Technology ID
TAB-4403

Novel Chemoattractant-Based Toxins To Improve Vaccine Immune Responses for Cancer and Infectious Diseases

E-Numbers
E-027-2005-0
Lead Inventor
Arya, Bira (NIA)
Co-Inventors
Matsushima, Kouji (University of Tokyo)
Bataar, Dolgor (NIA)
Applications
Therapeutics
Therapeutic Areas
Oncology
Immunology
Development Stages
Discovery
Lead IC
NIA
ICs
NIA

Cancer is one of the leading causes of death in United States and it is estimated that there will be more than half a million deaths caused by cancer in 2009.  A major drawback of the current chemotherapy-based therapeutics is the cytotoxic side-effects associated with them.  Thus there is a dire need to develop new therapeutic strategies with fewer side-effects.  Immunotherapy has taken a lead among the new therapeutic approaches.  Enhancing the innate immune response of an individual has been a key approach for the treatment against different diseases such as cancer and infectious diseases.

This technology involves the generation of novel chemoattractant toxins that deplete the T regulatory cells (Treg) or other immunosuppressive or hyperactivated cells locally.  Treg controls activation of immune responses by suppressing the induction of adaptive immune responses, particularly T cell responses.  Immunosuppressive cells such as tumor infiltrating macrophages, regulatory T cells, regulatory B cells, or NKT and other cells down regulate antitumor immune responses.  The chemoattractant toxins consist of a toxin moiety fused with a chemokine receptor ligand, such as chemokines and various chemoattractants, that enables specific targeting and delivery to the regulatory cells. This technology is advantageous over the more harmful antibodies and chemicals that are currently used for the systemic depletion of regulatory cells.  The current technology can be used therapeutically in a variety of ways.  They can be used together with vaccines to increase efficacy of the vaccine for the treatment of cancer, and can be used to locally deplete Treg, Bregs, or other immuno suppressive cells to induce cytolytic cell responses at the tumor site or to eliminate chronic infectious diseases such as HIV and tuberculosis.

Development Status: 
The technology is currently in the pre-clinical stage of development.
 

Competitive Advantages:

Commercial Applications:

  • New chemoattractant-based toxins targeted towards Treg cells.
  • New chemoattractant-based toxins targeted towards immunosuppressive B cells, NKT and macrophages.
  • New chemoattractant based toxins targeted towards local depletion of hyperactivated CD4 T cells to treat autoimmune diseases.
  • Chemoattractant-based toxins depleting Treg cells or other immunosuppressive cells causing enhanced vaccine immune responses.
  • Novel immunotherapy by increasing vaccine efficacy against cancer and infectious diseases.
Licensing Contact:
Guyton, Nicole
darackn@mail.nih.gov