Axonal degeneration in the pathogenesis of multiple sclerosis

被引:81
作者
Silber, E [1 ]
Sharief, MK [1 ]
机构
[1] Kings Coll London, Guys Kings & St Thomas Sch Med, Dept Clin Neurosci, London WC2R 2LS, England
关键词
multiple sclerosis; axon;
D O I
10.1016/S0022-510X(99)00178-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Axonal degeneration plays an important role in the accumulation of disability in patients with multiple sclerosis (MS). Pathological studies have demonstrated axonal damage, particularly in areas of acute inflammation and demyelination, and in chronic lesions. Axonal loss and its progression, which is associated with neurological disability, has also been demonstrated by magnetic resonance imaging (MRI) studies. The mechanisms of axonal loss are uncertain, but may involve axonal degeneration secondary to demyelination, or damage to the axonal cytoskeleton. Inflammatory mediators, including cytokines and proteolytic enzymes may contribute to axonal damage, as may nitric oxide. Axonal destruction may also be due to immune attack directed at axonal components. The realisation that axonal degeneration is a fundamental component of MS that may occur early in the disease course should alter the approach to management and open avenues to a more targeted immunotherapy aimed at reducing the progression of disability. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:11 / 18
页数:8
相关论文
共 97 条
[1]   USE OF PROTON MAGNETIC-RESONANCE SPECTROSCOPY FOR MONITORING DISEASE PROGRESSION IN MULTIPLE-SCLEROSIS [J].
ARNOLD, DL ;
RIESS, GT ;
MATTHEWS, PM ;
FRANCIS, GS ;
COLLINS, DL ;
WOLFSON, C ;
ANTEL, JP .
ANNALS OF NEUROLOGY, 1994, 36 (01) :76-82
[2]   LONGITUDINAL SPINAL-CORD SECTIONS AS SUBSTRATUM FOR ANTI-NEUROFILAMENT ANTIBODY DETECTION [J].
BAHMANYAR, S ;
GAJDUSEK, DC ;
SOTELO, J ;
GIBBS, CJ .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1982, 53 (01) :85-90
[3]   INFLAMMATORY REACTION IN EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS (EAE) IS ACCOMPANIED BY A MICROGLIAL EXPRESSION OF THE BETA-A4-AMYLOID PRECURSOR PROTEIN (APP) [J].
BANATI, RB ;
GEHRMANN, J ;
LANNESVIEIRA, J ;
WEKERLE, H ;
KREUTZBERG, GW .
GLIA, 1995, 14 (03) :209-215
[4]   THE LONGSTANDING MS LESION - A QUANTITATIVE MRI AND ELECTRON-MICROSCOPIC STUDY [J].
BARNES, D ;
MUNRO, PMG ;
YOUL, BD ;
PRINEAS, JW ;
MCDONALD, WI .
BRAIN, 1991, 114 :1271-1280
[5]   A CRUCIAL ROLE FOR NEUROTROPHIN-3 IN OLIGODENDROCYTE DEVELOPMENT [J].
BARRES, BA ;
RAFF, MC ;
GAESE, F ;
BARTKE, I ;
DECHANT, G ;
BARDE, YA .
NATURE, 1994, 367 (6461) :371-375
[6]   PROLIFERATION OF OLIGODENDROCYTE PRECURSOR CELLS DEPENDS ON ELECTRICAL-ACTIVITY IN AXONS [J].
BARRES, BA ;
RAFF, MC .
NATURE, 1993, 361 (6409) :258-260
[7]   HUMAN MONOCLONAL AUTOANTIBODIES PRODUCED BY HYBRIDOMAS DERIVED FROM LYMPHOCYTES OF MULTIPLE-SCLEROSIS PATIENTS [J].
BLANCHER, A ;
OKSMAN, F ;
LYMBERI, P ;
CALVAS, P ;
CAMBONTHOMSEN, A ;
CLANET, M ;
DUCOS, J .
RESEARCH IN IMMUNOLOGY, 1989, 140 (07) :711-724
[8]   INDUCTION OF NITRIC-OXIDE SYNTHASE IN DEMYELINATING REGIONS OF MULTIPLE-SCLEROSIS BRAINS [J].
BO, L ;
DAWSON, TM ;
WESSELINGH, S ;
MORK, S ;
CHOI, S ;
KONG, PA ;
HANLEY, D ;
TRAPP, BD .
ANNALS OF NEUROLOGY, 1994, 36 (05) :778-786
[9]   INDIRECT EVIDENCE FOR NITRIC-OXIDE INVOLVEMENT IN MULTIPLE-SCLEROSIS BY CHARACTERIZATION OF CIRCULATING ANTIBODIES DIRECTED AGAINST CONJUGATED S-NITROSOCYSTEINE [J].
BOULLERNE, AI ;
PETRY, KG ;
MEYNARD, M ;
GEFFARD, M .
JOURNAL OF NEUROIMMUNOLOGY, 1995, 60 (1-2) :117-124
[10]   MOTOR NEURONS AND NEUROFILAMENTS IN SICKNESS AND IN HEALTH [J].
BRADY, ST .
CELL, 1993, 73 (01) :1-3