Earle A. Chiles Research Institute, Providence Cancer Institute, Portland, Oregon, USA.
Thyroid. 2022 Jul;32(7):789-798. doi: 10.1089/thy.2022.0020.
Medullary thyroid cancer (MTC) is a rare malignancy originating from the calcitonin-producing C cells of the thyroid. Despite recent therapeutic advances, metastatic MTC remains incurable. Adoptive cell therapy (ACT) using genetically engineered T cells targeting either tissue-restricted tumor-associated antigens or mutated neoantigens has led to durable remissions in other metastatic solid tumors. The majority of MTC express the tumor-associated antigens calcitonin and carcinoembryonic antigen (CEA), and ∼40% of MTC harbor the RET M918T oncogenic driver mutation. We developed and characterized three immunoreceptors that recognize extracellular CEA, a calcitonin epitope presented by HLA-A24:02, or an RET M918T neoepitope restricted by HLA-DPB104:01/02. The chimeric antigen receptor (CAR) targeting CEA was synthetically designed, while the T cell receptors (TCRs) targeting calcitonin and RET M918T were isolated from a transgenic mouse and patient with MTC, respectively. These immunoreceptors were genetically engineered into peripheral blood T cells and tested for antigen specificity and antitumor activity. T cells expressing the anti-CEA CAR or the calcitonin-reactive TCR produced effector cytokines and displayed cytotoxicity against cell lines expressing their cognate antigen . In immunodeficient mice harboring a human MTC cell line, the adoptive transfer of T cells engineered to express the anti-CEA CAR or calcitonin-reactive TCR led to complete tumor regression. T cells expressing the HLA-DPB104:01/02-restricted TCR targeting RET M918T, which was cloned from peripheral blood CD4 T cells of a patient with MTC, demonstrated specific reactivity against cells pulsed with the mutated peptide and MTC tumor cells that expressed HLA-DPB104:01 and RET M918T. The preclinical data presented herein demonstrate the potential of using genetically engineered T cells targeting CEA, calcitonin, and/or RET M918T to treat metastatic MTC.
甲状腺髓样癌(MTC)是一种罕见的恶性肿瘤,起源于甲状腺的降钙素产生 C 细胞。尽管最近有了治疗进展,但转移性 MTC 仍然无法治愈。使用针对组织受限的肿瘤相关抗原或突变的新抗原的基因工程 T 细胞进行过继细胞治疗(ACT),已导致其他转移性实体瘤的持久缓解。大多数 MTC 表达肿瘤相关抗原降钙素和癌胚抗原(CEA),并且大约 40%的 MTC 携带 RET M918T 致癌驱动突变。我们开发并鉴定了三种免疫受体,它们可以识别细胞外 CEA、由 HLA-A24:02 呈递的降钙素表位或由 HLA-DPB104:01/02 限制的 RET M918T 新抗原。针对 CEA 的嵌合抗原受体(CAR)是合成设计的,而针对降钙素和 RET M918T 的 T 细胞受体(TCR)分别从携带 MTC 的转基因小鼠和患者中分离出来。这些免疫受体被基因工程改造为外周血 T 细胞,并测试其抗原特异性和抗肿瘤活性。表达抗 CEA CAR 或降钙素反应性 TCR 的 T 细胞产生效应细胞因子,并对表达其同源抗原的细胞系显示细胞毒性。在携带人 MTC 细胞系的免疫缺陷小鼠中,过继转移工程表达抗 CEA CAR 或降钙素反应性 TCR 的 T 细胞导致完全肿瘤消退。从 MTC 患者的外周血 CD4 T 细胞中克隆的针对 HLA-DPB104:01/02 限制的 TCR 靶向 RET M918T 的 T 细胞表达,针对用突变肽和表达 HLA-DPB104:01 和 RET M918T 的 MTC 肿瘤细胞脉冲的细胞显示出特异性反应。本文提供的临床前数据表明,使用针对 CEA、降钙素和/或 RET M918T 的基因工程 T 细胞治疗转移性 MTC 具有潜力。