New drugs for multiple sclerosis: new treatment algorithms

被引:21
作者
Cree, Bruce A. C. [1 ]
Hartung, Hans-Peter [2 ,3 ,4 ,5 ]
Barnett, Michael [3 ,6 ]
机构
[1] Univ Calif San Francisco, Dept Neurol, UCSF Weill Inst Neurosci, San Francisco, CA USA
[2] Heinrich Heine Univ Dusseldorf, Dept Neurol, Dusseldorf, Germany
[3] Univ Sydney, Brain & Mind Ctr, Sydney, NSW, Australia
[4] Med Univ Vienna, Dept Neurol, Vienna, Austria
[5] Palacky Univ Olomouc, Dept Neurol, Olomouc, Czech Republic
[6] Sydney Neuroimaging Anal Ctr, Sydney, NSW, Australia
关键词
Bruton's tyrosine kinase; clinical trials; disease modifying therapies; multiple sclerosis; remyelination; EPSTEIN-BARR-VIRUS; DISEASE-MODIFYING THERAPY; DOUBLE-BLIND; INTERFERON; ALEMTUZUMAB; DISABILITY; INFECTION; EFFICACY;
D O I
10.1097/WCO.0000000000001063
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 To discuss recent changes in the multiple sclerosis (MS) treatment algorithm and to present therapies currently in MS clinical trials. Recent findings High efficacy disease modifying therapies are optimally beneficial when used in the early, inflammatory phase of MS. Bruton's tyrosine kinase has emerged as an important therapeutic target for both relapsing and progressive forms of MS. Multiple therapies targeting remyelination failed to provide conclusive evidence of broad therapeutic benefit; however, more targeted approaches offer hope that myelin repair might be achieved resulting in specific clinical improvements. Strategies targeting chronic Epstein-Barr virus infection and dysbiosis of the gut microbiome are the first to link microbial risk factors for MS and therapeutic interventions. A striking number of diverse treatments under investigation bodes well for development of better and more effective therapies in MS.
引用
收藏
页码:262 / 270
页数:9
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