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
- MD projects
- Concluded Projects
- MDs
- MD A1 - Investigation of the influence of specific CDK inhibitors on neutrophil activation
- MD A2 - Conception of an anatomical expression of landscape 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 - Optimization and exploitation of a 3D model of human skin for translational use
- MD A6- To study vasculopathy in systemic sclerosis
- MD A7- Identification of autoantibodies contributing to the break of immunotolerance in immunization induced MMP mouse model
- MD A8- The role of AT1R antibodies and extracellular vesicles in mediating endothelial dysfunction in systemic sclerosis with pulmonary arterial hypertension
- 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 keratinocytes dissoziation
- MD A13- Investigation of the local and systemic complement activation in bullous pemphigoid
- MD A14 - Impact of different subclasses on immune complex-induced signaling in neutrophils.
- MD A15 - Novel target antigens as inducers of autoimmunity of autoimmune bullous 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 B1 - Testing the effect of kinase inhibitors in the human skin organ culture model
- MD B2 - Cigarette smoking-induced autoantibodies
- MD B3 - Contribution of taurine, hypoxanthine, vitamin B5 and B6 in 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 the effect of kinase inhibitors in the human skin organ culture model for pemphigus foliaceus
- MD B7 - Testing the Effect of Kinase Inhibitors in the Human Skin Organ Culture (HSOC) Model for Pemphigus Foliaceus
- PhDs
- Ass. projects
- Ass MDs
- MDs
- 2nd Generation
- 1st Generation