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Anti lingo 1 (opicinumab) a new monoclonal antibody tested in relapsing remitting multiple sclerosis.

AbstractINTRODUCTION:
Multiple sclerosis (MS) is a chronic demyelinating disease of the central nervous system (CNS). The modern treatment era for MS witnessed a growing pool of drugs now available for use in clinical practice. These therapies work at different levels, however there is a lack of treatments acting on the neurodegenerative component or improving mechanism of repair. Areas covered: The latest knowledge about the pathophysiological changes occurring in MS have translated into novel treatments at different stages of development. Drugs for MS work mainly through modulating the inflammatory factors of the disease, but enhancing remyelination may be more successful in reducing long-term disability. Anti-LINGO-1 (opicinumab) is the first investigational product that achieved phase I trial with the aim of remyelination and axonal protection and/or repair in MS. Expert commentary: Over the past decade considerable strength has been applied to find more reliable strategies to improve myelin repair. The anti-LINGO-1 trial showed that the drug is safe and tolerable. A future phase II trial will provide more insights regarding the compound. The greatest challenge for myelin repair therapies will be how to monitor their efficacy. Eventually research will need to focus on consistent tools to assess the grade of remyelination in vivo.
AuthorsSerena Ruggieri, Carla Tortorella, Claudio Gasperini
JournalExpert review of neurotherapeutics (Expert Rev Neurother) Vol. 17 Issue 11 Pg. 1081-1089 (Nov 2017) ISSN: 1744-8360 [Electronic] England
PMID28885860 (Publication Type: Journal Article, Review)
Chemical References
  • Antibodies, Monoclonal
  • Immunologic Factors
  • LINGO1 protein, human
  • Membrane Proteins
  • Nerve Tissue Proteins
  • opicinumab
Topics
  • Antibodies, Monoclonal (pharmacology)
  • Humans
  • Immunologic Factors (pharmacology)
  • Membrane Proteins (immunology)
  • Multiple Sclerosis, Relapsing-Remitting (drug therapy)
  • Nerve Tissue Proteins (immunology)

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