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Stage of development
Preclinical in vivo

Intellectual property
PCT patent application

Intended collaboration
Licensing and/or co-development

Contact
Eva Gabaldón
Vice-presidency for Innovation and Transfer
eva.gabaldon@csic.es
comercializacion@csic.es

Reference
CSIC/EG/128
Additional information
#Health #Therapy #Peptide / Protein #Immunology

IFN-I inhibitor for interferonopathies treatment

Inhibitor of Interferon type I (IFN-I) is capable of inhibiting the inflammatory response in those autoimmune diseases in which this cytokine is involved, called interferonopathies, such as systemic lupus erythematosus and Aicardi-Goutières syndrome.

Market need
Interferonopathies are a group of rheumatic diseases that are often severe and have an early onset. The failure of current therapies for their treatment, including monoclonal antibodies against IFN-I and IFNAR, necessitates the investigation of new molecules that can block IFN-I.


Proposed solution
Knowing that viruses have optimized their immunomodulatory mechanisms during millions of years of evolution with their hosts and taking advantage of their characteristics, it has developed an inhibitor from Vaccinia virus that is able to bind IFN-I and block its effects in vitro. Soluble receptors are not currently used in the clinic to inhibit IFN-I, which gives it a great advantage.

Competitive advantages
  • It has 20 times lower immunogenicity than viral proteins.
  • While a monoclonal antibody inhibits only one type of IFN-I, this inhibitor is effective against multiple types of IFN-I.
  • It is soluble.
  • It can be easily humanized.