nakamura 2008 critical care

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Crit Care. 2008; 12(Suppl 2): P194. Published online 2008 Mar 13. doi: 10.118!""41# PMC$%: PMC4088## Early elevation of plasma soluble CD14 subtype, a novel biomarker for sepsis, in a rabbit cecal ligation and puncture model M &a'a ura 1 * *a'eu"hi 1 + &aito 1 + Shira'a,a 1 - osa'a 1 / -a asa'i 1 and S /urusa'o 1 uthor in or ation rti"le notes Cop ri ht and 5i"ense in or ation 6o to: Introduction To reduce the mortality rates of patients with sepsis, rapid diagnosis and thera are required. We have therefore discovered the soluble CD14 subtype sCD14!"T#, specific for sepsis and is elevated at an early stage during the disease progres &dditionally, we have been researching a novel fusion protein, '(1))*, which con the modified light chain of interalpha inhibitor and the anti!CD14 antibody as a agent. 6o to: Methods We developed an + -"& using two rat monoclonal antibodies against !terminal and terminal peptide sequences of rabbit sCD14!"T, respectively, to determine sCD14! concentrations in rabbit plasma. "urvival rates and the time course of plasma le sCD14!"T, - !/, and D!dimer were e0amined in a rabbit cecal ligation and punctur model. 2lood bacterial counts were also determined as colony!forming units. 6o to: Results The plasma sCD14!"T levels in seven dead animals clearly increased at 3 hours or together with blood bacterial counts, reached the pea at 5 hours, and then grad decreased at 467 hours, whereas those in one surviving animal did not. The induc was about 34 minutes and the half!life ranged from 4 to 8 hours. &dditionally, t / and D!dimer levels in dead animals clearly increased at 5 hours or later, wher one surviving animal did not. -ntravenous administration of '(1))* with an antib latamo0ef sodium, following the observation of increases in sCD14!"T levels and bacterial counts, improved the survival and the plasma D!dimer levels in a rabb n 9 :, P ; ).)8#. 6o to:

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Presepsin Nakamura 2008 Critical Care

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Crit Care. 2008; 12(Suppl 2): P194.Published online 2008 Mar 13.doi:10.1186/cc6415PMCID:PMC4088565Early elevation of plasma soluble CD14 subtype, a novel biomarker for sepsis, in a rabbit cecal ligation and puncture modelM Nakamura,1T Takeuchi,1K Naito,1K Shirakawa,1Y Hosaka,1F Yamasaki,1andS Furusako1Author informationArticle notesCopyright and License informationGo to:IntroductionTo reduce the mortality rates of patients with sepsis, rapid diagnosis and therapeutic decision are required. We have therefore discovered the soluble CD14 subtype (sCD14-ST), which is specific for sepsis and is elevated at an early stage during the disease progression [1]. Additionally, we have been researching a novel fusion protein, MR1007, which consists of the modified light chain of interalpha inhibitor and the anti-CD14 antibody as an anti-sepsis agent.Go to:MethodsWe developed an ELISA using two rat monoclonal antibodies against N-terminal and C-terminal peptide sequences of rabbit sCD14-ST, respectively, to determine sCD14-ST concentrations in rabbit plasma. Survival rates and the time course of plasma levels of sCD14-ST, IL-6, and D-dimer were examined in a rabbit cecal ligation and puncture (CLP) model. Blood bacterial counts were also determined as colony-forming units.Go to:ResultsThe plasma sCD14-ST levels in seven dead animals clearly increased at 2 hours or later together with blood bacterial counts, reached the peak at 3 hours, and then gradually decreased at 48 hours, whereas those in one surviving animal did not. The induction phase was about 24 minutes and the half-life ranged from 4 to 5 hours. Additionally, the plasma IL-6 and D-dimer levels in dead animals clearly increased at 3 hours or later, whereas those in one surviving animal did not. Intravenous administration of MR1007 with an antibiotic, latamoxef sodium, following the observation of increases in sCD14-ST levels and blood bacterial counts, improved the survival and the plasma D-dimer levels in a rabbit CLP model (n= 9,P< 0.05).Go to:ConclusionPlasma sCD14-ST levels were elevated earlier than IL-6 and D-dimer along with occurrence of blood bacteria in a rabbit CLP model. Therapy with an anti-sepsis agent such as MR1007 following the elevation of sCD14-ST improved the outcome in the CLP model. These results suggest that sCD14-ST is useful to determine the earlier initiation of anti-sepsis therapy.Go to:References1. Yaegashi Y,J Infect Chemother.2005. pp. 234238.[PubMed][Cross Ref]

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