The future of multiple sclerosis therapy

被引:25
作者
Kieseier, Bernd C. [1 ]
Wiendl, Heinz [2 ]
Hartung, Hans-Peter [1 ]
Stueve, Olaf [3 ,4 ]
机构
[1] Univ Dusseldorf, Dept Neurol, D-40225 Dusseldorf, Germany
[2] Univ Wurzburg, Dept Neurol, D-90780 Wurzburg, Germany
[3] VA N Texas Hlth Care Syst, Med Serv, Neurol Sect, Dallas, TX USA
[4] Univ Texas SW Med Ctr Dallas, Dept Neurol, Dallas, TX 75390 USA
关键词
Multiple sclerosis; Immunomodulation; Immunosuppression; Oral therapy; Injectables; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; SPHINGOSINE 1-PHOSPHATE RECEPTORS; DISEASE-MODIFYING THERAPIES; ORAL FINGOLIMOD FTY720; CONTROLLED PHASE IIB; PROGRESSIVE MS; DOUBLE-BLIND; LAQUINIMOD ABR-215062; CLADRIBINE; IMMUNOMODULATOR;
D O I
10.1016/j.phrs.2009.03.016
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Multiple sclerosis (MS) represents the prototypic inflammatory autoimmune disorder of the central nervous system and the most common cause of neurological disability in young adults, exhibiting considerable clinical, radiological and pathological heterogeneity. A better understanding of the immunopathological processes underlying this disease have recently led to the design of numerous novel therapeutical approaches. Perhaps most importantly, therapy has changed dramatically over the past decade in that all relapsing forms of MS, including early forms of MS are now being treated relatively aggressively. However, there are still unmet needs in the management of this disease, especially since all of the currently available disease-modifying drugs are only partially effective. Most of the clinically relevant therapeutic agents are not yet available as oral formulations. A substantial number of pivotal and preliminary reports provide encouraging new evidence on advances being made in the development of oral therapies for MS. A different strategy is the development of very potent monoclonal antibodies, given intravenously or subcutaneously, many of which are being examined for clinical efficacy. These agents are potentially more effective, but may carry more serious side effects. Finally, drugs with a known good safety profile are being developed further. These advances are critically reviewed and put into perspective. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:207 / 211
页数:5
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