Center for Antibody Therapeutics, Division of Infectious Diseases, Department of Medicine, University of Pittsburgh Medical School, Pittsburgh, PA, United States.
Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Front Immunol. 2023 Jan 25;14:1070492. doi: 10.3389/fimmu.2023.1070492. eCollection 2023.
Ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) is a type II transmembrane glycoprotein expressed in many tissues. High expression levels of ENPP1 have been observed in many cancer types such as lung cancer, ovarian cancer, and breast cancer. Such overexpression has been associated with poor prognosis in these diseases. Hence, ENPP1 is a potential target for immunotherapy across multiple cancers. Here, we isolated and characterized two high-affinity and specific anti-ENPP1 Fab antibody candidates, 17 and 3G12, from large phage-displayed human Fab libraries. After conversion to IgG1, the binding of both antibodies increased significantly due to avidity effects. Based on these antibodies, we generated antibody-drug conjugates (ADCs), IgG-based bispecific T-cell engagers (IbTEs), and CAR T-cells which all exhibited potent killing of ENPP1-expressing cells. Thus, these various antibody-derived modalities are promising therapeutic candidates for cancers expressing human ENPP1.
核苷酸焦磷酸酶/磷酸二酯酶 1(ENPP1)是一种在许多组织中表达的 II 型跨膜糖蛋白。在许多癌症类型中,如肺癌、卵巢癌和乳腺癌,都观察到 ENPP1 的高表达水平。这种过表达与这些疾病的不良预后相关。因此,ENPP1 是多种癌症免疫治疗的潜在靶点。在这里,我们从大型噬菌体展示的人源 Fab 文库中分离和鉴定了两种高亲和力和特异性的抗 ENPP1 Fab 抗体候选物 17 和 3G12。转化为 IgG1 后,由于亲和力效应,两种抗体的结合显著增加。基于这些抗体,我们生成了抗体药物偶联物(ADC)、基于 IgG 的双特异性 T 细胞衔接器(IbTE)和 CAR T 细胞,它们都表现出对表达 ENPP1 的细胞的有效杀伤。因此,这些各种抗体衍生的方式是表达人源 ENPP1 的癌症的有前途的治疗候选物。