Immune Monitoring for RIsk STratification in Solid Organ Transplant Recipients

Informations projet

ImMoRiSt

N° de convention de subvention: 710079

DOI

10.3030/710079

Projet clôturé

Date de signature de la CE 11 Decembre 2015

Date de début 1 Février 2016

Date de fin 31 Juillet 2016

Financé au titre de

• SOCIETAL CHALLENGES - Health, demographic change and well-being

Coût total

€ 71 429,00

Contribution de l’UE

€ 50 000,00

Coordonné par

LOPHIUS BIOSCIENCES GMBH
Germany

Periodic Reporting for period 1 - ImMoRiSt (Immune Monitoring for RIsk STratification in Solid Organ Transplant Recipients)

Période du rapport: 2016-02-01 au 2016-07-31

Résumé du contexte et des objectifs généraux du projet

Every year ~ 40.000 patients throughout the EU are transplanted with a solid organ e.g. kidney, lung, liver, heart or receive a stem cell transplantation (SCT). Adequate and personalized treatment of the severe and in part life threatening clinical complications is impeded by the lack of appropriate diagnostic tests that help physicians to ascertain the exact dosage of immunosuppressive drugs and identify patients an increased risk for transplantation related complications. This is mandatory to avoid organ rejection and to diminish clinical complications caused by infections.

Lophius Biosciences GmbH has developed innovative immune monitoring tools, the so called “I-Scan” products providing important information on the strength and functional impairment of the cellular immune system in all groups of transplant (solid organ and stem cell) recipients within 24 h. The “I-Scans” diagnostics combine proprietary stimulants (either T activated® antigens of pathogens (applied in T-Track® CMV) or a cocktail of cell-type specific stimulants (T-Track® ImmunoScan)) with a highly sensitive readout method (IFN- ELISpot).

Travail effectué depuis le début du projet jusqu’à la fin de la période considérée dans le rapport et principaux résultats atteints jusqu’à présent

Both assay formats are based on Lophius’ proprietary “T-activation® technology” enabling a highly sensitive qualitative and quantitative measurement of cell-mediated immune function. The feasibility study performed during Phase 1 explored both, the clinical biomarker validation study and the best market entry strategy for two variant immune monitoring tools – the T-Track® CMV and the T-Track® ImmunoScan.

Progrès au-delà de l’état des connaissances et impact potentiel prévu (y compris l’impact socio-économique et les conséquences sociétales plus larges du projet jusqu’à présent)

A key outcome of the ImMoRiSt feasibility study was that stem cell transplantation (SCT) is the therapeutic area better suited as SOT to clinically validate and commercialize Lophius’ I-Scan IVD tests. Together with the study partners identified during the feasibility study Lophius will submit a Phase 2 application in the topic SMEInst-05-2016-2017: supporting innovative SMEs in the healthcare biotechnology sector, that includes the challenge “Clinical research for the validation of biomarkers and/or diagnostic medical devices”.

The clinical validation of a selected I-Scan product which is planned for Phase two of this innovation project will demonstrate that functional immune monitoring of a network of clinically relevant effector cells of the innate and adaptive immune system will substantially improve the outcome and aftercare of SCT recipients.

Main Contractor