Genetically Engineered Treg Cell Therapy for Immune Disorders

Description:

Adoptive Cell Therapies for Chronic Inflammatory and Autoimmune Disorders
Chronic inflammatory and autoimmune disorders affect over 3% of the US population with no treatment options available that sustainably reverses symptoms or cures patients. Adoptive Treg cell therapies are promising treatment options due to their ability to persistently induce tissue homeostasis – effectively reversing the effects of autoimmune and chronic inflammatory disorders. However, efficacy of adoptive Treg therapies are limited by (1) Tregs switching to pro-inflammatory CD4 T-cells (CD4Tconv cells) ex-vivo and in-vivo, and (2) low functional Treg abundance in patient source material.


Innovation: IL37 Overexpressing T-cells
Genetically engineering CD4 T-cells to overexpress IL-37 stabilizes a Treg phenotype for the purpose of adoptive cell therapy for chronic inflammatory and autoimmune diseases (IL37 OE T-cells). Futhermore, IL37 OE T-cells maintain high expansion and suppression properties ex-vivo and in-vivo – thereby (1) preventing Tregs from switching to CD4 Tconv-cells and (2) increasing the source material options for adoptive T-cell therapy. IL-37 OE T-cell therapy has yielded beneficial results in pre-clinical mouse models of psoriasis, traumatic brain injury, and GvHD.


Advantages:
•IL37 OE Tregs display improved expansion and suppressive function ex-vivo.

 

Download Summary Document Here:

https://cuamc.technologypublisher.com/files/sites/cu5974h_translation_application_for_il37_tregs_ncs_2023_.pdf

Category:
Therapeutics
For Information, Contact:
Doreen Molk
University of Colorado
doreen.molk@cuanschutz.edu
Inventors:
Mayumi Fujita
Douglas Osborne
Maki Nakayama
Disease Areas:
Regenerative Medicine
For inquiries, email: cuinnovations@cuanschutz.edu.     © 2024. All Rights Reserved. Powered by Inteum