Research Interest: Immunology
Name | PhD Program | Research Interest | Publications |
---|---|---|
Gjoneska, Elizabeth WEBSITE PUBLICATIONS |
PHD PROGRAM RESEARCH INTEREST |
Neurodegenerative disorders like Alzheimer’s disease (AD) represent a global health emergency. Evidence showing that systemic inflammation can exacerbate cognitive decline during neurodegeneration, including AD, and identification of disease-associated genetic risk variants that perturb function of microglia, the resident brain immune cells, reveal that microglia play an active role in disease progression. Studies in the Gjoneska group aim to elucidate the mechanisms underlying microglia dysfunction during AD. To that end, our group combines cutting edge molecular, cellular and genomic tools together with genetic in vivo approaches to understand how genetic and environmental risk factors alter the function of microglia and contribute to increasing susceptibility to AD. |
Free, Meghan WEBSITE PUBLICATIONS |
PHD PROGRAM RESEARCH INTEREST |
My research focuses on understanding the immunological underpinnings of autoimmune disease, specifically anti-neutrophil cytoplasmic autoantibody (ANCA) vasculitis. We examine CD4+ T cells in the context of disease onset, remission, relapse, and long-term remission off therapy. By studying both autoreactive T cells and regulatory T cells, we aim to create biomarkers of disease activity and potential new targets for immunotherapy. |
Sparkenbaugh, Erica WEBSITE PUBLICATIONS |
PHD PROGRAM RESEARCH INTEREST |
The broad goal in my laboratory is to investigate crosstalk between coagulation and inflammation in animal models of disease. My primary interest is sickle cell disease, a blood disorder caused by a hemoglobin mutation that results in sickling of red blood cells. The primary complications of sickle cell disease are anemia and vaso-occlusive crisis (VOC), as well as chronic inflammation and coagulation activation. VOC is caused by the formation of multicellular aggregates between neutrophils, platelets, sickle red blood cells and the endothelium that is due, in part, to thrombin-dependent activation of protease activated receptor 1 (PAR-1). We are currently investigating how biased agonism of PAR1 with activated protein C (APC) can beneficially influence vaso-occlusive crisis and other pathologies in sickle cell disease. We use a variety of tools, such as transgenic mice, clinically relevant pharmacologic inhibitors, and molecular and cellular biology techniques to study the role of coagulation proteases and protease activated receptors in health and disease. |
Jenson, Justin WEBSITE PUBLICATIONS |
PHD PROGRAM RESEARCH INTEREST |
Our lab studies molecular interactions between bacteria and the viruses that infect them, called phage. For billions of years, phage and bacteria have been locked in a ‘molecular arms race’. To survive, bacteria have evolved many immune systems to protect against infection and, in response, phage have counter-adapted to evade these defenses. Our lab is interested in 1) understanding how these systems work biochemically and structurally and 2) discovering new factors involved in this ‘molecular arms race’. We are particularly interested in systems that share homology with human immune factors. |
Fletcher, Sarah |
PHD PROGRAM RESEARCH INTEREST |
|
Yuan, Runjie |
PHD PROGRAM RESEARCH INTEREST |
|
Wang, Xing |
PHD PROGRAM RESEARCH INTEREST |
|
van Rooyen, Lara |
PHD PROGRAM RESEARCH INTEREST |
|
Trumbo, Aftyn |
PHD PROGRAM RESEARCH INTEREST |
|
Sofian, Christina |
PHD PROGRAM RESEARCH INTEREST |
|