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Therapeutic Exosomes for Multiple Sclerosis and Other Demyelinating Diseases

Interests: Neurology
Published:
Lead Inventor: Richard Kraig

SUMMARY

  • Multiple Sclerosis (MS) is caused by degradation of the protective myelin sheath that surrounds nerve fibers in the brain and spinal cord. Current MS therapies only stop the progression of this demyelination and do not promote the repair of the myelin sheath, which significantly limits their efficacy.
  • The invention is a novel method for generating exosome-based therapies for the treatment of demyelinating disease, including MS. The inventors demonstrated that exosomes derived from dendritic cells can cross the blood brain barrier when delivered intranasally, relieve oxidative stress, and increase baseline myelination with no observable toxicity. 
  • Therapeutic exosomes are preferentially absorbed by oligodendrocytes, the cells that myelinate central nervous system axons, and contain specific micro-RNA that are known to increase myelin formation. In vitro studies show that therapeutic exosomes can remeylinate damaged brain slice cultures.

FIGURE

(A) Treatment of hippocampal slice cultures with dendritic cell exosomes significantly increased remyelination five days after lysolecithin injury, compared to controls. (B-C) Nasal delivery of exosomes to rats increased myelin levels over baseline. MBP= myelin basic protein. 

 

 

ADVANTAGES

ADVANTAGES

  • Disease modifying mechanism of action
  • Ex vivo production that does not require patient cells
  • Can be frozen for storage

 

APPLICATIONS

  • Treatment of demyelinating diseases, such as MS, Alzheimer's disease, and migraine.

 

PUBLICATIONS

 

 

  • US: 10,231,997
  • US patent pending: 16/259,563
  • Counterparts issued in Australia and pending in EU and Canada