Sladjana Skopelja-Gardner, PhD
Title(s)
Assistant Professor of Microbiology and Immunology
Assistant Professor of Medicine
Department(s)
Microbiology and Immunology
Medicine
Education
Geisel School of Medicine at Dartmouth, Ph.D., 2017
Dartmouth College, B.A., 2011
Programs
Molecular and Cellular Biology Graduate Programs
Contact Information
One Medical Center Dr
Borwell 608W
Lebanon NH 03756
Professional Interests
Our research aims to identify how innate immune pathways drive the development of autoimmunity and contribute to disease pathogenesis. We are addressing these questions in models of skin sterile inflammation that are relevant to autoimmune diseases such as systemic lupus erythematosus (SLE) and dermatomyositis (DM), as well as in primary human tissues. With the goal to identify novel therapeutic targets, we are investigating the regulation of type I interferon response as well as neutrophil migration and function.
Cystic fibrosis-related kidney disease-emerging morbidity and disease modifier. Targeting cell-surface VISTA expression on allospecific naive T cells promotes tolerance. Lung-kidney axis in cystic fibrosis: Early urinary markers of kidney injury correlate with neutrophil activation and worse lung function. Lung-Kidney Axis in Cystic Fibrosis: Early Urinary Markers of Kidney Injury Correlate with Neutrophil Activation and Worse Lung Function. Spatial characterization of interface dermatitis in cutaneous lupus reveals novel chemokine ligand-receptor pairs that drive disease. Immune complex-driven neutrophil activation and BAFF release: a link to B cell responses in SLE. Role of the cGAS-STING pathway in systemic and organ-specific diseases. Differential Enhancement of Neutrophil Phagocytosis by Anti-Bactericidal/Permeability-Increasing Protein Antibodies. Killing three birds with one BPI: Bactericidal, opsonic, and anti-inflammatory functions. Bactericidal/Permeability-Increasing Protein Preeminently Mediates Clearance of Pseudomonas aeruginosa In Vivo via CD18-Dependent Phagocytosis. |
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