Novel engineered cytokines for human therapy
Developing a novel protein design strategy for helix-bundle cytokines to enhance their therapeutic efficacy and safety, aiming to establish a start-up for commercialization.
Projectdetails
Introduction
Cytokines are biomolecules of great potential interest for human therapy. They modulate the immune system and play an important role in cancer, inflammation, immune response, and tissue regeneration. Despite their great potential, there are only a handful of cytokines approved for therapeutic purposes.
Challenges in Cytokine Therapy
This is because many of them can have adverse side effects as they usually target different cell types, which adds to their low serum half-life, high production costs, or lack of physiological efficacy.
Proposed Improvements
Different methods have been proposed to improve the pharmacodynamics and pharmacokinetics of selected cytokines. However, other properties also need improvement, such as:
- Achieving effective local concentration at the target site.
- Promoting the right activity in cytokines with dual functionality.
- Decreasing toxicity by removing binding to unwanted cell types.
New Protein Design Strategy
To help solve these issues, we have developed a new protein design strategy that can be applied to all helix-bundle cytokines, many of which have been shown to be therapeutically relevant. The resulting products are uniquely modified cytokines with improved properties.
Enhanced Properties
Among such properties, our products show:
- Increased stability.
- Higher affinity and specificity for their target receptors.
- Reduced toxicity.
All of these enhancements translate into greater safety and efficacy.
Validation and Future Plans
We have initial evidence both in vitro and in vivo of the superiority of our designs over conventional cytokines. In this project, we will fully validate our technological platform and advance in the development of a business plan following the advice of several venture capital and pharma companies contacted to date, with the idea of laying the basis for the creation of a new start-up company.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 150.000 |
Totale projectbegroting | € 150.000 |
Tijdlijn
Startdatum | 1-7-2022 |
Einddatum | 30-6-2024 |
Subsidiejaar | 2022 |
Partners & Locaties
Projectpartners
- FUNDACIO CENTRE DE REGULACIO GENOMICApenvoerder
Land(en)
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Chemical Engineering of Natural Killer Cells for Cancer Immunotherapy
This project aims to develop a faster, cheaper method for producing chemically engineered immune cells for cancer immunotherapy, comparing it to traditional CAR-NK cell approaches.
Subcutaneous delivery of theranostic cell-based therapies
This project aims to create a biodegradable hydrogel for subcutaneous delivery of simili-CAR NK cells and cytokines to enhance cancer treatment efficacy while reducing IV administration challenges.
Modular Targeted Nanoplatform for Immune Cell Regulation and Therapy
ImmuNovation aims to develop a targeted nano-immunoModulator nanovaccine to enhance antitumor immunity against CEACAM5+ gastrointestinal cancers, offering a safer and more effective treatment alternative.
Developing the next generation of cis-targeting macrophage-T cell cancer immunotherapies
This project aims to develop dual-modulatory agents to enhance anti-tumor immune responses in cancer immunotherapy while minimizing side effects, seeking proof-of-concept validation.
Polyclonal anti-tumor immunity by engineered human T cells
This project aims to enhance adoptive T cell therapies for solid tumors by engineering TCR sensitivity and safety, creating robust, antigen-agnostic immune responses to improve patient outcomes.
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