CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Engineering focused ultrasound for glioblastoma.
Engineering focused ultrasound for glioblastoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
FUS 提供了一个可调控的多模态平台,具有克服 GBM 核心耐药机制的潜力。通过将 FUS 作为辅助疗法与新兴免疫疗法和靶向药物递送系统相结合,复发性胶质母细胞瘤可得到有效治疗。
聚焦超声(FUS)是一种快速发展的非侵入性能量递送技术,能够通过声波精确调控肿瘤微环境(TME)。胶质母细胞瘤(GBM)以TME深度免疫抑制和治疗抵抗为特征,已成为FUS治疗的关键研究对象。
本综述探讨了FUS的技术演进及其在GBM中扩展的应用,包括低强度和高强度FUS的亚型及其对治疗效果的机制性贡献。
通过PubMed、Scopus和Google Scholar进行了全面的文献综述,以识别在GBM背景下使用FUS的临床前和临床研究。如果文章讨论了FUS机制(热效应、机械效应)、生物效应(免疫调节、屏障通透性、细胞死亡)或联合方法(例如药物递送、CAR-T 细胞、声动力疗法),则纳入这些文章。
文献检索共获得312项研究;95项符合纳入标准(67项临床前研究、14项临床试验、14项综述),具有明确的FUS参数和生物学终点。FUS能够对GBM中的热效应和机械效应进行时空控制。通过调节占空比、声压和暴露时间,FUS可在不同治疗模式下发挥作用。临床前数据支持使用FUS进行靶向药物递送、免疫细胞重极化以及与免疫疗法的协同效应。临床试验证明了多种FUS平台的安全性和可行性。
Focused ultrasound (FUS) is a rapidly advancing noninvasive energy delivery technology with the capacity to precisely modulate the tumor microenvironment (TME) through acoustic waves. Glioblastoma (GBM) is characterized by profound TME immune suppression and treatment resistance and has emerged as a key subject to treatment with FUS therapy.
This review examines the technical evolution of FUS and its expanded applications in GBM, including subtypes of low- and high-intensity FUS and their mechanistic contributions to therapeutic effect.
A comprehensive literature review was conducted using PubMed, Scopus, and Google Scholar to identify preclinical and clinical studies utilizing FUS in the context of GBM. Articles were included if they discussed FUS mechanisms (thermal, mechanical), bioeffects (immunomodulation, barrier permeability, cell death), or combinatory approaches (e.g., drug delivery, CAR T cells, sonodynamic therapy).
A literature search yielded 312 studies; 95 met inclusion criteria (67 preclinical, 14 clinical trials, 14 reviews) with defined FUS parameters and biological endpoints. FUS enables spatiotemporal control of thermal and mechanical effects in GBM. Modulation of duty cycle, acoustic pressure, and exposure time allows FUS to operate across therapeutic regimes. Preclinical data support using FUS for targeted drug delivery, immune cell repolarization, and synergistic effects with immunotherapies. Clinical trials demonstrate the safety and feasibility of several FUS platforms.
FUS offers a tunable multimodal platform with the potential to overcome core resistance mechanisms in GBM. Recurrent glioblastoma could be effectively treated by integrating FUS as an adjunct therapy alongside emerging immunotherapies and targeted drug delivery systems.
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