CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
我们的工作确立了CD81作为连接放射抵抗与免疫逃逸的关键桥梁,其通过维持GBM中CD274的丰度发挥作用,并突显CD81作为优化放射免疫治疗的有前景的治疗靶点。
英文原题:Nanomedicines and cell-based therapies for embryonal tumors of the nervous system.
Nanomedicines and cell-based therapies for embryonal tumors of the nervous system.
神经系统胚胎性肿瘤是主要影响儿童人群的肿瘤。
神经系统胚胎性肿瘤主要影响儿童,其中最常见且侵袭性最强的包括神经母细胞瘤(NB)和髓母细胞瘤(MB)。NB 是交感神经系统肿瘤,也是最常见的儿童颅外实体瘤,通常在 2 岁以下儿童中检出。MB 起源于小脑,是幼儿期致死率最高的脑肿瘤之一。两种肿瘤的发生机制存在一定相似性,且均常出现治疗耐药和预后不良。高危(HR)患者需要接受大剂量联合化疗,但会产生急性和长期毒性。纳米医学和细胞疗法有望改善这些患儿的预后和生活质量。研究已证实,纳米药物可有效降低药物毒性并提高疗效。过去几十年中,这类系统已在癌症研究中得到广泛研究,越来越多用于成人癌症治疗的抗癌纳米载体进入临床。在细胞治疗策略中,临床进展最成熟的是针对这两种疾病的嵌合抗原受体(CAR)T 疗法,目前正在 I/II 期临床试验中研究。然而,儿童药物研究不仅受伦理问题限制,也受到高效临床前模型缺乏和临床试验设计不充分的阻碍。本文更新纳米技术和细胞疗法治疗主要神经系统胚胎性肿瘤的进展,并讨论这一特定领域临床前研究与临床试验之间差距背后的关键问题,同时提出改善临床转化和促进发展的方向。
Embryonal tumors of the nervous system are neoplasms predominantly affecting the pediatric population. Among the most common and aggressive ones are neuroblastoma (NB) and medulloblastoma (MB). NB is a sympathetic nervous system tumor, which is the most frequent extracranial solid pediatric cancer, usually detected in children under two. MB originates in the cerebellum and is one of the most lethal brain tumors in early childhood. Their tumorigenesis presents some similarities and both tumors often have treatment resistances and poor prognosis. High-risk (HR) patients require high dose chemotherapy cocktails associated with acute and long-term toxicities. Nanomedicine and cell therapy arise as potential solutions to improve the prognosis and quality of life of children suffering from these tumors. Indeed, nanomedicines have been demonstrated to efficiently reduce drug toxicity and improve drug efficacy. Moreover, these systems have been extensively studied in cancer research over the last few decades and an increasing number of anticancer nanocarriers for adult cancer treatment has reached the clinic. Among cell-based strategies, the clinically most advanced approach is chimeric-antigen receptor (CAR) T therapy for both pathologies, which is currently under investigation in phase I/II clinical trials. However, pediatric drug research is especially hampered due not only to ethical issues but also to the lack of efficient pre-clinical models and the inadequate design of clinical trials. This review provides an update on progress in the treatment of the main embryonal tumors of the nervous system using nanotechnology and cell-based therapies and discusses key issues behind the gap between preclinical studies and clinical trials in this specific area. Some directions to improve their translation into clinical practice and foster their development are also provided.
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