Simões-Abade Madalena B C, Patterer Marlene, Nicaise Alexandra M, Pluchino Stefano
Department of Clinical Neurosciences and NIHR Biomedical Research Centre, University of Cambridge, Cambridge, United Kingdom.
Front Cell Neurosci. 2024 Dec 18;18:1488691. doi: 10.3389/fncel.2024.1488691. eCollection 2024.
Multiple sclerosis (MS), a debilitating autoimmune disorder targeting the central nervous system (CNS), is marked by relentless demyelination and inflammation. Clinically, it presents in three distinct forms: relapsing-remitting MS (RRMS), primary progressive MS (PPMS), and secondary progressive MS (SPMS). While disease-modifying therapies (DMTs) offer some relief to people with RRMS, treatment options for progressive MS (pMS) remain frustratingly inadequate. This gap highlights an urgent need for advanced disease modeling techniques to unravel the intricate pathology of pMS. Human induced pluripotent stem cell (iPSC) technologies and brain organoids are emerging as promising tools for disease modeling in both 2D and 3D environments. These innovative approaches enable the study of disease mechanisms that closely mimic human pathophysiology and offer new platforms for screening therapeutic compounds, surpassing the limitations of traditional animal models. However, deploying brain organoids in disease modeling presents challenges, especially in the context of non-monogenic disorders. This review delves into cutting-edge brain organoid techniques that hold the potential to revolutionize our understanding of pMS, offering a pathway to disentangle its underlying mechanisms and drive transformative discoveries.
多发性硬化症(MS)是一种侵袭中枢神经系统(CNS)的使人衰弱的自身免疫性疾病,其特征是持续的脱髓鞘和炎症。在临床上,它表现为三种不同的形式:复发缓解型多发性硬化症(RRMS)、原发进展型多发性硬化症(PPMS)和继发进展型多发性硬化症(SPMS)。虽然疾病修正疗法(DMTs)能为RRMS患者提供一些缓解,但进展型多发性硬化症(pMS)的治疗选择仍然极其不足。这一差距凸显了迫切需要先进的疾病建模技术来揭示pMS错综复杂的病理机制。人类诱导多能干细胞(iPSC)技术和脑类器官正成为二维和三维环境中疾病建模的有前景的工具。这些创新方法能够研究与人类病理生理学密切相似的疾病机制,并为筛选治疗化合物提供新平台,克服了传统动物模型的局限性。然而,在疾病建模中应用脑类器官存在挑战,尤其是在非单基因疾病的背景下。这篇综述深入探讨了前沿的脑类器官技术,这些技术有可能彻底改变我们对pMS的理解,为理清其潜在机制并推动变革性发现提供了一条途径。