Heather K. Lin, Dejah A. Blake, Tongrui Liu, Ruby Freeman, Gregory B. Lesinski, Lily Yang, Sarwish Rafiq
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引用次数: 0
Abstract
Pancreatic cancer is an aggressive malignancy with a 5-year survival rate of 13% that remains refractory to current immunotherapies, such as chimeric antigen receptor (CAR) T cells. These engineered cells can produce robust anti-tumor responses but require a reliable tumor-associated antigen (TAA) target. Here, we describe the retained ectodomain of Muc16, Muc16CD, as a novel TAA for targeting by CAR T cell therapy in pancreatic cancer. We establish clinically relevant, endogenous Muc16 and Muc16CD expression in pancreatic tumor tissues for CAR T cell targeting. Muc16CD-directed CAR T cells can both recognize and activate in a polyfunctional manner in response to patient-derived pancreatic tumor cells. Last, we demonstrate that Muc16CD-directed CAR T cells can elicit an anti-tumor response with significantly enhanced tumor control and survival benefits in a pancreatic tumor model. Overall, these findings demonstrate the utility of Muc16CD-targeted CAR T cell therapy in the novel setting of pancreatic cancer.
胰腺癌是一种侵袭性恶性肿瘤,5 年生存率仅为 13%,对目前的免疫疗法(如嵌合抗原受体(CAR)T 细胞)仍有耐药性。这些改造细胞能产生强大的抗肿瘤反应,但需要可靠的肿瘤相关抗原(TAA)靶点。在这里,我们描述了 Muc16 的保留外结构域 Muc16CD,它是 CAR T 细胞疗法在胰腺癌中靶向的新型 TAA。我们在胰腺肿瘤组织中建立了与临床相关的内源性 Muc16 和 Muc16CD 表达,用于 CAR T 细胞靶向治疗。以 Muc16CD 为靶向的 CAR T 细胞既能识别患者来源的胰腺肿瘤细胞,又能以多功能方式激活这些细胞。最后,我们证明了 Muc16CD 引导的 CAR T 细胞能在胰腺肿瘤模型中引起抗肿瘤反应,显著提高肿瘤控制率和生存率。总之,这些研究结果证明了 Muc16CD 靶向 CAR T 细胞疗法在胰腺癌这种新型疾病中的实用性。