Mitochondrial Function of Immune Cells in Sepsis (MitoSepsis)
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|ClinicalTrials.gov Identifier: NCT01600989|
Recruitment Status : Completed
First Posted : May 17, 2012
Last Update Posted : April 25, 2014
Introduction: Evidence suggests that sepsis and septic shock severely impair mitochondria and that the resulting mitochondrial dysfunction is related to the severity and outcome of the resulting organ dysfunction. In sepsis mitochondrial abnormalities - biochemical and ultrastructural - have been recognized in multiple organs, including liver, kidney, skeletal and heart muscle tissue and blood cells. Circulating immune cells play an important role in the pathophysiology of sepsis. Stimulation of the immune system alters the energy requirements of immune cells; down-regulation of immune-cell activity has been associated with prolonged sepsis and unfavourable outcome. The aim of the project is to comprehensively investigate changes in mitochondrial function of immune cells in patients with severe sepsis and septic shock. The following main hypotheses will be evaluated:
- Severe sepsis and septic shock leads to increased energy requirements of immune cells and to an increase in mitochondrial enzyme activities and energy production.
- Changes of mitochondrial function in human immune cells are associated with alterations in clinical and laboratory markers of severity of sepsis.
- Prolonged sepsis and unfavourable outcome is associated with down regulation of mitochondrial function.
Methods: A total of 30 adult patients admitted to the intensive care unit (ICU) due to severe sepsis or septic shock will be included in the study; 30 healthy volunteers serve as controls. Patients with any type of chronic infectious, inflammatory or autoimmune diseases, after transplantations or receiving immunosuppressive agents are excluded.
Collected baseline characteristics include patient demographics, diagnosis and severity of illness scores at the time of admission. Daily collected follow up data include clinical and laboratory parameters of organ dysfunction, use of vasopressors/inotropes, use of antibiotics, use of steroids and results of microbiological cultures/stains.
Negative identification and isolation of monocytes, B cells and CD4 T cells will be performed daily from ICU admission to discharge using an antibody-antigen mediated immunomagnetic cell isolation procedure that depletes all blood cells except the specific target cells. Mitochondrial function of immune cells will be assessed by measurement of mitochondrial complex activity for complexes I to IV by a standard titration protocol. Additionally, the levels of pro- and anti-inflammatory cytokines (Interleukin (IL)-1, IL-6, IL-10, TNF-α) will be assessed throughout the stay in the ICU. For comparison mitochondrial function of of monocytes, B cells and CD4 T cells and cytokine levels will be measured in a group of 10 healthy volunteers.
Analysis plan: Changes in mitochondrial function of immune cells over time compared to a healthy control group and during the course of severe sepsis and septic shock is the main outcome parameter of this study. Assessed predictors are determined by the severity of the underlying septic condition and include clinical and laboratory evidence for dysfunction of vital organ systems and changes in levels of inflammatory and anti-inflammatory cytokines.
|Condition or disease||Intervention/treatment|
|Shock, Septic||Other: blood sampling|
|Study Type :||Observational|
|Actual Enrollment :||60 participants|
|Official Title:||Mitochondrial Function of Immune Cells in Severe Sepsis and Septic Shock - a Prospective Observational Cohort Study|
|Study Start Date :||May 2012|
|Actual Primary Completion Date :||October 2013|
|Actual Study Completion Date :||November 2013|
Patients with severe sepsis / septic shock
30 Adult patients (age > 18years), with severe sepsis or septic shock as defined by the 2001 SCCM/ESICM/ACCP/ATS/SIS International Sepsis Definitions Conference guidelines at the time of admission to ICU.
Other: blood sampling
Blood samples will be taken at ICU admission, and 24h and 48h after admission, and at time of resolution of sepsis
Other: blood sampling
Blood samples will be taken twice at a 7 day interval
- Mitochondrial function of immune cells [ Time Frame: At the time of ICU admission ]
- Change from baseline in mitochondrial function of immune cells [ Time Frame: 24 hours after ICU admission ]
- Change from baseline in mitochondrial function of immune cells [ Time Frame: 48 hours after ICU admission ]
- Change from baseline in mitochondrial function of immune cells [ Time Frame: At time of resoltion of sepsis, expected to be after 5 days ]
- Levels of cytokines (of IL-1, IL-6, IL-10 and TNFa) [ Time Frame: At ICU admission, 24h and 48h after admission, & at time of resolution of sepsis (expected to be after 5 days) ]
- ICU mortality [ Time Frame: At time of dismissal from ICU, expected to be after 7 days ]
Biospecimen Retention: Samples With DNA
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01600989
|Department of Intensive Care Medicine, Bern University Hospital (Inselspital) and University of Bern|
|Bern, Switzerland, 3010|
|Study Chair:||Tobias Merz||Department of Intensive Care Medicine, Bern University Hospital (Inselspital) and University of Bern|