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We began analyzing https://ccforum.biomedcentral.com/articles/10.1186/cc9233, but it redirected us to https://ccforum.biomedcentral.com/articles/10.1186/cc9233. The analysis below is for the second page.

Title[redir]:
Plasma concentrations of Gas6 (growth arrest specific protein 6) and its soluble tyrosine kinase receptor sAxl in sepsis and systemic inflammatory response syndromes | Critical Care | Full Text
Description:
Introduction Gas6, the protein product of the growth arrest specific gene 6, is present in human circulation at subnanomolar concentrations. It is secreted by endothelial cells and is important for the activation of endothelium during inflammation. Axl, the tyrosine kinase receptor for Gas6, is also present in endothelium and can be cleaved and released into the circulation. The soluble of form Axl (sAxl), which is present in plasma, can bind Gas6 and inhibit Axl-mediated cell signalling. Methods We have developed reproducible and accurate enzyme-linked immunosorbent assays for both Gas6 and sAxl and used them to investigate plasma samples from 70 patients with severe sepsis, 99 patients with sepsis, 42 patients with various infections causing fever but no systemic inflammatory response syndrome (SIRS), 20 patients with SIRS without verified infection, and 100 blood donors that served as controls. Correlations between Gas6 and sAxl concentrations and other commonly used analytes were investigated. Results The patients with severe sepsis, sepsis, infection or SIRS had all increased concentrations of Gas6, approximately double compared to what was found in the controls. The concentrations of sAxl were also increased in the patient groups compared to the controls. Gas6 correlated with C-reactive protein, procalcitonin and interleukin 6, whereas sAxl correlated to bilirubin and procalcitonin. Conclusions We can confirm results of earlier studies showing that circulating Gas6 is increased in sepsis and related syndromes. sAxl is increased, but less pronounced than Gas6. The concentrations of Gas6 and sAxl correlate with a number of inflammatory markers, suggesting a role in systemic inflammation.

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Keywords {🔍}

gas, saxl, sepsis, patients, article, concentrations, pubmed, plasma, sirs, increased, google, scholar, protein, cas, axl, severe, groups, failure, inflammatory, care, infection, blood, patient, study, organ, growth, response, number, cells, tyrosine, cell, table, authors, data, soluble, kinase, receptor, dahlbäck, controls, compared, procalcitonin, analysis, systemic, samples, infections, found, correlated, related, university, criteria,

Topics {✒️}

vitamin k-dependent ligands vitamin k-dependent protein pi3 kinase/akt pathway growth arrest-specific gene tyrosine kinase receptor critical care medicine full size image receptor tyrosine kinases authors scientific editing privacy choices/manage cookies tyrosine kinase receptors complex clinical syndrome article ekman bmc damaging host response innate immune response international consensus conference related inflammatory syndromes severe sepsis group swedish research council adam10-dependent cleavage severe inflammatory reactions inflammatory reactions suggests increased signaling occurs combined severe sepsis significance levels observed severe inflammatory states related inflammatory conditions authors’ original file acute phase protein systolic blood pressure blood coagulation cascade inflammatory response european economic area catching polyclonal antibody biotinylated secondary antibody standard curve prepared rank correlation coefficient garcia de frutos di santo jp hansa medical ab c-reactive protein experiencing kidney failure 50 mm tris-hcl biomed central gas6 induced signaling genes specifically expressed urinary tract infections upper respiratory infections author information authors

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      headline:Plasma concentrations of Gas6 (growth arrest specific protein 6) and its soluble tyrosine kinase receptor sAxl in sepsis and systemic inflammatory response syndromes
      description:Gas6, the protein product of the growth arrest specific gene 6, is present in human circulation at subnanomolar concentrations. It is secreted by endothelial cells and is important for the activation of endothelium during inflammation. Axl, the tyrosine kinase receptor for Gas6, is also present in endothelium and can be cleaved and released into the circulation. The soluble of form Axl (sAxl), which is present in plasma, can bind Gas6 and inhibit Axl-mediated cell signalling. We have developed reproducible and accurate enzyme-linked immunosorbent assays for both Gas6 and sAxl and used them to investigate plasma samples from 70 patients with severe sepsis, 99 patients with sepsis, 42 patients with various infections causing fever but no systemic inflammatory response syndrome (SIRS), 20 patients with SIRS without verified infection, and 100 blood donors that served as controls. Correlations between Gas6 and sAxl concentrations and other commonly used analytes were investigated. The patients with severe sepsis, sepsis, infection or SIRS had all increased concentrations of Gas6, approximately double compared to what was found in the controls. The concentrations of sAxl were also increased in the patient groups compared to the controls. Gas6 correlated with C-reactive protein, procalcitonin and interleukin 6, whereas sAxl correlated to bilirubin and procalcitonin. We can confirm results of earlier studies showing that circulating Gas6 is increased in sepsis and related syndromes. sAxl is increased, but less pronounced than Gas6. The concentrations of Gas6 and sAxl correlate with a number of inflammatory markers, suggesting a role in systemic inflammation.
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