Dorian McGavern, Ph.D.
Viral Immunology and Intravital Imaging Section
Building 10, Room 5N240C
10 Center Drive
Bethesda, MD 20892-1430
My laboratory focuses on innate and adaptive immune responses to acute and persistent infection of the central nervous system (CNS) as well as sterile immune responses that develop following mild traumatic brain injury. The CNS is an immunologically specialized tissue containing a population of nonreplicative cells (neurons) responsible for a symphony of electrochemical signaling. The communication between neurons is exceedingly complex and contributes to nearly every aspect of our day-to-day functions. The immune system is equally complex (possessing both innate and adaptive components) and is assigned to the tasks of warding off microbes that invade all parts of the body as well as dealing with damaged tissues. For this reason, the immune system is highly mobile and equipped with effector mechanisms that neutralize pathogens and also molecules that facilitate tissue repair. Despite this balance, immune cells sometimes employ mechanisms that further damage tissues following infection or injury. From an immunological perspective, the CNS is an interesting compartment because it must preserve neuronal function while still enabling immune cells to survey the environment for pathogens and injury. The CNS and immune systems communicate with one another during states of health and disease, and it is the unique dialogue between two systems that guides much of our research. We focus specifically on immune cell surveillance of the infected CNS, pathogenesis of viral meningitis (a disease of the CNS lining), viral encephalitis, mechanisms that give rise to viral persistence, therapeutic approaches to purge infections, the pathogenesis of cerebral malaria (a disease caused by the parasite Plasmodium berghei), and immune reactions to traumatic brain injury. We use many contemporary approaches to gain novel insights into these research areas, the most exciting of which is intravital two-photon microscopy. This approach allows us to watch immune cells clear pathogens, cause diseases, or repair damaged tissues in real-time. Overall, our laboratory crosses the disciplines of virology/microbiology, immunology, and neuroscience in order to provide a comprehensive understanding of the different scenarios that unfold when the CNS is invaded by pathogens or is damaged by injury.
Swanson PA 2nd, Hart GT, Russo MV, Nayak D, Yazew T, Peña M, Khan SM, Janse CJ, Pierce SK, McGavern DB. CD8+ T Cells Induce Fatal Brainstem Pathology during Cerebral Malaria via Luminal Antigen-Specific Engagement of Brain Vasculature. PLoS Pathog. 2016;12(12):e1006022.
Moseman EA, Wu T, de la Torre JC, Schwartzberg PL, McGavern DB. Type I interferon suppresses virus-specific B cell responses by modulating CD8<sup>+</sup> T cell differentiation. Sci Immunol. 2016;1(4).
Herz J, Johnson KR, McGavern DB. Therapeutic antiviral T cells noncytopathically clear persistently infected microglia after conversion into antigen-presenting cells. J Exp Med. 2015;212(8):1153-69.
Nayak D, Roth TL, McGavern DB. Microglia development and function. Annu Rev Immunol. 2014;32:367-402.
Roth TL, Nayak D, Atanasijevic T, Koretsky AP, Latour LL, McGavern DB. Transcranial amelioration of inflammation and cell death after brain injury. Nature. 2014;505(7482):223-8.
Related Scientific Focus Areas
Microbiology and Infectious Diseases
This page was last updated on May 14th, 2018