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髓磷脂肽与维生素D的结合可预防自身免疫性脑脊髓炎的发展。

Association of myelin peptide with vitamin D prevents autoimmune encephalomyelitis development.

作者信息

Mimura L A N, Chiuso-Minicucci F, Fraga-Silva T F C, Zorzella-Pezavento S F G, França T G D, Ishikawa L L W, Penitenti M, Ikoma M R V, Sartori A

机构信息

Department of Microbiology and Immunology, Institute of Biosciences of Botucatu, Univ. Estadual Paulista (UNESP), Distrito de Rubião Junior, Botucatu, São Paulo 18618-970, Brazil.

Flow Cytometry Laboratory - Dr. Amaral Carvalho Foundation, Rua Dona Silvéria, 150, Jaú, São Paulo 17210-070, Brazil.

出版信息

Neuroscience. 2016 Mar 11;317:130-40. doi: 10.1016/j.neuroscience.2015.12.053. Epub 2016 Jan 4.

Abstract

Multiple sclerosis is a chronic, inflammatory and demyelinating disease of the central nervous system (CNS). As there is no cure for this disease, new therapeutic strategies and prophylactic measures are necessary. We recently described the therapeutic activity of the association between myelin oligodendrocyte glycoprotein peptide (MOG) and active vitamin D3 (VitD) against experimental autoimmune encephalomyelitis (EAE). The objective of this work was to evaluate the prophylactic potential of this association in EAE. C57BL/6 mice were vaccinated with MOG in the presence of VitD and then subjected to EAE induction. Animals were euthanized 7 and 19days after disease induction and the following parameters were evaluated: body weight, clinical score, inflammatory process in the CNS, amount of dendritic cells (DCs) and regulatory T cells in the spleen and cytokine production by spleen and CNS cell cultures. Vaccination with MOG associated with VitD determined a drastic reduction in clinical score, body weight loss, CNS inflammation, DCs maturation and also in the production of cytokines by CNS and spleen cell cultures. Collectively, our data indicate that this association prevents EAE development. A similar effect from specific self-antigens associated with VitD is expected in other autoimmune conditions and deserves to be experimentally appraised.

摘要

多发性硬化症是一种中枢神经系统(CNS)的慢性、炎症性和脱髓鞘疾病。由于这种疾病无法治愈,因此需要新的治疗策略和预防措施。我们最近描述了髓鞘少突胶质细胞糖蛋白肽(MOG)与活性维生素D3(VitD)联合使用对实验性自身免疫性脑脊髓炎(EAE)的治疗活性。这项工作的目的是评估这种联合用药在EAE中的预防潜力。将C57BL/6小鼠在VitD存在的情况下用MOG进行接种,然后进行EAE诱导。在疾病诱导后7天和19天对动物实施安乐死,并评估以下参数:体重、临床评分、CNS中的炎症过程、脾脏中树突状细胞(DCs)和调节性T细胞的数量以及脾脏和CNS细胞培养物中细胞因子的产生。用与VitD联合的MOG进行接种可显著降低临床评分、体重减轻、CNS炎症、DCs成熟以及CNS和脾脏细胞培养物中细胞因子的产生。总体而言,我们的数据表明这种联合用药可预防EAE的发展。预计在其他自身免疫性疾病中,与VitD联合的特定自身抗体会产生类似的效果,值得进行实验评估。

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