The Role of Immune and Inflammatory Mechanisms in ALS

被引:3
作者
McCombe, P. A. [1 ]
Henderson, R. D. [1 ]
机构
[1] Univ Queensland, UQ Ctr Clin Res, Herston, Qld 4029, Australia
基金
英国医学研究理事会;
关键词
Amyotrophic lateral sclerosis; biomarkers; immunity; inflammation; lymphocytes; protective immunity; T cells; AMYOTROPHIC-LATERAL-SCLEROSIS; MOTOR-NEURON DISEASE; POSITRON-EMISSION-TOMOGRAPHY; MUTANT SUPEROXIDE-DISMUTASE; CENTRAL-NERVOUS-SYSTEM; UNIT NUMBER ESTIMATION; SPINAL-CORD TISSUE; MOUSE MODEL; SPORADIC ALS; MULTIPLE-SCLEROSIS;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Amyotrophic lateral sclerosis (ALS) is a severe progressive neurodegenerative disease. The cause is unknown, but genetic abnormalities have been identified in subjects with familial ALS and also in subjects with sporadic ALS. Environmental factors such as occupational exposure have been shown to be risk factors for the development of ALS. Patients differ in their clinical features and differ in the clinical course of disease. Immune abnormalities have been found in the central nervous system by pathological studies and also in the blood and CSF of subjects with ALS. Inflammation and immune abnormalities are also found in animals with a model of ALS due to mutations in the SOD1 gene. Previously it has been considered that immune abnormalities might contribute to the pathogenesis of disease. However more recently it has become apparent that an immune response can occur as a response to damage to the nervous system and this can be protective.
引用
收藏
页码:246 / 254
页数:9
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