利用dna疫苗治疗脑肿瘤

T. Lichtor
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引用次数: 0

摘要

癌症患者正常细胞和恶性细胞之间的抗原差异构成了临床免疫治疗策略的基本原理。由于肿瘤细胞的抗原表型在同一恶性细胞群中的不同细胞之间差异很大,因此用疫苗免疫,刺激对癌细胞表达的广泛肿瘤抗原的免疫,可能比用单一抗原的疫苗免疫更有效。通过将DNA从肿瘤转移到高免疫原性细胞系中制备的疫苗可以包含具有患者肿瘤特征的肿瘤抗原阵列。低免疫原性肿瘤抗原是恶性细胞的特征,如果它们被高免疫原性细胞表达,可以变成强抗原。通过将C3H/He小鼠中自发产生的乳腺癌的基因组DNA转移到具有高度免疫原性的小鼠成纤维细胞系中,在那里表达指定肿瘤抗原的基因,制备了一种基于DNA的疫苗。在dna转移之前对成纤维细胞进行修饰,使其分泌一种免疫增强细胞因子并表达同种异体MHC i类决定因子。在乳腺癌转移到大脑的动物模型中,通过两项独立的体外试验,将疫苗直接引入肿瘤床刺激了全身细胞抗肿瘤免疫反应,并延长了荷瘤小鼠的寿命。此外,使用针对各种t细胞亚群的抗体,确定了全身细胞抗肿瘤免疫是由CD8 +, CD4 +和NK/LAK细胞介导的。此外,还开发了一种富集策略,以增加疫苗中免疫治疗细胞的比例,从而增强抗肿瘤免疫能力。最后,在脑内注射富集疫苗的荷瘤小鼠脾细胞中发现调节性T细胞(CD4 + CD25 + foxp3 +阳性)相对缺乏。目前正在探索以dna为基础的基因组疫苗在治疗多种脑肿瘤中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment of Brain Tumors Using DNA-Based Vaccines
Antigenic differences between normal and malignant cells of the cancer patient form the rationale for clinical immunotherapeutic strategies. Because the antigenic phenotype of neoplastic cells varies widely among different cells within the same malignant cell-population, immunization with a vaccine that stimulates immunity to the broad array of tumor antigens expressed by the cancer cells is likely to be more efficacious than immunization with a vaccine for a single antigen. A vaccine prepared by transfer of DNA from the tumor into a highly immunogenic cell line can encompass the array of tumor antigens that characterize the patient's neoplasm. Poorly immunogenic tumor antigens, characteristic of malignant cells, can become strongly antigenic if they are expressed by highly immunogenic cells. A DNA-based vaccine was prepared by transfer of genomic DNA from a breast cancer that arose spontaneously in a C3H/He mouse into a highly immunogenic mouse fibroblast cell line, where genes specifying tumor-antigens were expressed. The fibroblasts were modified in advance of DNA-transfer to secrete an immune augmenting cytokine and to express allogeneic MHC class I-determinants. In an animal model of breast cancer metastatic to the brain, introduction of the vaccine directly into the tumor bed stimulated a systemic cellular anti-tumor immune response measured by two independent in vitro assays and prolonged the lives of the tumor-bearing mice. Furthermore, using antibodies against the various T-cell subsets, it was de- termined that the systemic cellular anti-tumor immunity was mediated by CD8 + , CD4 + and NK/LAK cells. In addition an enrichment strategy has also been developed to increase the proportion of immunotherapeutic cells in the vaccine which has resulted in the development of enhanced anti-tumor immunity. Finally regulatory T cells (CD4 + CD25 + Fox p3 + -positive) were found to be relatively deficient in the spleen cells from the tumor-bearing mice injected intracerebrally with the enriched vaccine. The application of DNA-based genomic vaccines for the treatment of a variety of brain tumors is being explored.
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