研究概要
复发转移性神经母细胞瘤 (NB) 的儿童患者 5 年生存率极低。
中文摘要
复发性转移性神经母细胞瘤(NB)儿童患者的5年生存率极低,亟需新型治疗方法。黑色素瘤细胞黏附分子(MCAM/CD146/MUC18)表达于多种儿童实体瘤(包括NB),是一个新型免疫治疗靶点。本研究将CAR mRNA通过非病毒电转导入体外扩增的NK细胞,制备靶向MCAM的嵌合抗原受体(CAR)NK细胞。与模拟处理NK细胞相比,抗MCAM CAR表达显著增强NK细胞对MCAM高表达NB细胞的细胞毒活性,但对MCAM低表达或敲除NB细胞无此作用。抗MCAM-CAR-NK细胞治疗显著降低NB异种移植小鼠模型中的肿瘤生长,并延长动物生存期。NKTR-255是一种聚合物偶联的重组人白细胞介素15激动剂,可显著刺激NK细胞增殖和扩增,并进一步增强抗MCAM-CAR-NK细胞在体外的细胞毒活性及其体内抗NB肿瘤疗效。我们的临床前研究表明,体外扩增和改造的抗MCAM-CAR-NK细胞单独使用和/或与NKTR-255联合使用,是靶向MCAM高表达恶性NB的有前景新型替代治疗方法。
展开英文摘要原文
Pediatric patients with recurrent metastatic neuroblastoma (NB) have a dismal 5-year survival. Novel therapeutic approaches are urgently needed. The melanoma cell adhesion molecule (MCAM/CD146/MUC18) is expressed in a variety of pediatric solid tumors, including NB, and constitutes a novel target for immunotherapy. Here, we developed a chimeric antigen receptor (CAR) expressing natural killer (NK) cell-targeting MCAM by non-viral electroporation of CAR mRNA into ex vivo expanded NK cells. Expression of anti-MCAM CAR significantly enhanced NK cell cytotoxic activity compared to mock NK cells against MCAM high but not MCAM low/knockout NB cells in vitro . Anti-MCAM-CAR-NK cell treatment significantly decreased tumor growth and prolonged animal survival in an NB xenograft mouse model. NKTR-255, a polymer-conjugated recombinant human interleukin-15 agonist, significantly stimulated NK cell proliferation and expansion and further enhanced the in vitro cytotoxic activity and in vivo anti-tumor efficacy of anti-MCAM-CAR-NK cells against NB. Our preclinical studies demonstrate that ex vivo expanded and modified anti-MCAM-CAR-NK cells alone and/or in combination with NKTR-255 are promising novel alternative therapeutic approaches to targeting MCAM high malignant NB.
论文信息
- 作者
- Luo W、Gardenswartz A、Hoang H、Chu Y、Tian M、Liao Y、Ayello J、Rosenblum JM
- 单位
- Department of Pediatrics, New York Medical College, Valhalla, NY 10595, USA.United States
- 期刊
- Molecular therapy. Oncology2024 Dec 19