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表达针对经常表达的甲状腺髓样癌抗原降钙素、CEA 和 RET M918T 的免疫受体的 T 细胞。

T Cells Engineered to Express Immunoreceptors Targeting the Frequently Expressed Medullary Thyroid Cancer Antigens Calcitonin, CEA, and RET M918T.

机构信息

Earle A. Chiles Research Institute, Providence Cancer Institute, Portland, Oregon, USA.

出版信息

Thyroid. 2022 Jul;32(7):789-798. doi: 10.1089/thy.2022.0020.

Abstract

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.

摘要

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。

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