Archives: “Biological & Mechanistic”

Showing 141 - 150 of 241 posts

Copper Transporter SLC31A1 in Th17 Cells and Multiple Sclerosis

https://www.coltonconsortium.org/projects/copper-transporter-slc31a1-in-th17-cells-and-multiple-sclerosis/

Investigating how copper transport via SLC31A1 regulates pro-inflammatory Th17 cell activity, this project uncovers a novel link between immune cell metabolism and MS, pointing toward new therapeutic targets.

Targeting Allograft Inflammation with CAR Tregs in Transplantation

https://www.coltonconsortium.org/projects/targeting-allograft-inflammation-with-car-tregs-in-transplantation/

Engineering HLA-DQ–specific CAR Tregs to selectively suppress anti-donor immune responses at sites of graft inflammation, this project seeks a more precise, durable alternative to broad immunosuppression in transplantation.

Colton Center for RNA Exploration in Autoimmune Therapeutics (CREATE)

https://www.coltonconsortium.org/projects/colton-center-for-rna-exploration-in-autoimmune-therapeutics-create/

Developing next-generation mRNA-LNP therapeutics that selectively modulate or deplete pathogenic immune cells to treat type 1 diabetes, lupus, multiple sclerosis, and other severe autoimmune conditions.

A Novel Skin-Based Approach to Treat Lupus Nephritis

https://www.coltonconsortium.org/projects/a-novel-skin-based-approach-to-treat-lupus-nephritis/

Repurposing topical MC903, an FDA-approved vitamin D analog, to trigger skin-derived bile acid synthesis and generate systemic anti-inflammatory effects in lupus nephritis.

Autoantibodies in Long COVID

https://www.coltonconsortium.org/projects/autoantibodies-in-long-covid/

Investigating the autoimmune and immune dysregulation mechanisms underlying Long COVID to improve diagnosis, treatment, and biological understanding of persistent symptoms.