MD B5: Molecular characterization of the pre-autoimmune effects of Western diet in healthy mice
The objective of the research project is to comprehend the intricate connection between nutrition and autoimmune diseases. Considering the global increase in autoimmune diseases, it is crucial to investigate the role of nutrition in this context. Approximately 5% of the world's population suffers from autoimmune diseases, which are difficult to treat and cause a significant burden on both patients and the economy. This project focuses on the comparison between Western diet, which is characterised by high levels of processed foods, sugars and unhealthy fats, with normal chow diet, calorie-reduced chow diet and calorie-reduced Western diet. My project will examine the effects of these diets at both the cellular and molecular levels in different target organs. For this purpose, serum, adipose tissue, and liver samples from mice exposed to different diets are intensively investigated. To detect minor changes in the inflammatory milieu, precise analyses of inflammatory markers such as CRP, TNF-α and IL-6 are conducted in the serum. In tissue samples, the focus is on the detailed characterization of immune cell populations. In the liver, we additionally plan a comprehensive histological analysis, especially with a focus on steatosis, ballooning, and inflammatory processes. The main objective of my research project is to identify and characterize biomolecular markers that are associated with very early changes in autoimmune diseases. This could lead to a breakthrough, which will allow for not only subtle early detection, but also targeted prevention strategies for individual patients. Additionally, this study provides fundamental insights into the complex interactions between the different diets and the immune system, which could ultimately have significant implications for public health.

- Projects
- 1st Generation
- A: Defining Autoimmune Pre-Disease
- B: Targeting of Autoimmune Pre-Disease
- Associated projects
- Medical doctoral researcher projects
- Concluded projects
- Doctoral researchers
- Medical doctoral researchers
- MD A1: Investigation of the influence of specific CDK inhibitors on neutrophil activation
- MD A2: Anatomical expression of target antigens in autoimmune blistering dermatoses as markers for lesion formation
- MD A3: Structural characterization of skin-directed autoantibodies and their interaction with the antigen to gain insights into autoimmune pre-disease
- MD A4: Do interactions between AT1R autoantibodies derived from patients with systemic sclerosis and endothelial cells lead to endothelial dysfunction?
- MD A5: Establishing a human 3D skin model for pemphigus vulgaris
- MD A6: Assessing vasculopathy in systemic sclerosis using optical coherence tomography
- MD A7: Identification of autoantibodies contributing to the break of immunotolerance in immunization induced mucous membrane pemphigus mouse model
- MD A8: Impact of angiotensin II type 1 receptor antibodies on endothelial dysfunction in systemic sclerosis
- MD A9: Impact of glycosylation on IgG4-induced signaling in neutrophils
- MD A10: Testing a new single chain variable fragment for pemphigus foliaceus in the human skin organ culture model
- MD A11: Impact of glycosylation on IgG3-induced signaling in neutrophiles
- MD A12: Screening for inhibitors to prevent keratinocyte dissociation
- MD A13: Investigation of the local and systemic complement activation in bullous pemphigoid patients
- MD A14: Impact of different IgG subclasses and glycosylation patterns on immune complex-induced signaling in neutrophils
- MD A15: Novel target antigens of the lower basal membrane zone as inducers of autoimmunity of bullous autoimmune dermatoses
- MD A16: Identification of the major epitope of the BP180 ectodomain recognized by serum IgA autoantibodies of patients with pemphigoid diseases – IgA autoantibodies as prognostic marker?
- MD A17: Autoantibody-mediated effects on endothelial and immune cell signaling in systemic sclerosis
- MD A18: Molecular and cellular characterization of pre-autoimmune effects induced by aging in mice
- MD A19: Immunogenic effects of Staphylococcus aureus toxins in autoimmune vasculitis
- MD B1: Testing the effect of kinase inhibitors in the human skin organ culture model for pemphigus vulgaris
- MD B2: Investigation of cigarette smoking-induced autoantibodies against human airway epithelial cells in patients with chronic obstructive lung disease
- MD B3: Contribution of taurine, pyridoxine and pantothenic acid to the pathomechanism of pemphigus vulgaris
- MD B4: The influence of prednisolone treatment on split formation in the human skin organ culture model for pemphigus vulgaris
- MD B5: Molecular characterization of the pre-autoimmune effects of Western diet in healthy mice
- MD B6: Testing established MAP kinase inhibitors in a different approach of the human skin organ culture model for pemphigus vulgaris
- MD B7: Testing the effect of kinase inhibitors in the human skin organ culture model for pemphigus foliaceus
- Ass. doctoral researchers
- Ass. medical doctoral researchers
- 2nd Generation
- 1st Generation