Ana Isabel Álvarez-López , Nuria Álvarez-Sánchez , Ivan Cruz-Chamorro , Guillermo Santos-Sánchez , Eduardo Ponce-España , Ignacio Bejarano , Patricia Judith Lardone , Antonio Carrillo-Vico
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The most common clinical form of MS is relapsing-remitting (RR), characterized by neuroinflammatory episodes followed by partial or total recovery of neurological deficits. The first-line treatment for RRMS relapses is a high dose of glucocorticoids, especially methylprednisolone, for three to five consecutive days. Several studies have reported the beneficial effects of melatonin in the context of neuroinflammation associated with MS or experimental autoimmune encephalomyelitis (EAE), the preclinical model for MS. Therefore, the objective of this study was to evaluate the effect of the combined treatment of melatonin and methylprednisolone on the neuroinflammatory response associated with the EAE development. This study shows for the first time the protective synergistic effect of co-treatment with melatonin and methylprednisolone on reducing the severity of EAE by decreasing CD4 lymphocytes, B cells, macrophages and dendritic cells in the CNS, as well as modulating the population of infiltrated T and B cells toward regulatory phenotypes to the detriment of pro-inflammatory effector functions. In addition to the potentiation of the protective role of methylprednisolone, treatment with melatonin from the clinical onset of EAE improves the natural course of the EAE and the response to a subsequent treatment with methylprednisolone in a later relapse of the disease, pointing melatonin as potential therapeutic tool in combination with methylprednisolone for the treatment of relapses in MS.</p></div>","PeriodicalId":15245,"journal":{"name":"Journal of autoimmunity","volume":"148 ","pages":"Article 103298"},"PeriodicalIF":7.9000,"publicationDate":"2024-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S089684112400132X/pdfft?md5=951f35a4ccfd85922a4071f095a390df&pid=1-s2.0-S089684112400132X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Melatonin synergistically potentiates the effect of methylprednisolone on reducing neuroinflammation in the experimental autoimmune encephalomyelitis mouse model of multiple sclerosis\",\"authors\":\"Ana Isabel Álvarez-López , Nuria Álvarez-Sánchez , Ivan Cruz-Chamorro , Guillermo Santos-Sánchez , Eduardo Ponce-España , Ignacio Bejarano , Patricia Judith Lardone , Antonio Carrillo-Vico\",\"doi\":\"10.1016/j.jaut.2024.103298\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Multiple sclerosis (MS) is an autoimmune neurodegenerative disease of unknown etiology characterized by infiltration of encephalitogenic cells in the central nervous system (CNS) resulting in the presence of multifocal areas of demyelination leading to neurodegeneration. 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引用次数: 0
摘要
多发性硬化症(MS)是一种病因不明的自身免疫性神经退行性疾病,其特征是中枢神经系统(CNS)中的致脑细胞浸润导致多灶性脱髓鞘区域的存在,从而导致神经退行性疾病。浸润的免疫细胞群主要由效应 CD4 和 CD8 T 淋巴细胞、B 细胞、巨噬细胞和树突状细胞组成,这些细胞分泌促炎因子,最终损伤髓鞘,导致轴突损伤。临床上最常见的多发性硬化症是复发-缓解型(RR),其特点是神经炎症发作后神经功能缺损部分或完全恢复。RRMS 复发的一线治疗是连续三到五天使用大剂量糖皮质激素,尤其是甲基强的松龙。有几项研究报道了褪黑素对多发性硬化症或多发性硬化症临床前模型--实验性自身免疫性脑脊髓炎(EAE)相关神经炎症的有益作用。因此,本研究的目的是评估褪黑素和甲基强的松龙联合治疗对与EAE发展相关的神经炎症反应的影响。这项研究首次显示了褪黑素和甲基强的松龙联合治疗对减轻 EAE 严重程度的保护性协同作用,它能减少中枢神经系统中的 CD4 淋巴细胞、B 细胞、巨噬细胞和树突状细胞,并使浸润的 T 细胞和 B 细胞群向调节表型转化,从而削弱促炎效应功能。除了能增强甲基强的松龙的保护作用外,褪黑素还能在EAE临床发病时就开始治疗,从而改善EAE的自然病程以及在疾病复发时对随后甲基强的松龙治疗的反应,这表明褪黑素是与甲基强的松龙联合治疗多发性硬化症复发的潜在治疗工具。
Melatonin synergistically potentiates the effect of methylprednisolone on reducing neuroinflammation in the experimental autoimmune encephalomyelitis mouse model of multiple sclerosis
Multiple sclerosis (MS) is an autoimmune neurodegenerative disease of unknown etiology characterized by infiltration of encephalitogenic cells in the central nervous system (CNS) resulting in the presence of multifocal areas of demyelination leading to neurodegeneration. The infiltrated immune cells population is composed mainly of effector CD4+ and CD8+ T lymphocytes, B cells, macrophages, and dendritic cells that secrete pro-inflammatory factors that eventually damage myelin leading to axonal damage. The most common clinical form of MS is relapsing-remitting (RR), characterized by neuroinflammatory episodes followed by partial or total recovery of neurological deficits. The first-line treatment for RRMS relapses is a high dose of glucocorticoids, especially methylprednisolone, for three to five consecutive days. Several studies have reported the beneficial effects of melatonin in the context of neuroinflammation associated with MS or experimental autoimmune encephalomyelitis (EAE), the preclinical model for MS. Therefore, the objective of this study was to evaluate the effect of the combined treatment of melatonin and methylprednisolone on the neuroinflammatory response associated with the EAE development. This study shows for the first time the protective synergistic effect of co-treatment with melatonin and methylprednisolone on reducing the severity of EAE by decreasing CD4 lymphocytes, B cells, macrophages and dendritic cells in the CNS, as well as modulating the population of infiltrated T and B cells toward regulatory phenotypes to the detriment of pro-inflammatory effector functions. In addition to the potentiation of the protective role of methylprednisolone, treatment with melatonin from the clinical onset of EAE improves the natural course of the EAE and the response to a subsequent treatment with methylprednisolone in a later relapse of the disease, pointing melatonin as potential therapeutic tool in combination with methylprednisolone for the treatment of relapses in MS.
期刊介绍:
The Journal of Autoimmunity serves as the primary publication for research on various facets of autoimmunity. These include topics such as the mechanism of self-recognition, regulation of autoimmune responses, experimental autoimmune diseases, diagnostic tests for autoantibodies, as well as the epidemiology, pathophysiology, and treatment of autoimmune diseases. While the journal covers a wide range of subjects, it emphasizes papers exploring the genetic, molecular biology, and cellular aspects of the field.
The Journal of Translational Autoimmunity, on the other hand, is a subsidiary journal of the Journal of Autoimmunity. It focuses specifically on translating scientific discoveries in autoimmunity into clinical applications and practical solutions. By highlighting research that bridges the gap between basic science and clinical practice, the Journal of Translational Autoimmunity aims to advance the understanding and treatment of autoimmune diseases.