinic, Rochester, Minnesota 55905, USA.
Nat Biotechnol. 2004 Sep;22(9):1125-32. doi: 10.1038/nbt1007. Epub 2004 Aug 1.
We describe a simple technology used to cure an established metastatic disease. Intradermal injection of plasmid DNA encoding a transcriptionally targeted cytotoxic gene, along with hsp70, not only promoted tissue-specific, inflammatory killing of normal melanocytes, but also induced a CD8(+) T-cell-dependent, antigen-specific response in mice that eradicated systemically established B16 tumors. This CD8(+) T cell response was subsequently suppressed in vivo within a few days. The data demonstrate that deliberate destruction of normal tissue can be exploited to generate immunity against a malignant disease originating from that tissue. This approach obviates the need to identify tumor antigens and does not require complex isolation of tumor cells or their derivatives. In addition, it provides a model system for studying the mechanisms underlying the etiology and control of autoimmune diseases. Finally, despite targeting normal tissue, therapy could be separated from development of overt autoimmune symptoms, suggesting that the strategy may be valuable against tumors derived from both non-essential and essential tissue types.
我们描述了一种用于治愈已形成的转移性疾病的简单技术。皮内注射编码转录靶向细胞毒性基因的质粒DNA以及热休克蛋白70(hsp70),不仅促进了正常黑素细胞的组织特异性炎症杀伤,还在小鼠体内诱导了一种依赖CD8(+) T细胞的抗原特异性反应,从而根除了全身形成的B16肿瘤。这种CD8(+) T细胞反应随后在几天内被体内抑制。数据表明,对正常组织的蓄意破坏可被利用来产生针对源自该组织的恶性疾病的免疫力。这种方法无需识别肿瘤抗原,也不需要复杂地分离肿瘤细胞或其衍生物。此外,它为研究自身免疫性疾病的病因和控制机制提供了一个模型系统。最后,尽管靶向正常组织,但治疗可与明显的自身免疫症状的发展相分离,这表明该策略可能对源自非必需和必需组织类型的肿瘤都有价值。