Institute of Biological Chemistry, Faculty of Chemistry, University of Vienna, 1090, Vienna, Austria.
Syntab Therapeutics GmbH, 52074, Aachen, Germany.
Sci Rep. 2017 Dec 14;7(1):17592. doi: 10.1038/s41598-017-17627-0.
Immuno-oncology approaches mainly utilize monoclonal antibodies or protein-based scaffolds that bind with high affinity to cancer cells and can generate an immune response. Peptides can also bind with high affinity to cancer cells and are intermediate in size between antibodies and small molecules. They are also synthetically accessible and therefore easily modified to optimize their stability, binding affinity and selectivity. Here we describe the design of immune system engagers (ISErs), a novel class of synthetic peptide-based compounds that bind specifically to cancer cells and stimulate the immune system. A prototype, Y9, targets integrin α, which is overexpressed on several cancer cells, and activates the immune system via a formyl methionine-containing effector peptide. Injection of Y9 leads to immune cell infiltration into tissue and prevents tumor formation in a guinea pig model. The anti-tumor activity and synthetic accessibility of Y9 illustrate that ISErs could be applied to a wide variety of targets and diseases.
免疫肿瘤学方法主要利用单克隆抗体或蛋白质支架,这些支架与癌细胞具有高亲和力,可以引发免疫反应。肽也可以与癌细胞高亲和力结合,并且在大小上介于抗体和小分子之间。它们也具有合成可及性,因此很容易进行修饰以优化其稳定性、结合亲和力和选择性。在这里,我们描述了免疫系统衔接物(ISErs)的设计,这是一类新型的合成肽基化合物,它们特异性地与癌细胞结合并刺激免疫系统。原型 Y9 靶向整合素 α,该蛋白在几种癌细胞上过度表达,并通过含有甲硫氨酸的效应肽激活免疫系统。Y9 的注射导致免疫细胞浸润到组织中,并防止豚鼠模型中的肿瘤形成。Y9 的抗肿瘤活性和合成可及性表明,ISErs 可应用于广泛的靶标和疾病。