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Personalised Medicine for Intervertebral Disc Regeneration- Integrating Profiling, Predictive Modelling and Gene Activated Biomaterials

Descripción del proyecto

Un tratamiento personalizado de la lumbalgia

La lumbalgia asociada a la degeneración de los discos intervertebrales (DIV) es un problema de salud creciente en la sociedad moderna. Pese a que se están estudiando diversos biomateriales y tratamientos en ensayos clínicos, los diferentes microentornos de los DIV hacen que sea poco probable que un método universal resulte eficaz para todos los casos. El proyecto financiado con fondos europeos INTEGRATE propone combinar el cribado «in vitro» y el modelado «in silico» para diseñar tratamientos celulares basados en el perfil de DIV individual y predecir los resultados de la regeneración. El proyecto también desarrollará biomateriales activados por genes que tendrán el potencial de regenerar la matriz de DIV y modular los procesos inflamatorios, lo que abrirá nuevas vías para estrategias terapéuticas mínimamente invasivas.

Objetivo

Lower back pain is a global epidemiological and socioeconomic problem. Biomaterial and cell-based therapies have been pursued for the treatment of degenerated intervertebral disc (IVD), with a number of clinical trials underway. However, the degenerated intervertebral disc has a distinct environment (e.g. altered oxygen, glucose, acidity, inflammatory cytokine levels) that is unique to an individual (i.e. patient-specific) and will ultimately determine the likelihood and rate at which regeneration can occur. A “one size fits all” approach will lead to the failure to demonstrate efficacy of advanced therapies, as they are not being designed or personalised for individual patients. This proposal envisions a future whereby advanced gene activated cell therapies are personalised (targeting regeneration or modulating inflammation) to treat back pain based on knowing the individuals unique disc microenvironment. This will be achieved through profiling of individual patient disc microenvironmental factors, with in vitro screening and in silico modelling to design cell therapies and predict regeneration outcomes (Aim 1) combined with the development of tailored functionalised gene activated biomaterials (Aim 2), to enhance matrix formation and modulate the inflammatory processes (Aim 3). Gene-based therapy offers several advantages over direct delivery of proteins or small molecules, among them the possibility of sustained efficacy and endogenous synthesis of growth factors or suppression of inflammatory factors and pathways. The platform technology (personalised gene activated biomaterials to regulate regeneration and inflammation) and knowledge (tailoring cell therapies to suit patient-specific microenvironments) generated through this research are beyond the current state-of-the-art and will provide a significant transformative scientific and clinical step change opening new horizons in minimally-invasive therapeutic strategies.

Régimen de financiación

ERC-COG - Consolidator Grant

Institución de acogida

THE PROVOST, FELLOWS, FOUNDATION SCHOLARS & THE OTHER MEMBERS OF BOARD, OF THE COLLEGE OF THE HOLY & UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN
Aportación neta de la UEn
€ 1 754 543,00
Dirección
COLLEGE GREEN TRINITY COLLEGE
D02 CX56 DUBLIN 2
Irlanda

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Región
Ireland Eastern and Midland Dublin
Tipo de actividad
Higher or Secondary Education Establishments
Enlaces
Coste total
€ 1 754 543,00

Beneficiarios (2)