Evidence for the Participation of Soluble Triggering Receptor Expressed on Myeloid Cells-1 in the Systemic Inflammatory Response Syndrome After Multiple Trauma
Abstract:This is the first study providing evidence about the participation of sTREM-1 in posttraumatic SIRS. Its levels are increased and remain constant over time in patients who did not develop any complications whereas it seems to behave as an anti-inflammatory mediator.
“…We report that after DE exposure, mice that consumed M. tea had 2 fold or higher increases in the levels of proinflammatory/chemotactic cytokines (IL-1β and α, KC, M-CSF, RANTES, MIP-2 and MIP1-α, in the lung, as compared to mice that drank water. We also observed increases in immunosuppressive cytokines IL-6, IL-1Ra and TREM-1 (De Bie et al, 2002;Okada et al, 1995;Little and Cruikshank, 2004;Gibot and Massin, 2006;Giamarellos-Bourboulis et al, 2008).…”
Section: Discussionmentioning
confidence: 64%
“…The membrane form of TREM-1 can be cleaved into a soluble form, sTREM that is released into microenvironment (Gomez-Pina et al, 2007). While, high levels of sTREM-1 have been found in patients with severe forms of allergic asthma (Bucova et al, 2012), it has been suggested that sTREM-1 may have an antiinflammatory role, by acting through a mechanism whereby sTREM blocks interactions of membrane-bound TREM-1 with its natural ligand in a way similar to the recognized interaction between the soluble form of the TNF-α receptor and membrane TNF-α receptor (Gibot and Massin, 2006; Science Publications -Bourboulis et al, 2008). Furthermore, it has been suggested that sTREM could be used as therapeutic for inflammatory conditions such as rheumatoid arthritis and sepsis (Kim et al, 2012;Wang et al, 2012).…”
Plant based products represent a promising alternative to conventional treatments for inflammation. Moringa oleifera Lam is a tree rich in proteins, vitamins, minerals and a variety of phytochemcals with health benefits. Among the reported health benefits are antioxidant and anti-inflammatory properties. The purpose of this study was to investigate whether tea brewed from dried Moringa leaves would abrogate inflammation in a mouse model of acute lung inflammation induced by LPS or extracts prepared from dust collected from a swine confinement facility (DE). Mice were offered water or Moringa tea for seven days. Tea consumption was significantly greater than that of water consumption on days 1 and 6, but there were no significant differences in weight gain or food consumption. On day seven, mice from both groups were forced to inhale, via intranasal challenge, either Phosphate Buffered Saline (PBS), Lipopolysaccharide (LPS) [10 µg mLCompared to mice that drank water, mice that drank Moringa tea had significantly less protein (p<0.05) and cellular influx (p<0.0001) into the lung after inhalation of 10% DE. No difference in neutrophil migration into the lungs of water and M. tea groups after LPS or DE challenge was detected. But mice that drank tea had significantly (p<0.05) more neutrophils with apoptotic morphology after DE challenge. TNF-α expression 24 h after inhalation of 10% DE, was significantly higher (p<0.05) in lungs of M. tea mouse group as compared to water group. This increase in TNF-α was accompanied by higher levels of pro and anti-inflammatory cytokines. Finally, activation of c-Jun N-terminal Kinase (JNK) in lungs of M. tea+DE group 24 h post inhalation was decreased. Taken together these results suggest that Moringa oleifera leaf tea exerts antiinflammatory properties on acute lung inflammation induced by swine confinement dust through a mechanism involving neutrophil regulation and JNK activation.
