Ex-vivo Production of Regulatory B-Cells for Use in Auto-immune Diseases


Regulatory B-cells (Breg) play an important role in reducing autoimmunity and reduced levels of these cells are implicated in etiology of several auto-inflammatory diseases. Despite their impact in many diseases, their physiological inducers are unknown.  Given that Bregs are a very rare B-cell, identifying factors that promote their development would allow in vivo modulation of Breg levels and ex-vivo production of large amounts of antigen-specific Bregs to use in immunotherapy for auto-inflammatory diseases.
 
Researchers at NEI's Molecular Immunology Section developed a method for the ex-vivo production of Breg. The method of production involves treating isolated primary B-cells or B-cell lines with IL-35 to induce their conversion into IL-10, producing Breg. Using this method, B-regulatory cells can be produced in large quantity and used in a Breg-based therapy against autoimmune diseases including, but not limited to, uveitis and sarcoidosis. In vivo animal data are available.



Potential Commercial Applications: Competitive Advantages:
  • In vivo modulation of Breg levels
  • Supplement the low population of Breg in a patient suffering from an autoimmune disease where it is known that B-regulatory cell populations are severely reduced (i.e. uveitis)
  • Use in immunotherapy for the treatment of other autoimmune diseases such as multiple sclerosis, sarcoidosis, colitis, and arthritis.
 
  • There is no known biological or chemical agent that can induce Bregs ex-vivo
  • This method produces large quantities of Bregs and can therefore aid in Breg-based therapy
  • Pre-clinical mouse model data available that uses the Bregs to treat experimental autoimmune uveitis (EAU)


Development Stage:
Pre-clinical (in vivo)

Inventors:

Charles Egwuagu (NEI)  ➽ more inventions...

Wang Ren-Xi (NEI)  ➽ more inventions...

Cheng-Rong Yu (NEI)  ➽ more inventions...


Intellectual Property:
U.S. Pat: 9,962,897 issued 2017-04-17

Publications:
N. Carter et al. Mice lacking endogenous IL-10-producing regulatory B cells develop exacerbated disease and present with an increased frequency of Th1/Th17 but a decrease in regulatory T cells.  PMID 21464089
Q. Ding et al. Regulatory B cells are identified by expression of TIM-1 and can be induced through TIM-1 ligation to promote tolerance in mice. PMID 21821911

Collaboration Opportunity:

Licensing and research collaboration


Licensing Contact:
John Hewes, Ph.D.
Email: John.Hewes@nih.gov
Phone: 240-276-5515

OTT Reference No: E-036-2012
Updated: Apr 23, 2018