Your browser doesn't support javascript. This means that the content or functionality of our website will be limited or unavailable. If you need more information about Vinnova, please contact us.

Our e-services for applications, projects and assessments close on Thursday 19 September at 4:30pm because of system upgrades. We expect to open them again on Friday 20 September at 8am the latest.

Development of a novel and unique disease-specific treatment for ANCA vasculitis

Reference number
Coordinator Toleranzia AB
Funding from Vinnova SEK 2 912 709
Project duration April 2023 - March 2025
Status Ongoing
Venture Swelife and Medtech4Health - Collaborative Projects for Improved Health
Call Swelife and Medtech4Health - Collaborative projects for better health autumn 2022

Purpose and goal

TOL3 is a drug candidate for ANCA vasculitis, an autoimmune disease lacking safe and effective therapies. The goal is to develop an improved TOL3 through an innovative approach consisting of identifying the specific epitopes that ANCA vasculitis patients present and react to and designing a novel TOL3 that contains multiple disease-specific epitopes comprising the peptides identified. This version of TOL3 is considered to have potential to induce immunological tolerance providing long-lasting or curative effect across an immunologically heterogenous patient population.

Expected effects and result

A successful project may result in two highly innovative outcomes: i) a new, improved TOL3, which will be the first disease-specific treatment with potential to provide long-term remission or even cure of ANCA vasculitis, and ii) a completely new technology platform for design of novel drugs for autoimmune diseases.

Planned approach and implementation

MHC-II MPO epitopes that ANCA vasculitis patients present and respond to will be identified in a Swedish cohort of patients by an advanced LC-MS approach. These will be used to design and recombinantly produce an improved TOL3 containing multiple disease-specific epitopes, potentially inducing tolerance in a majority of patients with different genetic backgrounds. The immunogenicity risk will be assessed by in silico screening, and the new version of TOL3 will be evaluated in an animal model of ANCA vasculitis.

External links

The project description has been provided by the project members themselves and the text has not been looked at by our editors.

Last updated 26 May 2023

Reference number 2022-03433