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T cell receptor altered peptide ligands of Myelin Basic Protein and Proteolipid Protein (Linear and Cyclic) can modulate immune responses in SJL/J mice: Bioactive peptides for Multiple Sclerosis

机译:T细胞受体改变髓鞘碱性蛋白质和蛋白质(线性和环状)的肽配体可以调节SJL / J小鼠中的免疫应答:用于多发性硬化的生物活性肽

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Multiple Sclerosis (MS) is commonly occurring chronic, inflammatory and disabling disorder of the central nervous system (CNS). It affects 0.05-0.15% of Caucasians with the onset of the disease in young adulthood and women with the disease outnumber men two to one [1]. CD4+ type 1 T helper cells are widely considered to play a pivotal pathological role in mediating an autoimmune attack against components of myelin sheath. Recent studies have challenged the idea that more cells, such as CD8+ T cells, macrophages and complement are also responsible for axonal damage and neurodegeneration [2-5]. Myelin Basic Protein (MBP), Proteolipid Protein (PLP) and Myelin Oligodendrocyte Glycoprotein (MOG), have been demonstrated to be encephalitogenic in humans and rodents [5].
机译:多发性硬化症(MS)通常发生慢性,炎症和中枢神经系统(CNS)的疾病。它影响了0.05-0.15%的高加索人,在年轻的成年期和患有疾病的女性中的疾病的疾病两到一[1]。 CD4 +型1 T辅助细胞被广泛认为在介导自身免疫攻击对髓鞘组分的介导自身免疫攻击方面发挥枢轴病理作用。最近的研究挑战了更多的观点,即更多细胞,例如CD8 + T细胞,巨噬细胞和补体也负责轴突损伤和神经变性[2-5]。已经证明,髓鞘碱性蛋白(MBP),蛋白质蛋白(PLP)和髓鞘寡核苷酸糖蛋白(MOG)是人类和啮齿动物中的脑内和啮齿动物[5]。

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