Area of research
Immunology · Molecular Biology
Research interest
Research interests include T-cell and B-cell Immunology, Immune Cell Function and Interaction, Single-cell and spatial transcriptomics, and SARS-CoV-2 and COVID-19 Research.
Polyamines regulate adaptive antitumor immunity by functional specialization of regulatory T cells
Single-cell insights into immune dysregulation in rheumatoid arthritis flare versus drug-free remission.
Recruitment of plasma cells from IL-21-dependent and IL-21-independent immune reactions to the bone marrow
Immune signatures of checkpoint inhibitor-induced autoimmunity-A focus on neurotoxicity.
Recruitment of plasma cells from IL-21-dependent and IL-21-independent immune reactions to the bone marrow.
Prophylactic antibodies inhibit spike-specific T and B cell responses after COVID-19 vaccination.
Spatially Resolved Multi-Omics Single-Cell Analyses Inform Mechanisms of Immune Dysfunction in Pancreatic Cancer
Daratumumab for the treatment of refractory ANCA-associated vasculitis
Immune signatures of checkpoint inhibitor-induced autoimmunity—A focus on neurotoxicity
SARS-CoV-2 specific plasma cells acquire long-lived phenotypes in human bone marrow.
Immune cell profiling reveals natural killer and T cell subpopulations to be associated with atopic dermatitis severity.
Recruitment of plasma cells to the bone marrow in primary and secondary immune reactions
Immune cell profiling reveals natural killer and T cell subpopulations to be associated with atopic dermatitis severity
Differential durability of humoral and T cell immunity after two and three BNT162b2 vaccinations in adults aged >80 years
Pro-inflammatory innate-like T cells are expanded in the blood and inflamed intestine in Crohn’s Disease
NASH limits anti-tumour surveillance in immunotherapy-treated HCC
NASH limits anti-tumour surveillance in immunotherapy-treated HCC.
Deep spatial profiling of human COVID-19 brains reveals neuroinflammation with distinct microanatomical microglia-T-cell interactions
Characterization of pre-existing and induced SARS-CoV-2-specific CD8<sup>+</sup> T cells.
Complement activation induces excessive T cell cytotoxicity in severe COVID-19
Dysregulated CD38 Expression on Peripheral Blood Immune Cell Subsets in SLE
Dysregulated CD38 Expression on Peripheral Blood Immune Cell Subsets in SLE.
Deep phenotypical characterization of human CD3<sup>+</sup> CD56<sup>+</sup> T cells by mass cytometry.
The Worm-Specific Immune Response in Multiple Sclerosis Patients Receiving Controlled <i>Trichuris suis</i> Ova Immunotherapy.
Severe COVID-19 Is Marked by a Dysregulated Myeloid Cell Compartment
Targeting CD38 with Daratumumab in Refractory Systemic Lupus Erythematosus
<i> IGLV3-21 <i>*</i> 01 </i> is an inherited risk factor for CLL through the acquisition of a single-point mutation enabling autonomous BCR signaling
<i>IGLV3-21<i>*</i>01</i> is an inherited risk factor for CLL through the acquisition of a single-point mutation enabling autonomous BCR signaling.
Deep phenotypical characterization of human CD3 <sup>+</sup> CD56 <sup>+</sup> T cells by mass cytometry
Deep Phenotyping of Urinary Leukocytes by Mass Cytometry Reveals a Leukocyte Signature for Early and Non-Invasive Prediction of Response to Treatment in Active Lupus Nephritis.