“…We report that after DE exposure, mice that consumed M. tea had 2 fold or higher increases in the levels of proinflammatory/chemotactic cytokines (IL-1β and α, KC, M-CSF, RANTES, MIP-2 and MIP1-α, in the lung, as compared to mice that drank water. We also observed increases in immunosuppressive cytokines IL-6, IL-1Ra and TREM-1 (De Bie et al, 2002;Okada et al, 1995;Little and Cruikshank, 2004;Gibot and Massin, 2006;Giamarellos-Bourboulis et al, 2008).…”
Section: Discussionmentioning
confidence: 64%
“…The membrane form of TREM-1 can be cleaved into a soluble form, sTREM that is released into microenvironment (Gomez-Pina et al, 2007). While, high levels of sTREM-1 have been found in patients with severe forms of allergic asthma (Bucova et al, 2012), it has been suggested that sTREM-1 may have an antiinflammatory role, by acting through a mechanism whereby sTREM blocks interactions of membrane-bound TREM-1 with its natural ligand in a way similar to the recognized interaction between the soluble form of the TNF-α receptor and membrane TNF-α receptor (Gibot and Massin, 2006; Science Publications -Bourboulis et al, 2008). Furthermore, it has been suggested that sTREM could be used as therapeutic for inflammatory conditions such as rheumatoid arthritis and sepsis (Kim et al, 2012;Wang et al, 2012).…”
Plant based products represent a promising alternative to conventional treatments for inflammation. Moringa oleifera Lam is a tree rich in proteins, vitamins, minerals and a variety of phytochemcals with health benefits. Among the reported health benefits are antioxidant and anti-inflammatory properties. The purpose of this study was to investigate whether tea brewed from dried Moringa leaves would abrogate inflammation in a mouse model of acute lung inflammation induced by LPS or extracts prepared from dust collected from a swine confinement facility (DE). Mice were offered water or Moringa tea for seven days. Tea consumption was significantly greater than that of water consumption on days 1 and 6, but there were no significant differences in weight gain or food consumption. On day seven, mice from both groups were forced to inhale, via intranasal challenge, either Phosphate Buffered Saline (PBS), Lipopolysaccharide (LPS) [10 µg mLCompared to mice that drank water, mice that drank Moringa tea had significantly less protein (p<0.05) and cellular influx (p<0.0001) into the lung after inhalation of 10% DE. No difference in neutrophil migration into the lungs of water and M. tea groups after LPS or DE challenge was detected. But mice that drank tea had significantly (p<0.05) more neutrophils with apoptotic morphology after DE challenge. TNF-α expression 24 h after inhalation of 10% DE, was significantly higher (p<0.05) in lungs of M. tea mouse group as compared to water group. This increase in TNF-α was accompanied by higher levels of pro and anti-inflammatory cytokines. Finally, activation of c-Jun N-terminal Kinase (JNK) in lungs of M. tea+DE group 24 h post inhalation was decreased. Taken together these results suggest that Moringa oleifera leaf tea exerts antiinflammatory properties on acute lung inflammation induced by swine confinement dust through a mechanism involving neutrophil regulation and JNK activation.
“…IL-6: (1) ARDS; two studies [37,45] could not relate ARDS to IL-6 concentration alterations, whereas two other studies [48,51] found a positive correlation (Table 2); (2) Sepsis; five studies [35,41,46,47,53] found an increased IL-6 production to be predictive for the development of sepsis, whereas five other studies [28,29,38,39,55] did not (Table 3); (3) MODS; all five prospective cohort studies [3,28,34,46,51] concluded that IL-6 is markedly increased in the early development of MODS ( Dekker ABE et al . Do cytokines predict polytrauma outcome IL-10: (1) Three studies, two prospective [54,57] and one retrospective [14] , could not relate the serum IL-10 concentrations to the development of ARDS.…”
Section: Value Of Main Cytokine Concentrations For Predicting Complicmentioning
confidence: 89%
“…(1) Three studies found no relation between TNF-a and development of ARDS [37,45,51] ; (2) One study [55] concluded that concentrations were not related to development of sepsis, while one study [50] found significantly increased concentrations in septic patients; (3) Of the four studies reporting on TNF-a concentrations after trauma, two studies [31,51] found TNF-a to be related to the development of MODS, and two studies [3,57] could not relate serum concentrations [35] 2009 P-coh 1032 IL-6 10% 2…”
Section: Tnf-amentioning
confidence: 99%
“…(1) Two prospective cohort studies [37,48] reported a positive correlation between increased serum IL-8 concentrations and development of ARDS, whereas one [45] found no predictive value; (2) Two studies [38,55] reported that IL-8 was not significantly different between patients developing sepsis and those with an uneventful posttraumatic course; (3) One cohort study [3] found a higher IL-8 serum concentration in patients with MODS, which could however not predict the development of multiorgan dysfunction; and (4) Of the six included studies, four prospective studies [27,32,36,56] concluded that IL-8 is significantly higher in MOF. Two prospective studies [11,42] also found a significantly increased serum concentration, but concluded that this could not be translated into a predictive value for adverse outcome.…”
AIM:To investigate posttraumatic cytokine alterations and their value for predicting complications and mortality in polytraumatized patients.
METHODS:Studies on the use of specific cytokines to predict the development of complications and mortality were identified in MEDLINE, EMBASE, Web of Science and the Cochrane Library. Of included studies, relevant data were extracted and study quality was scored.
RESULTS:Forty-two studies published between 1988 and 2015 were identified, including 28 cohort studies and 14 "nested" case-control studies. Most studies investigated the cytokines interleukin (IL)-6, IL-8, IL-10 and tumor necrosis factor (TNF-a). IL-6 seems related to muliorgan dysfunction syndrome, multiorgan failure (MOF) and mortality; IL-8 appears altered in acute respiratory distress syndrome, MOF and mortality; IL-10 alterations seem to precede sepsis and MOF; and TNF-a seems related to MOF.
CONCLUSION:Cytokine secretion patterns appear to be different for patients developing complications when compared to patients with uneventful posttraumatic course. More research is needed to strengthen the evidence for clinical relevance of these cytokines.
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