Administration of endotoxin to humans allows a unique way to evaluate the early inflammatory reactions that occur during infection. Characterizing these responses and the mechanisms that control them is important because these inflammatory responses contribute to the development of septic shock and organ failure. Protocol 92-CC-0141 is evaluating acute inflammatory responses to endotoxin.The development of tolerance to inflammatory stimuli during critical illness has important implications for the application of anti-inflammatory therapies and the prevention of organ failure during sepsis. To evaluate mechanisms of cell priming and endotoxin tolerance in vivo, subjects will be given two doses of intravenous endotoxin at 3- to 6-hour intervals. Systemic hemodynamics and inflammatory responses will be assessed. Using this method of endotoxin administration, we hope to gather information regarding control of inflammatory responses induced by endotoxin, and to gain insight into mechanisms of tolerance. In addition to measuring circulating inflammatory mediators (e.g., tumor necrosis factor, Interleukin-1), we will evaluate peripheral blood cells to assess the changes in cell surface receptors for acute phase cytokines as well as endotoxin.Currently inactive.

Agency
National Institute of Health (NIH)
Institute
Clinical Center (CLC)
Type
Intramural Research (Z01)
Project #
1Z01CL000174-03
Application #
6103582
Study Section
Special Emphasis Panel (CCMD)
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Clinical Center
Department
Type
DUNS #
City
State
Country
United States
Zip Code