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
[41]   NEUROLOGICAL DISEASE INDUCED IN TRANSGENIC MICE EXPRESSING THE ENV GENE OF THE CAS-BR-E MURINE RETROVIRUS [J].
KAY, DG ;
GRAVEL, C ;
POTHIER, F ;
LAPERRIERE, A ;
ROBITAILLE, Y ;
JOLICOEUR, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (10) :4538-4542
[42]   INTRAVENOUS IMMUNOGLOBULIN FOR MULTIFOCAL MOTOR NEUROPATHY [J].
KERMODE, AG ;
LAING, BA ;
CARROLL, WM ;
MASTAGLIA, FL .
LANCET, 1992, 340 (8824) :920-921
[43]  
Khwaja S, 1998, MUSCLE NERVE, V21, P943
[44]   CLINICAL AND ELECTROPHYSIOLOGIC CORRELATES OF ELEVATED ANTI-GM(1) ANTIBODY-TITERS [J].
KINSELLA, LJ ;
LANGE, DJ ;
TROJABORG, W ;
SADIQ, SA ;
YOUNGER, DS ;
LATOV, N .
NEUROLOGY, 1994, 44 (07) :1278-1282
[45]   THE CLINICAL AND DIAGNOSTIC ROLE OF ANTI-GM(1) ANTIBODY TESTING [J].
KORNBERG, AJ ;
PESTRONK, A .
MUSCLE & NERVE, 1994, 17 (01) :100-104
[46]  
Kornberg Andrew J., 1995, Annals of Neurology, V37, pS43
[47]   EPIDEMIOLOGY OF AMYOTROPHIC LATERAL SCLEROSIS - .1. A CASE-CONTROL COMPARISON BASED ON ALS DEATHS [J].
KURTZKE, JF ;
BEEBE, GW .
NEUROLOGY, 1980, 30 (05) :453-462
[48]   CLINICAL CORRELATIONS OF ANTI-GM1 ANTIBODIES IN AMYOTROPHIC-LATERAL-SCLEROSIS AND NEUROPATHIES [J].
LAMB, NL ;
PATTEN, BM .
MUSCLE & NERVE, 1991, 14 (10) :1021-1027
[49]   MONOCLONAL IGM WITH UNIQUE SPECIFICITY TO GANGLIOSIDES GM1 AND GD1B AND TO LACTO-N-TETRAOSE ASSOCIATED WITH HUMAN MOTOR NEURON DISEASE [J].
LATOV, N ;
HAYS, AP ;
DONOFRIO, PD ;
LIAO, J ;
ITO, H ;
MCGINNIS, S ;
MANOUSSOS, K ;
FREDDO, L ;
SHY, ME ;
SHERMAN, WH ;
CHANG, HW ;
GREENBERG, HS ;
ALBERS, JW ;
ALESSI, AG ;
KEREN, D ;
YU, RK ;
ROWLAND, LP ;
KABAT, EA .
NEUROLOGY, 1988, 38 (05) :763-768
[50]   MOTOR-NEURON DISEASE AND MONOCLONAL GAMMOPATHY [J].
LAVRNIC, D ;
VIDAKOVIC, A ;
MILETIC, V ;
TRIKIC, R ;
MARINKOVIC, Z ;
RAKOCEVIC, V ;
NIKOLIC, J ;
WIRGUIN, I ;
SADIQ, SA ;
APOSTOLSKI, S .
EUROPEAN NEUROLOGY, 1995, 35 (02) :104-107