TP12: S100A8 and S100A9 proteins as therapeutical targets in experimental bullous pemphigoid
Bullous pemphigoid (BP) represents a severe autoimmune bullous disease associated with autoantibodies to hemidesmosomal proteins. A novel and innovative therapy could be the blockade of the proinflammatory proteins S100A8/A9, which have been shown to be involved in several chronic inflammatory processes like rheumatoid arthritis or Crohns disease.
S100A8/A9 is highly upregulated in lesional skin of experimental BP. By using S100A8/A9-deficient mice as well as immunological and pharmalogical inhibitors of S100 proteins and their receptors we will analyse (i) the principal role of S100A8/A9 in the pathogenesis of BP and (ii) their potential as therapeutical targets in the disease.
He received his Dr. rer. nat degree in 02/2015 and now works as a PostDoc in the AG Ludwig at the Lübecker Institute of experimental Dermatology (LIED).
- Projects
- Projects
- Associated projects
- MD projects
- Associated MD projects
- Concluded projects
- Concluded TP
- TP1 - Modulation of isotypes
- TP2 - Targeted fusion proteins
- TP3 - Selective FcRn inhibition
- TP4 - IL-35, Treg and EAE
- TP5 - Apoptotic cells
- TP6 - Mast cell / T cell interactions
- TP7 - Fc gamma receptors
- TP8 - IgG- and C-receptors
- TP9 - IVIG
- TP10 - HMGB1 Protein
- TP11 - IL15 / IL15Rα
- TP12 - S100 proteins
- TP13 - Treatment-refractory B cells
- TP A1 - Treatment strategies
- TP A2 - B cell inhibition
- TP A3 - IL-17 in EBA
- TP A4 - The pathophysiological role of Th17cells in Bullous pemphigoid
- TP A5 - C5a/C5aR
- TP A6 - Signals leading to glycosylated antibodies
- TP A7 - IL-16 & MIF in autoimmunity
- TP B1 - B cell transcriptome
- TP B2 - Antigen-specific T cells
- TP B3 - Metabolomics
- TP B4 - Resident plasma cells
- TP B5 - Anti-CD37 antibodies
- TP B6 - Systemic Sclerosis
- Concluded Ass.TP
- Concluded MD TP
- Concluded Ass. MD TP
- Concluded TP