SYNMAT FOR ORGANOIDS · High-throughput and reproducible development of intestinal organoids by microfluidics encapsulation in synthetic niches for intestinal bowel disease research
„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“
- Период
- 2022-07-01 → 2025-09-30
- Финансиране от ЕС
- 257 561 €
- Участници
- 2
- Схема
- MSCA-IF
Линиите свързват координатора с партньорите.
Накратко на български
Синтетични микрогелове ще бъдат използвани за капсулиране на мезенхимални клетки от човешки чревни органоиди. Това помага за разработването на методи за възстановяване на тъканите при пациенти с възпалителни заболявания на червата.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
High-throughput and reproducible development of intestinal organoids by microfluidics encapsulation in synthetic niches for intestinal bowel disease research
Inflammatory bowel disease (IBD), encompassing Crohn’s disease and ulcerative colitis, represents a major and growing global health challenge. Current treatments primarily target inflammation and symptom management but rarely address the underlying tissue damage or support long-term mucosal healing. Consequently, many patients experience recurrent disease flares, progressive tissue degeneration, and serious complications, leading to a diminished quality of life. Moreover, conventional therapies often cause systemic side effects and may lose efficacy over time. The absence of effective regenerative strategies highlights a crucial gap in IBD management. There is an urgent need for innovative therapeutic approaches that not only control inflammation but also actively promote intestinal tissue repair and regeneration. Given the chronic nature of IBD and its increasing prevalence worldwide, developing regenerative solutions would significantly alleviate patient suffering, enhance long-term disease remission, and reduce the economic burden. This project aims to develop an innovative regenerative medicine approach for IBD through the encapsulation of intestinal mesenchymal cells (IMCs) derived from human intestinal organoids within fully synthetic degradable microgels. These engineered systems will provide a cell-instructive environment that supports IMC viability and regenerative function, offering a clinically translatable alternative to animal-derived matrices such as Matrigel. Specific Objectives 1. Engineering of Degradable Synthetic Microgels. 2. Encapsulation and Functional Support of Intestinal Mesenchymal Cells. 3. Evaluation of Regenerative Capacity Using Human Intestinal Organoids. Conclusions: This project will establish a novel regenerative therapy that goes beyond conventional anti-inflammatory treatments by addressing the root cause of intestinal damage in IBD. Through the integration of synthetic biomaterials and patient-derived cells, the proposed system aims to restore intestinal structure and function by combining material engineering, stem cell biology, and organoid technology. This research will provide a versatile and clinically relevant platform for personalized regenerative medicine in IBD. Ultimately, the outcomes are expected to pave the way for next-generation injectable therapies that promote durable mucosal healing and improve the long-term quality of life of patients suffering from chronic intestinal inflammation.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
Intestinal bowel disease (IBD) is a chronic immune-mediated disorder characterized by a complex spectrum of multifactorial disorders, which affects 2.5-4 million people in Europe with a total annual healthcare cost of €4.6-5.6 billion. The unknown aetiology of IBD, along with its heterogeneous and multifactorial nature, make essential the development of novel disease model platforms that enable the fundamental understanding of the disorder. My project aims to develop the next generation of human intestinal organoids (HIOs) in reproducible and high-throughput fashion by microfluidics encapsulation in synthetic niches. This scalable technology will provide a well-controlled mass production of HIOs for disease modelling, drug screening of novel therapeutic targets, and regenerative medicine applications, filling the translational gap with organoids research. I will co-culture HIOs with immune cells and microbiota to obtain native physiological similarities and to develop the next generation of HIOs, which can effectively recapitulate the complex multifactorial spectrum of IBD and allow the identification of new insights into the pathophysiology of the disorder. MSCA Fellowship will provide me with a unique opportunity to exploit my diverse skill set and take fully advantage of available facilities and partnerships of Prof. Andrés García and Prof. Abhay Pandit, who are uniquely positioned to maximize the output of this project and benefit my future career. I will be trained in both discipline-specific and complementary technical training and generic and complementary transferable skills training through an inter-sectoral secondment on a CÚRAM’s industrial partnership to translate this innovative therapeutic technology to the clinic. The disruptive technology developed through this proposal will represent a step change in our understanding of intestinal disorders and advanced therapies, entailing a great contribution to the European knowledge-based economy and society.
Оригинален текст от CORDIS (на английски).
Участници
- UNIVERSITY OF GALWAY · GalwayКоординаторИрландия
- GEORGIA TECH RESEARCH CORPORATION · Atlanta GaСъединени щати
Връзки
- Виж в CORDIS
- DOI: 10.3030/101028216
- https://curamdevices.ie/curam/news-and-events/press-releases/articles/2024/may/researchers-publish-first-computational-insights-into-colonic-motility-to-aid-understanding-of-ulcerative-colitis.html
Данни: CORDIS, © Европейски съюз
