CORDIS · ERYSO
Engineered erythrocytes and erythrocyte extracellular vesicles for advanced Photodynamic and Sonodynamic therapy
- Code
ERYSO- Programme
- HORIZON
- Call
HORIZON-MSCA-2025-SE-01-01- Status
- SIGNED
- Period
- 2027-01-01 – 2030-12-31
Official data · CORDIS · synced 2026-10-18 03:29 · official record
Participants
| Organisations | Role | Country | Grant |
|---|---|---|---|
| ASOCIACION CENTRO DE INVESTIGACION COOPERATIVA EN BIOMATERIALES- CIC biomaGUNE | coordinator | ES | 946 890 € |
| UNIVERSITA DEGLI STUDI DI ROMA TOR VERGATA | participant | IT | 340 680 € |
| FRIEDRICH-ALEXANDER-UNIVERSITAET ERLANGEN-NUERNBERG | participant | DE | 110 220 € |
| MAIBE SRL | participant | IT | 100 200 € |
| DANUBE PRIVATE UNIVERSITY GMBH | participant | AT | 100 200 € |
| TECHNION - ISRAEL INSTITUTE OF TECHNOLOGY | participant | IL | 100 200 € |
| ТРАКИЙСКИ УНИВЕРСИТЕТ | participant | BG | 90 180 € |
| Prove Innomed Company Limited | associated partner | TH | |
| YAYASAN PERGURUAN TINGGI KRISTEN PETRA | associated partner | ID | |
| UNIVERSITY OF MAURITIUS | associated partner | MU | |
| UNIVERSIDAD NACIONAL DEL SUR | associated partner | AR | |
| MAHIDOL UNIVERSITY | associated partner | TH | |
| CHULALONGKORN UNIVERSITY | associated partner | TH | |
| UNIVERSIDAD DE BUENOS AIRES | associated partner | AR |
Description
ERYSO aims to develop innovative therapeutic solutions based on photodynamic (PDT), and sonodynamic (SDT) therapies usingengineered red blood cells (RBCs) and extracellular vesicles (EVs) derived from RBCs in combination with magnetothermal (MHT)therapy. Both RBCs and RBC-derived EVs are characterized by their ability to transport hemoglobin, the body's natural oxygen carrier,and exhibit long circulation times, providing a unique advantage for therapeutic delivery. Encapsulating photosensitizers (PSs) andengineering these carriers for tumor targeting addresses a major limitation of existing PDT and SDT solutions, hypoxic tumor regions, by delivering oxygen directly to these areas, enhancing therapy efficacy. Combining PDT and SDT with MHT further amplifiestherapeutic outcomes, providing a multimodal approach to tumor eradication.Magnetic nanoparticles for MHT or titanium oxide nanoparticles for SDT will be encapsulated in the carriers to enable combination oftherapies. Tumor targeting will be achieved by functionalizing RBC glycocalyx with targeting peptides or incorporating functionalizedlipids into EVs. Enhanced tumor uptake of EVs and RBCs will be facilitated through the Focus Ultrasound (FUS) technique, whichtemporarily permeabilizes the blood-tumor barrier. Tumor targeting and oxygen delivery will be monitored using advancedmolecular imaging techniques such as Positron Emission Tomography (PET) and Single Photon Emission Computed Tomography(SPECT). Therapeutic efficacy will be evaluated in relevant tumor models, combining molecular imaging and histopathologicalanalysis.The project envisions developing personalized therapies based on autologous patient components, ensuring localized treatmentwith reduced side effects. By leveraging the natural compatibility of RBCs and EVs and integrating cutting-edge targeting and deliverytechnologies, ERYSO advances the potential of personalized and multimodal cancer therapies.
Official data · CORDIS · synced 2026-10-18 03:29 · official record · Licence: © European Union, CC BY 4.0 (Commission reuse policy).