Are there immunologically treatable motor neuron diseases?

被引:7
作者
Nobile-Orazio, E [1 ]
Carpo, M [1 ]
Meucci, N [1 ]
机构
[1] Univ Milan, Osped Maggiore Policlin, IRCCS,Ctr Dino Ferrari, Dept Neurol Sci,Giorgio Spagnol Serv Clin Neuroim, I-20122 Milan, Italy
来源
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS | 2001年 / 2卷
关键词
amyotrophic lateral sclerosis; motor neuron disease; motor neuropathy; immunosuppressive therapy; monoclonal gammopathy; lymphoma; paraneoplastic disease;
D O I
10.1080/167-146608201300079382
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Several studies have addressed the issue of a possible immunological involvement in the pathogenesis of amyotrophic lateral sclerosis (ALS) or motor neuron disease (MND), particularly when the disease was associated with cancer, lymphoma or other monoclonal gammopathies or with the presence of serum antibodies to neural antigens. The hypothesis of the existence of immunologically treatable MND was reinforced by the occasional report of MND patients responding to immune or cytostatic therapies and by the identification among those with a purely lower motor neuron syndrome (LMNS) of a motor neuropathy, presently known as multifocal motor neuropathy (MMN), which almost invariably responded to immune therapies. These observations have led to several attempts to treat patients with MND or LMNS, either idiopathic or associated with the above mentioned conditions, with a number of immune or cytostatic therapies. The aim of this review is to verify whether the available data provide enough evidence to support the concept of dysimmune MND and to justify the use in these patients of potentially harmful immune cytostatic therapies.
引用
收藏
页码:S23 / S30
页数:8
相关论文
共 105 条
[1]  
American Association of Electrodiagnostic Medicine Olney R. Guidelines in electrodiagnostic medicine, 1999, MUSCLE NERVE S8, V8, pS225
[2]  
APPEL SH, 2000, AMYOTROPH LATERAL SC, P309
[3]   Immunoassays fail to detect antibodies against neuronal calcium channels in amyotrophic lateral sclerosis serum [J].
Arsac, C ;
Raymond, C ;
MartinMoutot, N ;
Dargent, B ;
Couraud, F ;
Pouget, J ;
Seagar, M .
ANNALS OF NEUROLOGY, 1996, 40 (05) :695-700
[4]   INTRAVENOUS IMMUNOGLOBULIN TREATMENT IN PATIENTS WITH MOTOR-NEURON SYNDROMES ASSOCIATED WITH ANTI-GM1 ANTIBODIES - A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY [J].
AZULAY, JP ;
BLIN, O ;
POUGET, J ;
BOUCRAUT, J ;
BILLETURC, F ;
CARLES, G ;
SERRATRICE, G .
NEUROLOGY, 1994, 44 (03) :429-432
[5]   Multifocal motor neuropathy mimicking motor neuron disease:: nine cases [J].
Bentes, C ;
de Carvalho, M ;
Evangelista, T ;
Sales-Luís, ML .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 169 (1-2) :76-79
[6]   Multifocal motor neuropathy [J].
Biessels, GJ ;
Franssen, H ;
vandenBerg, LH ;
Gibson, A ;
Kappelle, LJ ;
Venables, GS ;
Wokke, JHJ .
JOURNAL OF NEUROLOGY, 1997, 244 (03) :143-152
[7]   MOTOR NEUROPATHY WITH ACTIVITY OF MONOCLONAL IGM ANTIBODY TO GD1A GANGLIOSIDE [J].
BOLLENSEN, E ;
SCHIPPER, HI ;
STECK, AJ .
JOURNAL OF NEUROLOGY, 1989, 236 (06) :353-355
[8]  
BRAIN WR, 1965, BRAIN, V88, P479
[9]  
BRAIN WR, 1963, LANCET, V1, P179
[10]  
BRAIN WR, 1958, LANCET, V2, P271