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为多发性硬化症的有效治疗铺平道路:细胞疗法的进展。

Paving the way towards an effective treatment for multiple sclerosis: advances in cell therapy.

机构信息

Division of Immunology, LCMN, Germans Trias i Pujol University Hospital and Research Institute, Barcelona, Spain.

Department of Cellular Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, Bellaterra, Spain.

出版信息

Cell Mol Immunol. 2021 Jun;18(6):1353-1374. doi: 10.1038/s41423-020-00618-z. Epub 2021 May 6.

Abstract

Multiple sclerosis (MS) is a leading cause of chronic neurological disability in young to middle-aged adults, affecting ~2.5 million people worldwide. Currently, most therapeutics for MS are systemic immunosuppressive or immunomodulatory drugs, but these drugs are unable to halt or reverse the disease and have the potential to cause serious adverse events. Hence, there is an urgent need for the development of next-generation treatments that, alone or in combination, stop the undesired autoimmune response and contribute to the restoration of homeostasis. This review analyzes current MS treatments as well as different cell-based therapies that have been proposed to restore homeostasis in MS patients (tolerogenic dendritic cells, regulatory T cells, mesenchymal stem cells, and vaccination with T cells). Data collected from preclinical studies performed in the experimental autoimmune encephalomyelitis (EAE) model of MS in animals, in vitro cultures of cells from MS patients and the initial results of phase I/II clinical trials are analyzed to better understand which parameters are relevant for obtaining an efficient cell-based therapy for MS.

摘要

多发性硬化症(MS)是中青年人群中慢性神经功能障碍的主要原因,影响全球约 250 万人。目前,大多数 MS 的治疗方法是系统性免疫抑制或免疫调节药物,但这些药物无法阻止或逆转疾病,并有引发严重不良反应的风险。因此,迫切需要开发新一代的治疗方法,这些方法单独或联合使用,可阻止不必要的自身免疫反应,并有助于恢复体内平衡。本综述分析了目前的 MS 治疗方法以及已提出的不同基于细胞的疗法,这些疗法旨在恢复 MS 患者的体内平衡(耐受性树突状细胞、调节性 T 细胞、间充质干细胞和 T 细胞疫苗接种)。分析了从动物 MS 实验性自身免疫性脑脊髓炎(EAE)模型中的临床前研究、MS 患者体外培养细胞中收集的数据以及 I/II 期临床试验的初步结果,以更好地了解哪些参数与获得有效的 MS 基于细胞的治疗方法相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78c6/8167140/ae50e9a94623/41423_2020_618_Fig1_HTML.jpg

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