About the VHIR
Here at the Vall d'Hebron Research Institute (VHIR) we promote biomedical research, innovation and teaching. Over 1,800 people are seeking to understand diseases today so the treatment can be improved tomorrow.
Research
We are working to understand diseases, to find out how they operate and to create better treatments for patients. Get to know about our groups and their lines of research.
People
People are the centre of the Vall d'Hebron Research Institute (VHIR). This is why we are bound by the principles of freedom of research, gender equality and professional attitudes that HRS4R promotes.
Clinical trials
Our work is not just basic or translational; we are leaders in clinical research. Enter and find about the clinical trials we are conducting and why we are a world reference in this field.
Progress
Our aim is to make the research carried out at the Vall d’Hebron Research Institute (VHIR) a driving force for transformation. How? By identifying new channels and solutions for the promotion of people's health and well-being.
Core facilities
We offer specialist support for researchers, internal and external alike, ranging from specific services to preparing complete projects. All this, from a perspective of quality and speed of response.
News
We offer you a gateway for staying up to date on everything going on at the Vall d’Hebron Research Institute (VHIR), from the latest news to future solidarity activities and initiatives that we are organising.
Speaker: Dr. Cristina Solé Marce, Main researcher, Rheumatology (VHIR)
Systemic lupus erythematosus (SLE) is a chronic inflammatory autoimmune disease with a wide range of manifestations and organ involvement. Lupus nephritis (LN) occurs in 40-75% of SLE patients and is associated with an unpredictable course. Despite conventional therapy, LN is still one of the main causes of short- and long-term morbidity and mortality, with up to 30% of patients progressing to chronic renal failure. There is a need to find new, more effective, selective and targeted treatments. In this sense, the new chemical antigen receptor (CAR) technology that depletes B cells has proven to be a good possible alternative and the first clinical trials have already begun. In our group, we have studied a variant of this technology, the chimeric autoantigen receptor T-receptor therapy (CAAR-T) that selectively depletes anticoagulant B cells using the NZBWF1/J spontaneous lupus murine model. At the same time, we are also interested in the use of nanotechnology to encapsulate immunosuppressive drugs and selectively target them to the rontium. In this seminar, the results of these two research projects will be presented.
Host: eCORE AVANT (VHIR)