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髓鞘相关少突胶质细胞碱性蛋白:致脑炎性表位的鉴定及其与多发性硬化症的关联

Myelin-associated oligodendrocytic basic protein: identification of an encephalitogenic epitope and association with multiple sclerosis.

作者信息

Holz A, Bielekova B, Martin R, Oldstone M B

机构信息

Viral-Immunobiology Laboratory, Division of Virology, Department of Neuropharmacology, The Scripps Research Institute, La Jolla, CA 92037, USA.

出版信息

J Immunol. 2000 Jan 15;164(2):1103-9. doi: 10.4049/jimmunol.164.2.1103.

Abstract

Myelin-associated oligodendrocytic basic protein (MOBP) is an abundant myelin constituent expressed exclusively by oligodendrocytes, the myelin-forming cells of the CNS. We report that MOBP causes experimental allergic encephalomyelitis and is associated with multiple sclerosis. First, we note that purified recombinant MOBP inoculated into SJL/J mice produces CNS disease. Tests of overlapping peptides spanning the murine MOBP molecule map the encephalitogenic site to amino acids 37-60. MOBP-induced experimental allergic encephalomyelitis shows a severe clinical course and is characterized by a prominent CD4+ T lymphocyte infiltration and a lesser presence of CD8+ T cells and microglia/macrophages around vessels and in the white matter of the CNS. Second, PBL obtained from patients with relapsing/remitting multiple sclerosis mount a proliferative response to human MOBP, especially at amino acids 21-39. This response equals or exceeds the response to myelin basic protein and an influenza virus hemagglutinin peptide, both serving as internal controls. Thus, a novel myelin Ag, MOBP aa 37-60, plays a role in rodent autoimmune CNS disease, and its human MOBP counterpart is associated with the human demyelinating disease multiple sclerosis.

摘要

髓鞘相关少突胶质细胞碱性蛋白(MOBP)是一种仅由少突胶质细胞表达的丰富的髓鞘成分,少突胶质细胞是中枢神经系统中形成髓鞘的细胞。我们报告MOBP可引发实验性变应性脑脊髓炎,并与多发性硬化症相关。首先,我们注意到接种到SJL/J小鼠体内的纯化重组MOBP会引发中枢神经系统疾病。对跨越鼠MOBP分子的重叠肽段进行检测,将致脑炎位点定位到氨基酸37 - 60。MOBP诱导的实验性变应性脑脊髓炎呈现出严重的临床病程,其特征为明显的CD4 + T淋巴细胞浸润,且在中枢神经系统血管周围和白质中CD8 + T细胞以及小胶质细胞/巨噬细胞的存在较少。其次,从复发/缓解型多发性硬化症患者获取的外周血淋巴细胞对人MOBP产生增殖反应,尤其是对氨基酸21 - 39处的反应。这种反应等同于或超过对髓鞘碱性蛋白和流感病毒血凝素肽段的反应,二者均作为内部对照。因此,一种新的髓鞘抗原,即MOBP氨基酸37 - 60,在啮齿动物自身免疫性中枢神经系统疾病中起作用,并且其在人类中的对应物与人脱髓鞘疾病多发性硬化症相关。

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