Dr. Brantly’s laboratory specializes in alpha-1 antitrypsin deficiency, which manifests mainly as lung and liver injury. Studies are centralized around characterization of alveolar macrophage function, hepatic fibrosis, gastrointestinal microbiota, and extracellular vesicles. We are interested in understanding how misfolded alpha-1 protein affects cellular signaling and degradation machinery.
Dr. Bryant’s lab is interested in understanding the impact that immune cells play in patients with pulmonary hypertension. We primarily use pre-clinical models of high blood pressure in the lungs to determine how inflammation contributes to changes in pulmonary vasculature. Our hope is that this work will yield novel targets for drug therapies, especially in those patients with pulmonary hypertension secondary to chronic lung disease such as interstitial lung disease.
Dr. Jin’s lab has a keen interest in understanding the in vivo mechanism of lung mucosal tolerance and developing new therapeutics for chronic lung diseases, e.g asthma and COPD that are the 3rd leading cause of death in the U.S. Dr. Jin’s lab is also interested in understanding how common human STING genetic variants influence human health and medicine.
Dr. Mehrad’s lab specializes in Interstitial lung diseases; a heterogeneous group of lung diseases defined by chronic inflammation and fibrosis. The lab has 3 main areas of focus 1) Fibrocytes 2) Host defense mechanisms in invasive aspergillosis (3) Experimental therapy for Gram-negative bacterial infections.
Dr. Moser’s lab studies how antibody responses are triggered. Antibodies comprise a powerful arm of the immune system. Antibodies protect from infection, but can also cause autoimmune disease and transplant rejection. Before becoming antibody-secreting cells, activated B cells receive and respond to a multitude of cues that instruct the antibody response. Dr. Moser’s lab studies how protein modifications within the B cells shift the antibody program to induce protective or pathologic antibodies. This research will help design therapies to better elicit protective antibodies and inhibit disease-causing antibodies.
Dr. Mulligan’s laboratory focuses on understanding the mechanisms that initiate and exacerbate inflammatory diseases of the upper and lower airways with a significant emphasis on chronic rhinosinusitis (CRS). CRS affects up to 16% of the US population with direct costs of nearly $22 billion per year. Its negative impact on quality of life exceeds other chronic conditions, such as heart failure and chronic obstructive pulmonary disease. Furthermore, CRS is highly prevalent in severe asthmatics and is associated with a greater frequency of exacerbations. Our laboratory works closely with clinicians and scientists spanning multiple disciplines allowing us to conduct cutting edge translational research using human tissue and rodent models.
Dr. Schaller’s lab studies the interactions between immune cells and pathogens that occur in the lung, with a particular interest in Mycobacterium Tuberculosis infection. Over 1/3 of the world’s population is infected with M. tb and there is no vaccine available that can sterilize the infection. Understanding the immune response to this pathogen is key to the development of new vaccines and treatments for this chronic condition.