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[运动系统疾病和神经病变中的抗GM1抗体]

[Anti-Gm1 antibodies in motor system diseases and neuropathies].

作者信息

Thomas F P

机构信息

Neurologisches Institut, Columbia Universität, New York City, NY.

出版信息

Nervenarzt. 1990 Dec;61(12):704-10.

PMID:2079981
Abstract

Increased serum titers of antibodies against the ganglioside GM1 or its carbohydrate epitope Gal(B1-3)GalNAc have been associated with motor neuron disease, motor neuropathies with or without conduction block and sensorimotor neuropathies, whereas low level titers are part of the normal immune repertoire and are present in control groups and in neonatal blood. The target antigens of the antibodies are widely distributed and highly concentrated in the peripheral and central nervous system. The antibodies could damage neural tissue at several anatomic sites. Possible binding sites are the anterior horn cells in the spinal cord and the nodes of Ranvier. Reduction of serum titers with chemotherapy or plasmapheresis can lead to clinical improvement.

摘要

针对神经节苷脂GM1或其碳水化合物表位Gal(β1-3)GalNAc的血清抗体滴度升高,与运动神经元病、伴有或不伴有传导阻滞的运动神经病以及感觉运动神经病有关,而低滴度是正常免疫组成的一部分,存在于对照组和新生儿血液中。抗体的靶抗原广泛分布且高度集中于外周和中枢神经系统。这些抗体可在多个解剖部位损害神经组织。可能的结合部位是脊髓前角细胞和郎飞结。化疗或血浆置换降低血清滴度可导致临床症状改善。

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1
[Anti-Gm1 antibodies in motor system diseases and neuropathies].[运动系统疾病和神经病变中的抗GM1抗体]
Nervenarzt. 1990 Dec;61(12):704-10.
2
Antibodies to GM1 and Gal(beta 1-3)GalNAc at the nodes of Ranvier in human and experimental autoimmune neuropathy.人类及实验性自身免疫性神经病中朗飞结处GM1和Gal(β1-3)GalNAc的抗体
Microsc Res Tech. 1996 Aug 15;34(6):536-43. doi: 10.1002/(SICI)1097-0029(19960815)34:6<536::AID-JEMT5>3.0.CO;2-H.
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Invited review: motor neuropathies, motor neuron disorders, and antiglycolipid antibodies.特邀综述:运动神经病、运动神经元疾病与抗糖脂抗体
Muscle Nerve. 1991 Oct;14(10):927-36. doi: 10.1002/mus.880141002.
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A treatable multifocal motor neuropathy with antibodies to GM1 ganglioside.一种可治疗的、伴有抗GM1神经节苷脂抗体的多灶性运动神经病。
Ann Neurol. 1988 Jul;24(1):73-8. doi: 10.1002/ana.410240113.
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[Measurement of antiganglioside autoantibodies by immunodot-blot assay: clinical importance in peripheral neuropathies].[通过免疫斑点印迹法检测抗神经节苷脂自身抗体:在外周神经病变中的临床意义]
Ann Biol Clin (Paris). 1999 Sep-Oct;57(5):579-88.
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Lower motor neuron disease in a patient with autoantibodies against Gal(beta 1-3)GalNAc in gangliosides GM1 and GD1b: improvement following immunotherapy.
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Polyclonal IgM anti-GM1 ganglioside antibody in patients with motor neuron disease and variants.运动神经元病及其变异型患者中的多克隆抗GM1神经节苷脂抗体
Ann Neurol. 1990 May;27(5):558-63. doi: 10.1002/ana.410270517.
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Antibodies to GM1 and GD1b in patients with motor neuron disease without plasma cell dyscrasia.无浆细胞发育异常的运动神经元病患者体内针对GM1和GD1b的抗体
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Lower motor neuron syndromes defined by patterns of weakness, nerve conduction abnormalities, and high titers of antiglycolipid antibodies.下运动神经元综合征由肌无力模式、神经传导异常和高滴度抗糖脂抗体所定义。
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Motor neuron syndrome and monoclonal IgM with antibody activity against gangliosides GM1 and GD1b.
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