REDOXIT · Reactive oxygen species (ROS) as Elixirs against chronic Disease: OXidative regulatory mechanisms In T cells and neutrophils.
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2015-07-01 → 2019-06-30
- EU contribution
- €144,000
- Participants
- 4
- Scheme
- MSCA-RISE
Lines connect the coordinator with its partners.
Results in brief
Reactive oxygen species (ROS) as Elixirs against chronic Disease: OXidative regulatory mechanisms In T cells and neutrophils.
REDOXIT 2015-2019 https://www.surrey.ac.uk/redoxit Within our four-year programme of knowledge transfer and networking between University of Surrey (SURREY, UK), Aston University (ASTON, UK), Erlangen Universitat (FAU, Germany) and Redoxis AB (Redoxis, Sweden), we have targeted an emerging area of biology; the role of reactive oxygen species (ROS) in the regulation of immune responses and age-associated inflammatory conditions; we applied small molecule candidate drugs to generate ROS and used innovative approaches for biomarker identification in models of chronic immune disease. This research has significant potential for application in human health and is of particular relevance to the ageing population. The number of people in the European workforce aged between 55-64 will increase by one third in the next 20 years, growing from 15% to 20%. The number of work days lost by people in this age with rheumatoid arthritis alone represents 20% of all absences. It is therefore important to identify cost-effective treatments that improve the well-being of older people with chronic inflammatory disease and to enable their continued participation in working economy. Our goal was to develop new compounds, explore their potency and protect emerging IP, to grow the economic position of the SME and develop researchers. The knowledge economy is one of Europe's leading strengths. To grow this capability we need to promote the exchange of ideas. Through the RISE scheme we have successfully delivered training, knowledge transfer and skills exchange between partners and early career researchers. The challenges that we are addressed were balanced between industrial application and basic science, with a focus on knowledge transfer and drug re-purposing. We conclude that; 1. Novel NOX2 activators are potent inflammatory modulators in primary immune cells. 2. Novel NOX2 activators are effective in disease management in animal models of autoimmune disease. 3. The downstream pathways of NOX2 activator effects on T cells predominantly feature calcium channels. 4. ROS regulate T cell- and neutrophil inflammatory activity. 5. A strengthened academic-industrial relationship has been achieved that has led to a further collaborative project starting in 2020, NeutroCure, that will develop and apply a new class of ROS generators for chronic autoimmune disease. Early career researcher skills have been advanced through embedding new skills, expertise and knowledge transfer in individuals and the collaborator organisations. 6. Innovations have been disseminated within Europe through presentations and worldwide through publications
Data: CORDIS, © European Union
Project objective
We are proposing a four-year programme of knowledge transfer and networking between University of Surrey (SURREY, UK), Aston University (ASTON, UK), Friedrich-Alexander Universitat (UKER, Germany) and Redoxis AB (Redoxis, Sweden). The project targets an emerging area of biology, i.e. reactive oxygen species (ROS)-mediated regulation of immunology and ageing; it brings together the application of small molecule candidate drugs to generate ROS and uses innovative approaches to biomarker identification in models of chronic immune disease. This research has significant potential for application in human health and is of particular relevance to the ageing population.Training, knowledge transfer and skills exchange in this emergent area is important to extend the EU’s reach through cutting edge expertise. Interchange in this way will facilitate and promote early career researcher development into tomorrow’s research leaders. It will encourage new, cross-European collaboration between academia and industry. This tri-partite consortium brings together groups with very complementary expertise for knowledge exchange to benefit early career researchers: ASTON – in the biochemical analyses of ROS; SURREY in thiol oxidation and effects in vitro and ex vivo on and within immune cells relevant for biomarker development in chronic disease; UKER - in animal models of chronic diseases such as systemic lupus erythematosus (SLE) and arthritis; and Redoxis on development of novel drugs that stimulate production of ROS from the NOX2 enzyme as means to modulate chronic inflammation. The project objectives and challenges present a balanced mix between industrial application and basic science, with a focus on knowledge transfer and drug development. Through future collaborative funding, we anticipate far-reaching applications of redox modulators to manage chronic disease and increase the knowledge of both autoimmunity and ageing of the immune system.
Original text from CORDIS.
Participants
- UNIVERSITY OF SURREY · GuildfordCoordinatorUnited Kingdom
- ASTON UNIVERSITY · BirminghamUnited Kingdom
- REDOXIS AB · LundSweden
- UNIVERSITATSKLINIKUM ERLANGEN · ErlangenGermany
Links
- View on CORDIS
- DOI: 10.3030/644035
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5b5739ac1&appId=PPGMS
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5bc90c527&appId=PPGMS
- https://www.ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5c6f692ee&appId=PPGMS
- https://www.surrey.ac.uk/redoxit
Data: CORDIS, © European Union
