Tao M H, Levy R
Department of Medicine, School of Medicine, Stanford University, California 94305.
Nature. 1993 Apr 22;362(6422):755-8. doi: 10.1038/362755a0.
To produce a vaccine against cancer, antigens must be found that are preferentially expressed by tumour cells and can induce an immune response against the tumour. The variable regions of the immunoglobulin molecules expressed on malignant B cells (idiotypes) are tumour-specific, but are weak immunogens. To induce an immune response in animals or humans, the idiotypic protein has therefore to be chemically coupled to a strongly immunogenic protein and mixed with an adjuvant. The resulting response can protect animals from subsequent tumour challenge, and cure animals with established tumours in combination with chemotherapy. Granulocyte-macrophage colony-stimulating factor (GM-CSF) augments antigen presentation in a variety of cells. Here we show that by fusing a tumour-derived idiotype to GM-CSF, it can be converted into a strong immunogen capable of inducing idiotype-specific antibodies without other carrier proteins or adjuvants and of protecting recipient animals from challenge with an otherwise lethal dose of tumour cells. This approach may be applicable to the design of vaccines for a variety of other diseases.
要生产抗癌疫苗,必须找到优先由肿瘤细胞表达且能诱导针对肿瘤的免疫反应的抗原。恶性B细胞上表达的免疫球蛋白分子的可变区(独特型)是肿瘤特异性的,但免疫原性较弱。因此,为了在动物或人类中诱导免疫反应,必须将独特型蛋白化学偶联到强免疫原性蛋白上,并与佐剂混合。产生的反应可以保护动物免受后续肿瘤攻击,并与化疗联合治愈患有已形成肿瘤的动物。粒细胞-巨噬细胞集落刺激因子(GM-CSF)可增强多种细胞中的抗原呈递。我们在此表明,通过将肿瘤衍生的独特型与GM-CSF融合,它可以转化为一种强免疫原,能够在没有其他载体蛋白或佐剂的情况下诱导独特型特异性抗体,并保护受体动物免受否则会致死剂量的肿瘤细胞攻击。这种方法可能适用于多种其他疾病疫苗的设计。