Herrero Mj, R Botella, R Algás, Marco Fm, Aliño Sf
Gene Therapy Group, Dpto. Farmacologia, Fac. Medicina, Univ. Valencia, Valencia, España.
Clin Med Oncol. 2008;2:257-65. doi: 10.4137/cmo.s586. Epub 2008 Mar 25.
Cancer vaccines have always been in the scope of gene therapy research. One of the most successful approaches has been working with genetically modified tumor cells. However, to become a clinical reality, tumor cells must suffer a long and risky process from the extraction from the patient to the reimplantation as a vaccine. In this work, we explain our group's approach to reduce the cell number required to achieve an immune response against a melanoma murine model, employing bead-selected B16 tumor cells expressing GM-CSF and B7.2.
癌症疫苗一直处于基因治疗研究的范畴内。最成功的方法之一是使用基因改造的肿瘤细胞。然而,要成为临床现实,肿瘤细胞从患者体内提取到作为疫苗重新植入的过程必须经历漫长且有风险的过程。在这项工作中,我们阐述了我们团队的方法,即采用表达GM-CSF和B7.2的磁珠分选B16肿瘤细胞,以减少实现针对黑色素瘤小鼠模型的免疫反应所需的细胞数量。