Assistant Adjunct Professor of Pediatrics
Contact InfoBox 0665
35 Medical Center Way, Rm 900
San Francisco, CA. 94143
Phone: (415) 502-2525
- 1993–1997, Dalhousie University, Halifax, Nova Scotia, Canada. B.Sc. (Hons)
- 1997–2002, Harvard Medical School, Harvard-MIT Division of Health Sciences and Technology, M.D.
- 2002–2003, Children’s Hospital, Boston, Department of Medicine, Internship in Pediatrics
- 2003–2005, Children’s Hospital, Boston, Department of Medicine, Residency in Pediatrics
- 2005–2009, University of California San Francisco, Division of Neonatology, Fellowship in Neonatal-Perinatal Medicine
- 2010, Neonatal-Perinatal Medicine
- 2005, American Board of Pediatrics, General Pediatrics
- Development of the fetal and neonatal immune system.
- Immune system regulation in HIV and other chronic infectious diseases.
UCSF Program Affiliations
Dr. Trevor Burt earned his medical degree at Harvard Medical School and the Massachusetts Institute of Technology in the Harvard-MIT Division of Health Sciences and Technology (HST), where he worked in the laboratory of Drs. Michael Grusby and Laurie Glimcher studying the molecular basis of T cell differentiation. Subsequently, he completed an internship and residency in Pediatrics at Children's Hospital Boston and Boston Medical Center in the Boston Combined Residency Program (BCRP). He completed a post-doctoral fellowship in the laboratory of Dr. Mike McCune in the UCSF Division of Experimental Medicine, and a clinical fellowship in Neonatal-Perinatal Medicine in the UCSF Division of Neonatology. He is a former fellow of the Pediatric Scientist Development Program.
A coordinated response of both the innate and acquired arms of the immune system is essential to effectively fight infectious diseases. An insufficient immune response may lead to overwhelming infection. In the case of many pathogens, however, and overly aggressive immune response can exacerbate and prolong the course of infection. Dr. Burt’s research interests have focused on how the human immune system responds to, and regulates, its response to the Human Immunodeficiency Virus (HIV) and other chronic infections. Specifically, he is interested in the role of the immuno-modulatory enzymes Heme Oxygenase-1 (HO-1) and Indoleamine 2,3, Dioxygenase (IDO) in altering the immune response to HIV. He is also focused on the development of the human fetal and newborn immune system, and how the developmental state of the immune system can influence its response to infection.