King Ellen, Struck Ronja, Piskareva Olga
Cancer Bioengineering Group & Tissue Engineering Research Group (TERG), Department of Anatomy and Regenerative Medicine, RCSI University of Medicine and Health Sciences, Dublin, Ireland; School of Pharmacy and Biomolecular Sciences, RCSI University of Medicine and Health Sciences, Dublin, Ireland.
Cancer Bioengineering Group & Tissue Engineering Research Group (TERG), Department of Anatomy and Regenerative Medicine, RCSI University of Medicine and Health Sciences, Dublin, Ireland; School of Pharmacy and Biomolecular Sciences, RCSI University of Medicine and Health Sciences, Dublin, Ireland; Advanced Materials and Bioengineering Research Centre (AMBER), RCSI University of Medicine and Health Sciences and Trinity College Dublin, Dublin, Ireland.
Transl Oncol. 2025 Jan;51:102176. doi: 10.1016/j.tranon.2024.102176. Epub 2024 Nov 2.
Neuroblastoma is an embryonic tumour originating from neural crest cells and accounts for nearly 15 % of all childhood cancer deaths. Despite the implementation of intense multimodal therapy for neuroblastoma, half of the high-risk cohort will relapse with metastatic foci resistant to conventional therapies. There is an urgent need for novel precision medicine approaches to improve patient survival and ensure healthy post-treatment lives for these children. Immunotherapy holds promise for such therapeutics; however, developing effective options has been disappointing despite decades of research. The immunosuppressive tumour-immune microenvironment presents a significant challenge amplified with low mutational burden in neuroblastoma, even with the new discovered tumour antigens. Innovative, practical, and comprehensive approaches are crucial for designing and testing immunotherapies capable of passing clinical trials. Replacing animal models with physiologically relevant in vitro systems will expedite this process and provide new insights into exploitable tumour-immune cell interactions. This review examines this three-pronged approach in neuroblastoma immunotherapy: tumour antigen discovery, immunomodulation, and 3D in vitro tumour models, and discusses current and emerging insights into these strategies to address neuroblastoma immunotherapy challenges.
神经母细胞瘤是一种起源于神经嵴细胞的胚胎性肿瘤,占儿童癌症死亡总数的近15%。尽管对神经母细胞瘤实施了强化多模态治疗,但高危患者群体中有一半会复发,出现对传统疗法耐药的转移病灶。迫切需要新的精准医学方法来提高患者生存率,并确保这些儿童在治疗后能过上健康的生活。免疫疗法有望成为此类治疗手段;然而,尽管经过数十年研究,开发有效的免疫疗法仍令人失望。免疫抑制性肿瘤免疫微环境是一个重大挑战,在神经母细胞瘤中,即使有新发现的肿瘤抗原,其低突变负荷也会加剧这一挑战。创新、实用且全面的方法对于设计和测试能够通过临床试验的免疫疗法至关重要。用生理相关的体外系统取代动物模型将加快这一进程,并为可利用的肿瘤免疫细胞相互作用提供新见解。本综述探讨了神经母细胞瘤免疫疗法中的这一三方方法:肿瘤抗原发现、免疫调节和3D体外肿瘤模型,并讨论了当前和新出现的对这些策略的见解,以应对神经母细胞瘤免疫疗法的挑战。