Haidy A. Saleh, Nicola Mitwasi, Liliana R. Loureiro, Alexandra Kegler, Karla Elizabeth González Soto, Lydia Hoffmann, Eugenia Crespo, Claudia Arndt, Ralf Bergmann, Michael Bachmann, Anja Feldmann
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引用次数: 0
摘要
在最近的研究中,我们建立了独特的适配器嵌合抗原受体(CAR)平台 RevCAR,它使用多肽表位代替抗体结构域作为细胞外 CAR 结构域。RevCAR适配器(称为RevCAR靶标模块,RevTMs)是一种双特异性抗体,可实现RevCAR系统的可逆开关,与传统CAR相比安全性更高。在这里,我们首次介绍了它在T细胞和NK-92细胞再靶向中的应用。此外,我们还介绍了针对成纤维细胞生长因子诱导的 14(Fn14)表面受体的新型 RevTM 的开发和临床前验证,该受体在胶质母细胞瘤(GBM)细胞上过度表达,因此是治疗 GBM 的一个很有前景的靶点。新型 RevTM 能有效重定向 RevCAR 修饰的 T 细胞和 NK-92 细胞,从而在体外和体内杀死 GBM 细胞。肿瘤细胞的杀伤与 IL-2、TNF-α 和/或 IFN-γ 分泌的增加有关。因此,这些研究结果让人们了解到 RevCAR T 和 NK-92 系统作为一种针对 GBM 的安全、特异性免疫治疗方法的互补潜力。
RevCAR-expressing immune effector cells for targeting of Fn14-positive glioblastoma
In recent studies, we have established the unique adapter chimeric antigen receptor (CAR) platform RevCAR which uses, as an extracellular CAR domain, a peptide epitope instead of an antibody domain. RevCAR adapters (termed RevCAR target modules, RevTMs) are bispecific antibodies that enable the reversible ON/OFF switch of the RevCAR system, improving the safety compared to conventional CARs. Here, we describe for the first time its use for retargeting of both T and NK-92 cells. In addition, we describe the development and preclinical validation of a novel RevTM for targeting of the fibroblast growth factor-inducible 14 (Fn14) surface receptor which is overexpressed on Glioblastoma (GBM) cells, and therefore serves as a promising target for the treatment of GBM. The novel RevTM efficiently redirects RevCAR modified T and NK-92 cells and leads to the killing of GBM cells both in vitro and in vivo. Tumor cell killing is associated with increased IL-2, TNF-α and/or IFN-γ secretion. Hence, these findings give an insight into the complementary potential of both RevCAR T and NK-92 systems as a safe and specific immunotherapeutic approach against GBM.
期刊介绍:
Cancer Gene Therapy is the essential gene and cellular therapy resource for cancer researchers and clinicians, keeping readers up to date with the latest developments in gene and cellular therapies for cancer. The journal publishes original laboratory and clinical research papers, case reports and review articles. Publication topics include RNAi approaches, drug resistance, hematopoietic progenitor cell gene transfer, cancer stem cells, cellular therapies, homologous recombination, ribozyme technology, antisense technology, tumor immunotherapy and tumor suppressors, translational research, cancer therapy, gene delivery systems (viral and non-viral), anti-gene therapy (antisense, siRNA & ribozymes), apoptosis; mechanisms and therapies, vaccine development, immunology and immunotherapy, DNA synthesis and repair.
Cancer Gene Therapy publishes the results of laboratory investigations, preclinical studies, and clinical trials in the field of gene transfer/gene therapy and cellular therapies as applied to cancer research. Types of articles published include original research articles; case reports; brief communications; review articles in the main fields of drug resistance/sensitivity, gene therapy, cellular therapy, tumor suppressor and anti-oncogene therapy, cytokine/tumor immunotherapy, etc.; industry perspectives; and letters to the editor.