Technology Details

Designing universal donor B cells that will respond to antigen independently of T cell boost

  • Stage: Preclinical in vitro 
  • Type: Therapeutic
  • Categories: HSC Therapy; Hybridoma / Antibody; Immuno Oncology

Technology Overview

Vaccines increase immunity against infections by stimulating B cells to produce antibodies against the infectious agent. In addition to infections, antibodies are also useful as treatment for different autoimmune conditions, and cancer. To mount a potent B cell response, interaction between CD40 (expressed on the surface of B cells) and CD40 ligand (CD40L; expressed on the surface of CD4+ T cells) is typically required for expansion, survival and differentiation of the B cells. B cell dependence on T cell interaction via MHC presentation also limits development of universal donor B cells for broader therapeutic applicability. To overcome this, Fred Hutchinson Cancer Center researchers have developed a method to genetically modify B cells to express fusion proteins that link extracellular antigen binding domains to CD40 signaling domain. This allows CD40 signaling activation upon antigen binding, independently of interaction with CD40L on T cells. Two approaches to link CD40 signaling to antigen binding have been developed: (a) Linking CD40 signaling to B cell receptor (BCR) signaling and (b) Linking CD40 signaling domain to engineered extracellular antigen binding domains.

Applications

  •      Enhancing responses of B cells engineered to combat common respiratory viruses (e.g., RSV, HMPV, influenza, etc.)  
  •      Enhancing responses of B cells engineered to combat other viral (e.g., HIV, CMV, EBV, hepatitis C, herpes simplex, etc.) or bacterial (e.g., Bordetella, clostridium difficile, etc.) infections  
  •      Potentiating therapeutic response of B cells producing antibodies for autoimmune diseases and cancer  

Advantages

  •      Improves response activity of B cells independent of CD40L interaction and thus leads to a greater response to a vaccine or treatment
  •      Obviates the need for MHC II interaction between T cell and B cell (either by surpassing CD40 – CD40L interaction, or by a genetically engineered deletion of MHC II molecules in B cells) allowing for ‘universal’ donor B cell therapeutics   

Patent Information

  • WO/2022/170271 A2

Market Overview

  • Given the broad applicability of the technology, the market potential is promising. The global respiratory virus infection drugs market is expected to exceed a value of US$ 82.8 billion by 2030. Even though the therapeutic modalities are fragmented, the global autoimmune disease therapeutics market was worth $ 54.8 B (USD) in 2021 and expected to grow at a CAGR of 12.9%. Similarly, the global HIV therapeutics market is expected to surpass $ 40.3 B (USD) by 2030.

Investigator Overview

  • Justin Taylor Ph.D.; Associate Professor - Vaccine and Infectious Disease Division
Tech ID: 20-143