Ass. TP A1: Unravel principles of the biomolecular network in pemphigus vulgaris
Pemphigus comprises a group of autoimmune diseases targeting either desmoglein 3 (Dsg3) or Dsg1/3 in Pemphigus vulgaris (PV). They can be found on epidermal and hair follicle stem and progenitor cells as well as mucous membranes. Autoantibodies targeting these proteins lead to disruption of cell-cell adhesion and ultimately to blister formation on the skin and mucous membranes. In this project, PV should be used as a model to establish a comprehensive and integrative biophysical and biochemical Dsg3 network to define the clinically relevant, transcellular tissue communication code driving tissue remodelling during injury. To achieve this goal, in this project, the human PV organ culture will be used.
- Projects
- 1st Generation
- A: Defining Autoimmune Pre-Disease
- B: Targeting of Autoimmune Pre-Disease
- Associated projects
- Ass. TP A1 - Unravel principles of the biomolecular network in pemphigus vulgaris
- Ass. TP A2: Unravel Principles of Self-Organization in Injured Tissue
- Ass.TP A3 - Landscape of the kinome of several organs of mice of different ages and sexes
- Ass. TP A4 - Complement C3 as key driver of pemphigoid disease pathogenesis
- Ass. TP. A5 - Crosstalk between T cells and B cells in the differentiation of pathogenic plasma cells in pemphigoid diseases
- Ass. TP A6 - Skin-infiltrating T and B cells in the pathogenesis of pemphigoid diseases
- Ass. TP A7- Stromal regulation of inflammation in pemphigoid diseases
- Ass. TP A8 - The role of neutrophils in the regulation of the adaptive immunity in pemphigoid diseases
- Ass.TP B1 - Kinase cascades in neutrophils as therapeutic target in pemphigoid disease
- MD projects
- Concluded Projects
- 2nd Generation
- 1st Generation
Doctoral Candidate
Principal investigators
Mentor
Antje Müller