Therapies for multiple sclerosis: translational achievements and outstanding needs

被引:76
作者
Haghikia, Aiden [1 ,2 ,3 ]
Hohlfeld, Reinhard [4 ,5 ]
Gold, Ralf [3 ]
Fugger, Lars [1 ,2 ,6 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England
[2] Univ Oxford, John Radcliffe Hosp, MRC Human Immunol Unit, Weatherall Inst Mol Med, Oxford OX3 9DU, England
[3] Ruhr Univ Bochum, St Josef Hosp, Dept Neurol, Bochum, Germany
[4] Univ Munich, Inst Clin Neuroimmunol, Munich, Germany
[5] Munich Cluster Syst Neurol SyNergy, Munich, Germany
[6] Aarhus Univ Hosp, Inst Clin, DK-8000 Aarhus, Denmark
关键词
multiple sclerosis; IFN beta; glatiramer acetate; TNF receptor 1; dimethyl fumarate monoclonal antibodies; PLACEBO-CONTROLLED TRIAL; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; MESENCHYMAL STEM-CELLS; DOUBLE-BLIND; GLATIRAMER ACETATE; INTERFERON BETA-1A; CONTROLLED PHASE-3; INTRAMUSCULAR INTERFERON; DISEASE-ACTIVITY; NATALIZUMAB TREATMENT;
D O I
10.1016/j.molmed.2013.03.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In recent years, multiple sclerosis (MS) research has progressed on several fronts, prompting numerous clinical trials, primarily for immunotherapeutics. Although several new therapies have been disappointing and some were revealed to have devastating side effects, others have shown benefits and all have generated valuable knowledge about the progression of MS, the key contributors to pathogenesis, and on natural surveillance mechanisms for brain infections. This makes now a useful time to take stock of recent advances in developing MS treatments and consider new approaches for adding information where the gaps are greatest - mainly in understanding the degenerative processes responsible for most of the long-term disability. Here, we summarize currently accepted therapeutic principles and the drugs in late stages of development, as well as spotlighting potential novel openings for future research.
引用
收藏
页码:309 / 319
页数:11
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