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Immunotherapy in Peripheral Neuropathies
被引:20
|作者:
Leger, Jean-Marc
[1
,2
]
Guimaraes-Costa, Raquel
[1
,2
]
Muntean, Cristina
[1
,2
]
机构:
[1] Univ Hosp Pitie Salpetriere, Inst Hosp Univ Neurosci, Natl Referral Ctr Rare Neuromuscular Dis, Paris, France
[2] Univ Paris 06, Paris, France
关键词:
Immune-mediated neuropathies;
Guillain-Barre syndrome;
Chronic inflammatory demyelinating polyradiculoneuropathy;
Multifocal motor neuropathy;
IgManti-myelin-associated-glycoprotein neuropathy;
Immunomodulatory treatments;
MULTIFOCAL MOTOR NEUROPATHY;
INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY;
GUILLAIN-BARRE-SYNDROME;
INTRAVENOUS IMMUNE GLOBULIN;
PLACEBO-CONTROLLED TRIAL;
LONG-TERM THERAPY;
SUBCUTANEOUS IMMUNOGLOBULIN;
DOUBLE-BLIND;
INTERFERON BETA-1A;
RITUXIMAB;
D O I:
10.1007/s13311-015-0401-7
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Immunotherapy has been investigated in a small subset of peripheral neuropathies, including an acute one, Guillain-Barre syndrome, and 3 chronic forms: chronic inflammatory demyelinating polyradiculoneuropathy, multifocal motor neuropathy, and neuropathy associated with IgM anti-myelin-associated glycoprotein. Several experimental studies and clinical data are strongly suggestive of an immune-mediated pathogenesis. Either cell-mediated mechanisms or antibody responses to Schwann cell, compact myelin, or nodal antigens are considered to act together in an aberrant immune response to cause damage to peripheral nerves. Immunomodulatory treatments used in these neuropathies aim to act at various steps of this pathogenic process. However, there are many phenotypic variants and, consequently, there is a significant difference in the response to immunotherapy between these neuropathies, as well as a need to improve our knowledge and long-term management of chronic forms.
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页码:96 / 107
页数:12
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