TP A2: Identification of novel B cell inhibitory compounds
Controlling antibody production by B cell derived plasma cells is one approach for the treatment of autoimmune disorders. However, systemic use of corticosteroids has been still the mainstream of the therapy despite the potential severe adverse effects. In addition, newer treatments including monoclonal antibodies against CD20 expressing B cells, e.g. Rituximab©, are not universally applicable, most likely due to high cost, long-term efficacy and safety.
Based on these considerations, my PhD project aims to identify immunomodulatory agents that affect B cell function. For this purpose the effect of the compounds on B cell proliferation and immunoglobulin (Ig) production will be investigated.
- 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