Area of research
Pathology and Forensic Medicine · Immunology
Research interest
Research interests include Systemic Sclerosis and Related Diseases, Immunotherapy and Immune Responses, Immune cells in cancer, and Inflammatory Myopathies and Dermatomyositis.
Nanobody-liposomes as novel cancer vaccine platform to efficiently stimulate T cell immunity
Impaired LAIR-1-mediated immune control due to collagen degradation in fibrosis
CXCL4 drives fibrosis by promoting several key cellular and molecular processes
CD169 Defines Activated CD14+ Monocytes With Enhanced CD8+ T Cell Activation Capacity
Implication of miR-126 and miR-139-5p in Plasmacytoid Dendritic Cell Dysregulation in Systemic Sclerosis
Liposome induction of CD8+ T cell responses depends on CD169+ macrophages and Batf3-dependent dendritic cells and is enhanced by GM3 inclusion
Hypoxia and TLR9 activation drive CXCL4 production in systemic sclerosis plasmacytoid dendritic cells via mtROS and HIF-2α
Selective tumor antigen vaccine delivery to human CD169 <sup>+</sup> antigen-presenting cells using ganglioside-liposomes
Longitudinal analysis of T-cell receptor repertoires reveals persistence of antigen-driven CD4+ and CD8+ T-cell clusters in systemic sclerosis
Optimization of Liposomes for Antigen Targeting to Splenic CD169+ Macrophages
Histone modifications underlie monocyte dysregulation in patients with systemic sclerosis, underlining the treatment potential of epigenetic targeting
Cytometry by time of flight identifies distinct signatures in patients with systemic sclerosis, systemic lupus erythematosus and Sjögrens syndrome
Low RUNX3 expression alters dendritic cell function in patients with systemic sclerosis and contributes to enhanced fibrosis
Induction of Inflammation and Fibrosis by Semaphorin 4A in Systemic Sclerosis
Serum microRNA screening and functional studies reveal miR-483-5p as a potential driver of fibrosis in systemic sclerosis
CXCL4 is a novel inducer of human Th17 cells and correlates with IL‐17 and IL‐22 in psoriatic arthritis
CXCL4 Exposure Potentiates TLR-Driven Polarization of Human Monocyte-Derived Dendritic Cells and Increases Stimulation of T Cells
Dendritic cells in systemic sclerosis: Advances from human and mice studies
Chronic Toll-like receptor 4 stimulation in skin induces inflammation, macrophage activation, transforming growth factor beta signature gene expression, and fibrosis
Proteome-wide Analysis and CXCL4 as a Biomarker in Systemic Sclerosis
Global chemokine expression in systemic sclerosis (SSc): CCL19 expression correlates with vascular inflammation in SSc skin
Thymic Stromal Lymphopoietin Is Up‐Regulated in the Skin of Patients With Systemic Sclerosis and Induces Profibrotic Genes and Intracellular Signaling That Overlap With Those Induced by Interleukin‐13 and Transforming Growth Factor β