Department of Neurosurgery, UMass Chan Medical School, Worcester, Massachusetts, USA.
Horae Gene Therapy Center, UMass Chan Medical School, Worcester, Massachusetts, USA.
Hum Gene Ther. 2024 Nov;35(21-22):886-895. doi: 10.1089/hum.2024.057. Epub 2024 Nov 8.
Neurological disease due to single-gene defects represents a targetable entity for adeno-associated virus (AAV)-mediated gene therapy. The delivery of AAV-mediated gene therapy to the brain is challenging, owing to the presence of the blood-brain barrier. Techniques in gene transfer, such as convection-enhanced intraparenchymal delivery and image-guided delivery to the cerebrospinal fluid spaces of the brain, have led the field into highly accurate delivery techniques, which provide correction of genetic defects in specific brain regions or more broadly. These techniques commonly use magnetic resonance imaging (MRI), computed tomography, and fluoroscopic guidance. Even more, the neuroimaging changes evaluated by MRI, MR spectroscopy, diffusion tensor imaging, and functional MRI can serve as important biomarkers of therapy effect and overall disease progression. Here, we discuss the role of neuroimaging in delivering AAV vectors and monitoring the effect of gene therapy.
由于单基因缺陷引起的神经疾病是腺相关病毒(AAV)介导的基因治疗的一个可靶向目标。由于血脑屏障的存在,将 AAV 介导的基因治疗递送到大脑是具有挑战性的。基因转移技术,如增强的脑实质内传递和图像引导的脑脊髓液空间传递,使该领域进入了高度精确的传递技术,这些技术可以在特定的脑区或更广泛的范围内纠正遗传缺陷。这些技术通常使用磁共振成像(MRI)、计算机断层扫描和荧光透视引导。更重要的是,通过 MRI、磁共振波谱、弥散张量成像和功能 MRI 评估的神经影像学变化可以作为治疗效果和整体疾病进展的重要生物标志物。在这里,我们讨论了神经影像学在递送 AAV 载体和监测基因治疗效果中的作用。