Suppr超能文献

多发性硬化症治疗:当前生物医学工程方法综述。

Multiple sclerosis treatments a review of current biomedical engineering approaches.

机构信息

Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.

Division of Hematology and Oncology, Department of Internal Medicine, University of Texas Southwestern, Dallas, TX, 75390, USA.

出版信息

Biomaterials. 2025 Feb;313:122807. doi: 10.1016/j.biomaterials.2024.122807. Epub 2024 Sep 3.

Abstract

Multiple Sclerosis (MS) is an autoimmune condition targeting the central nervous system (CNS) characterized by focal demyelination with inflammation, causing neurodegeneration and gliosis. This is accompanied by a refractory period in relapsing MS or chronic progression in primary progressive MS. Current MS treatments target disease relapses and aim to reduce further demyelination and disability. These include the treatment of acute exacerbations through global immunomodulation upon corticosteroid administration, which are accompanied by adverse reactions. Disease modifying therapies (DMTs) which provide targeted immunosuppression of T and B cells, and sequestration of leukocytes out of CNS, have led to further improvements in demyelination prevention and disease burden reduction. Despite their efficacy, DMTs are ineffective in remyelination, pathology reversal and have minimal effects in progressive MS. The advent of modern biomedical engineering approaches in combination with a better understanding of MS pathology, has led to the development of novel, regenerative approaches to treatment. Such treatments utilize neural stem cells (NSCs) and can reduce disease relapses and reverse damage caused by the disease through localized tissue regeneration. While at initial stages, pre-clinical and clinical studies utilizing NSCs and immune modulation have shown promising outcomes in tissue regeneration, creating a potential new era in MS therapy.

摘要

多发性硬化症(MS)是一种自身免疫性疾病,针对中枢神经系统(CNS),其特征是炎症导致的局灶性脱髓鞘,引起神经退行性变和神经胶质增生。这伴随着复发型 MS 的缓解期或原发性进展型 MS 的慢性进展期。目前的 MS 治疗方法针对疾病复发,旨在减少进一步的脱髓鞘和残疾。这些治疗方法包括通过皮质类固醇给药进行全身免疫调节来治疗急性恶化,这伴随着不良反应。疾病修正疗法(DMTs)通过靶向 T 和 B 细胞的免疫抑制以及将白细胞隔离出中枢神经系统,进一步改善了脱髓鞘的预防和疾病负担的减轻。尽管它们具有疗效,但 DMTs 在髓鞘再生、病理逆转方面无效,对进展型 MS 的影响也很小。现代生物医学工程方法的出现以及对 MS 病理的更好理解,导致了治疗的新型再生方法的发展。这些治疗方法利用神经干细胞(NSCs),通过局部组织再生,减少疾病复发并逆转疾病引起的损伤。虽然处于初始阶段,但利用 NSCs 和免疫调节的临床前和临床研究已经显示出在组织再生方面有前景的结果,为 MS 治疗开创了一个潜在的新时代。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验