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Biotherapies in multiple sclerosis: A step toward remyelination and neuroprotection?
被引:2
作者:

Dubessy, A. -L.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Paris 06, Sorbonne Univ, UMR S 1127, F-75013 Paris, France
INSERM, U1127, F-75013 Paris, France
CNRS, UMR 7225, F-75013 Paris, France
ICM, F-75013 Paris, France Univ Paris 06, Sorbonne Univ, UMR S 1127, F-75013 Paris, France

Zujovic, V.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Paris 06, Sorbonne Univ, UMR S 1127, F-75013 Paris, France
INSERM, U1127, F-75013 Paris, France
CNRS, UMR 7225, F-75013 Paris, France
ICM, F-75013 Paris, France Univ Paris 06, Sorbonne Univ, UMR S 1127, F-75013 Paris, France

Papeix, C.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Paris 06, Sorbonne Univ, UMR S 1127, F-75013 Paris, France
INSERM, U1127, F-75013 Paris, France
CNRS, UMR 7225, F-75013 Paris, France
ICM, F-75013 Paris, France Univ Paris 06, Sorbonne Univ, UMR S 1127, F-75013 Paris, France

Stankoff, B.
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h-index: 0
机构:
Univ Paris 06, Sorbonne Univ, UMR S 1127, F-75013 Paris, France
INSERM, U1127, F-75013 Paris, France
CNRS, UMR 7225, F-75013 Paris, France
ICM, F-75013 Paris, France Univ Paris 06, Sorbonne Univ, UMR S 1127, F-75013 Paris, France
机构:
[1] Univ Paris 06, Sorbonne Univ, UMR S 1127, F-75013 Paris, France
[2] INSERM, U1127, F-75013 Paris, France
[3] CNRS, UMR 7225, F-75013 Paris, France
[4] ICM, F-75013 Paris, France
关键词:
Multiple sclerosis;
Lingo1;
Nogo;
Remyelination;
Stem cells;
Transplantation;
SPINAL-CORD-INJURY;
OLFACTORY ENSHEATHING CELLS;
CENTRAL-NERVOUS-SYSTEM;
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS;
NEURITE OUTGROWTH INHIBITOR;
OLIGODENDROCYTE PROGENITOR CELLS;
MYELINATING SCHWANN-CELLS;
NOGO-A;
FUNCTIONAL RECOVERY;
AXONAL INTEGRITY;
D O I:
10.1016/j.neurol.2014.10.004
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Multiple sclerosis (MS) is a complex disease of the central nervous system (CNS), characterized by CNS-restricted inflammation with subsequent demyelination and neurodegeneration. Current disease-modifying therapies efficiently reduce relapse rate and new lesions appearance, but still fail to impact the progressive course of the disease. There is a great need for the avenue of new therapies aimed at promoting myelin repair or reducing neurodegeneration that should result in the prevention of neurological disability in this chronic disease. This review will focus on the potentials and limitations of biotherapies that are currently developed for the promotion of CNS repair in MS, either monoclonal antibodies targeting axonal growth and remyelination, or cell therapies aimed at replacing the depleted myelinating cells within the CNS. As other researches aimed at promoting neuroprotection or remyelination are following a classical pharmacological approach, they will not be described in this review, which will focus on antibody-based therapies and cell therapies. (C) 2014 Elsevier Masson SAS. All rights reserved.
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页码:770 / 778
页数:9
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