Department of Pathology
3-501 Bowen Science Building
51 Newton Road
University of Iowa
Iowa City, IA 52242
Bachelor of Science in Microbiology - University of Kansas
Sepsis is characterized by a systemic infection resulting in organ failure. Sepsis related complications currently account for 33-50% of all hospital deaths. Patients that survive a septic event are more susceptible to infection. The Badovinac lab focuses on CD8 T cells which provide protection against viral and bacterial infections. Our lab has shown that sepsis leads to cell death of both naïve and memory CD8 T cells resulting in increased susceptibility to new, or previously encountered infections.
Tissue-resident memory (TRM) is a recently discovered CD8 T cell subset. These cells survey barrier tissues that are commonly exploited by pathogens to enter the host and cause infection. During a localized infection, TRM rapidly provide protection by recruiting and activating immune cells at the site of pathogen entry. It is not currently known the extent to which sepsis affects TRM. I will start addressing this by elucidating the impact of sepsis on TRM numbers, metabolism and protective capacity.
- Strother RK, DB Danahy, DI Kotov, TA Kucaba, ZR Zacharias, TS Griffith, KL Legge, and VP Badovinac. Polymicrobial sepsis diminishes dendritic cell numbers and function directly contributing to impaired primary CD8 T cell responses in vivo. J Immunol 197: 4301-4311 (2016) [PubMed]
- Danahy DB, RK Strother, VP Badovinac, and TS Griffith. Clinical and experimental sepsis impair T cell-mediated immunity. Crit Rev Immunol 36: 57-74 (2016) [PubMed]
- Newton, A.H., DB Danahy, MA Chan, and SH Benedict, Timely blockade of ICAM-1.LFA-1 interaction prevents disease onset in a mouse model of emphysema. Immunotherapy 7: 621-269 (2015) [PubMed]