Treatment and treatment trials in multiple sclerosis

被引:42
作者
Kieseier, Bernd C.
Wiendl, Heinz
Hemmer, Bernhard
Hartung, Hans-Peter
机构
[1] Univ Dusseldorf, Dept Neurol, D-40225 Dusseldorf, Germany
[2] Univ Wurzburg, Dept Neurol, D-8700 Wurzburg, Germany
关键词
CC chemokine receptor 1; clinically isolated syndrome; daclizumab; early treament; glatiramer acetate; interferon beta; intravenous immunoglobulins; natalizumab; rituximab; FTY720;
D O I
10.1097/WCO.0b013e3281568b80
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose of review This review focuses on advances in current and novel treatment approaches in multiple sclerosis. Recent findings New therapeutic approaches in multiple sclerosis are emerging. Orally available treatment strategies are more acceptable for patients and may improve adherence to therapy. An oral formulation of glatiramer acetate failed to demonstrate efficacy in a clinical trial, but other promising compounds are on the horizon, such as FTY720. Advances are currently being made in use of therapeutic monoclonal antibodies that specifically target key molecules involved in the immunopathogenesis of multiple sclerosis. Natalizumab directed against the adhesion molecule very late antigen-4 represents the first specific antibody to be added to our therapeutic armamentarium for multiple sclerosis. Further evidence that immunomodulation should be initiated as early as possible has been reported. Summary Treatment of multiple sclerosis has changed dramatically over the past decade. Enhanced understanding of the immunopathological processes that underlie the disease, advances in biotechnology and development of powerful magnetic resonance imaging technologies, together with improvements in clinical trial design have led to a variety of valuable therapeutic approaches, which are currently being studied in detail.
引用
收藏
页码:286 / 293
页数:8
相关论文
共 85 条
[1]   Intravenous immunoglobulin treatment following the first demyelinating event suggestive of multiple sclerosis - A randomized, double-blind, placebo-controlled trial [J].
Achiron, A ;
Kishner, T ;
Sarova-Pinhas, I ;
Raz, H ;
Faibel, M ;
Stern, Y ;
Lavie, M ;
Gurevich, M ;
Dolev, M ;
Magalashvili, D ;
Barak, Y .
ARCHIVES OF NEUROLOGY, 2004, 61 (10) :1515-1520
[2]   Intravenous immunoglobulin treatment in multiple sclerosis - Effect on relapses [J].
Achiron, A ;
Gabbay, U ;
Gilad, R ;
Hassin-Baer, S ;
Barak, Y ;
Gornish, M ;
Elizur, A ;
Goldhammer, Y ;
Sarova-Pinhas, I .
NEUROLOGY, 1998, 50 (02) :398-402
[3]   Regulatory CD56bright natural killer cells mediate immunomodulatory effects of IL-2Rα-targeted therapy (daclizumab) in multiple sclerosis [J].
Bielekova, B ;
Catalfamo, M ;
Reichert-Scrivner, S ;
Packer, A ;
Cerna, M ;
Waldmann, TA ;
McFarland, H ;
Henkart, PA ;
Martin, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (15) :5941-5946
[4]   Humanized anti-CD25 (daclizumab) inhibits disease activity in multiple sclerosis patients failing to respond to interferon β [J].
Bielekova, B ;
Richert, N ;
Howard, T ;
Blevins, G ;
Markovic-Plese, S ;
McCartin, J ;
Würfel, J ;
Ohayon, J ;
Waidmann, TA ;
McFarland, HF ;
Martin, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (23) :8705-8708
[5]   Acute axonal injury in multiple sclerosis -: Correlation with demyelination and inflammation [J].
Bitsch, A ;
Schuchardt, J ;
Bunkowski, S ;
Kuhlmann, T ;
Brück, W .
BRAIN, 2000, 123 :1174-1183
[6]   A longitudinal study of abnormalities on MRI and disability from multiple sclerosis [J].
Brex, PA ;
Ciccarelli, O ;
O'Riordan, JI ;
Sailer, M ;
Thompson, AJ ;
Miller, DH .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (03) :158-164
[7]   FTY720: Mechanism of action and potential benefit in organ transplantation [J].
Brinkmann, V .
YONSEI MEDICAL JOURNAL, 2004, 45 (06) :991-997
[8]  
Budde K, 2002, J AM SOC NEPHROL, V13, DOI 10.1681/ASN.V1341073
[9]   Mechanisms of disease - The many roles of chemokines and chemokine receptors in inflammation [J].
Charo, IF ;
Ransohoff, RM .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (06) :610-621
[10]   FTY720, a new class of immunomodulator, inhibits lymphocyte egress from secondary lymphoid tissues and thymus by agonistic activity at sphingosine 1-phosphate receptors [J].
Chiba, K .
PHARMACOLOGY & THERAPEUTICS, 2005, 108 (03) :308-319