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dc.creatorMerz, Tobias M.-
dc.creatorPereira, Adriano J.-
dc.creatorSchürch, Roger-
dc.creatorSchefold, Joerg C.-
dc.creatorJakob, Stephan M.-
dc.creatorTakala, Jukka-
dc.creatorDjafarzadeh, Siamak-
dc.date.accessioned2018-06-28T12:29:35Z-
dc.date.available2018-06-28T12:29:35Z-
dc.date.issued2017-06-
dc.identifier.citationMERZ, T. M. et al. Mitochondrial function of immune cells in septic shock: a prospective observational cohort study. PLoS ONE, [S.l.], v. 12, n. 6, June 2017.pt_BR
dc.identifier.urihttp://journals.plos.org/plosone/article?id=10.1371/journal.pone.0178946pt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/29513-
dc.description.abstractBackground: reduced cellular ATP synthesis due to impaired mitochondrial function of immune cells may be a factor influencing the immune response in septic shock. We investigate changes in mitochondrial function and bioenergetics of human monocytes and lymphocyte subsets. Methods: thirty patients with septic shock were studied at ICU admission, after 24 and 48 hours, and after resolution of shock. Enzymatic activities of citrate synthase and mitochondrial complexes I, IV, and ATP synthase and ATP content of monocytes, T-cells and B-cells and pro-inflammatory (IL-1β and IL-6) and anti-inflammatory (IL-10) cytokine plasma concentrations were compared to samples from 20 healthy volunteers. Results: large variations in mitochondrial enzymatic activities of immune cells of septic patients were detected. In monocytes, maximum levels of citrate synthase activity in sepsis were significantly lower when compared to controls (p = 0.021). Maximum relative enzymatic activity (ratio relative to citrate synthase activity) of complex I (p<0.001), complex IV (p = 0.017) and ATP synthase (p<0.001) were significantly higher. In T-cells, maximum levels of citrate synthase (p = 0.583) and relative complex IV (p = 0.602) activity did not differ between patients and controls, whereas levels of relative complex I (p = 0.006) and ATP synthase (p = 0.032) were significantly higher in septic patients. In B-cells of patients, maximum levels of citrate synthase activity (p = 0.004) and relative complex I (p<0.001) were significantly higher, and mean levels of relative complex IV (p = 0.042) lower than the control values, whereas relative ATP synthase activity did not differ (p = 1.0). No significant difference in cellular ATP content was detected in any cell line (p = 0.142–0.519). No significant correlations between specific cytokines and parameters of mitochondrial enzymatic activities or ATP content were observed. Conclusions: significant changes of mitochondrial enzymatic activities occur in human peripheral blood immune cells in septic shock when compared to healthy controls. Assessed sub-types of immune cells showed differing patterns of regulation. Total ATP-content of human immune cells did not differ between patients in septic shock and healthy volunteers.pt_BR
dc.languageen_USpt_BR
dc.publisherPLOSpt_BR
dc.rightsrestrictAccesspt_BR
dc.sourcePLoS ONEpt_BR
dc.subjectOxidative phosphorylation (OXPHOS)pt_BR
dc.subjectAdenosine triphosphate (ATP)pt_BR
dc.subjectMitochondriapt_BR
dc.subjectImmune cellspt_BR
dc.titleMitochondrial function of immune cells in septic shock: a prospective observational cohort studypt_BR
dc.typeArtigopt_BR
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