Department of Pathology and Lab Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Department of Pathology and Lab Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA; Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Biochem Biophys Res Commun. 2023 Nov 5;680:51-60. doi: 10.1016/j.bbrc.2023.09.018. Epub 2023 Sep 12.
Adoptive immunotherapy using chimeric antigen receptor (CAR) T cells has made significant success in treating hematological malignancies, paving the way for solid tumors like prostate cancer. However, progress is impeded by a paucity of suitable target antigens. A novel carbohydrate antigen, F77, is expressed on both androgen-dependent and androgen-independent prostate cancer cells, making it a potential immunotherapy target. This study entails the generation and evaluation of a second-generation CAR against a carbohydrate antigen on malignant prostate cancer cells. Using a single chain fragment variable (scFv) from an F77-specific mouse monoclonal antibody, we created second-generation CARs with CD28 and CD137 (4-1BB) costimulatory signals. F77 expressing lentiviral CAR T cells produce cytokines and kill tumor cells in a F77 expression-dependent manner. These F77-specific CAR T cells eradicate prostate tumors in a human xenograft model employing PC3 cells. These findings validate F77 as a promising immunotherapeutic target for prostate cancer and other malignancies with this aberrant carbohydrate structure.
嵌合抗原受体 (CAR) T 细胞的过继免疫疗法在治疗血液恶性肿瘤方面取得了显著的成功,为前列腺癌等实体肿瘤的治疗开辟了道路。然而,由于合适的靶抗原有限,该疗法的发展受到了阻碍。一种新型的碳水化合物抗原 F77 在上皮来源的前列腺癌细胞上均有表达,包括雄激素依赖性和雄激素非依赖性前列腺癌细胞,使其成为一种潜在的免疫治疗靶标。本研究旨在生成并评估针对恶性前列腺癌细胞上的碳水化合物抗原的第二代 CAR。我们使用 F77 特异性小鼠单克隆抗体的单链片段可变区(scFv),构建了具有 CD28 和 CD137(4-1BB)共刺激信号的第二代 CAR。表达 F77 的慢病毒 CAR T 细胞能够产生细胞因子,并以 F77 表达依赖性的方式杀伤肿瘤细胞。这些 F77 特异性 CAR T 细胞能够在用人前列腺癌细胞系 PC3 建立的异种移植模型中根除前列腺肿瘤。这些发现验证了 F77 作为前列腺癌和其他具有这种异常碳水化合物结构的恶性肿瘤的一种很有前途的免疫治疗靶标。