A7: CD4+ T cell receptor sequences during progression towards experimental pemphigoid
Background. In mouse models of pemphigoid, presence of autoantibodies at the dermal-epidermal junction is not sufficient to induce pathology (J Immunol 187:5043, J Invest Dermatol 140:1713). Moreover, our data demonstrated that PD pathogenesis correlates with IFN gamma-producing Th1 cells, whereas IL-4-producing Th2 or IL-10-producing Tregs suppress disease manifestation. Because lineage decision of CD4+ T cell differentiation is controlled by the T cell receptor (TCR) signaling strength, we hypothesize that T cell subsets emerge from distinct T cell clones, which compete with each other for survival and number of progenies. Eventually, during the transition from symptomless autoimmunity to autoimmune disease, Th1 cells become superior and accumulate over time. Our preliminary data revealed that the clinical manifestation of PD correlates with shifts in the V-J gene usage of the TCR-Beta chains (J Invest Dermatol. in press, PMID: 32057838, Fig. A7-1).
Objective. (i) Characterize the disease-specific TCR sequences and transcriptomes of CD4 subsets, (ii) explore disease-specific changes in the Th1, Th2 and Treg compartments in PD mouse models, and (iii) identify factors that modulate the ratio of disease-associated T cell clones.
Work program. Together with A9, compare the TCR-Beta sequences and transcriptomes of draining lymph nodes and skin lesions from healthy with those from pre-diseased and diseased mice. FACS will be used to define T cell subsets using surface markers, transcription factors and cytokines. Single-cell expression profiling with the BD Rhapsody Single Cell Analysis System will complement traditional FACS analysis. To confirm the crucial role of T cells, in vitro-expanded individual T cell clones will be transferred. To study the role of antigen presentation on T cell clonality and on disease manifestation, B cells deficient for MHC II and co-stimulation-blocking anti-CD40L antibodies will be used.

- Projects
- 1st Generation
- A: Defining Autoimmune Pre-Disease
- B: Targeting of Autoimmune Pre-Disease
- Associated projects
- Medical doctoral researcher projects
- Concluded projects
- Doctoral researchers
- A1: Exploring the pre-disease phase of autoimmunity in lupus-prone mouse models
- A2: B cell activation in murine lupus
- A3: G protein-coupled receptors orchestrating granulocytes in pemphigoid diseases
- A4: Epitope-dependent autoantibody-mediated skin inflammation in pemphigoid diseases
- A5: Chronic danger signaling as driver of autoimmunity in granulomatosis with polyangiitis
- A6: Combining in-depth immune profiling and multi-omics approaches identifies distinct signatures in the early stage of systemic sclerosis
- A7: CD4+ T cell receptor sequences during progression towards experimental pemphigoid
- A8: The C5aR2 pathway as a novel checkpoint for B cell activation in autoimmunity
- A9: Comprehensive genetic and comorbidity profiling of autoimmune diseases: Integrating UK Biobank, TriNetX and Global Data
- B1: Diet as an intervention in autoimmune pre-disease
- B2: Influence of anti-TNF treatment on B cell responses and the type of IgG Fc glycosylation
- B3: Clinical and experimental investigation of T helper cytokines dysregulation in systemic sclerosis-associated pulmonary arterial hypertension
- Medical doctoral researchers
- Ass. doctoral researchers
- Ass. medical doctoral researchers
- Doctoral researchers
- 2nd Generation
- 1st Generation