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1.
J Intern Med ; 274(4): 381-90, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23808943

ABSTRACT

BACKGROUND: More than 500,000 hospitalized patients survive severe sepsis annually in the USA. Recent epidemiological evidence, however, demonstrated that these survivors have significant morbidity and mortality, with 3-year fatality rates higher than 70%. To investigate the mechanisms underlying persistent functional impairment in sepsis survivors, here we developed a model to study severe sepsis survivors following cecal ligation and puncture (CLP). METHODS: Sepsis was induced in mice by CLP and survivors were followed for twelve weeks. Spleen and blood were collected and analyzed at different time points post-sepsis. RESULTS: We observed that sepsis survivors developed significant splenomegaly. Analysis of the splenic cellular compartments revealed a major expansion of the inflammatory CD11b+ Ly-6CHigh pool. Serum high-mobility group box 1 (HMGB1) levels in the sepsis surviving mice were significantly elevated for 4-6 weeks after post-sepsis, and administration of an anti-HMGB1 monoclonal antibody significantly attenuated splenomegaly as well as splenocyte priming. Administration of recombinant HMGB1 to naive mice induced similar splenomegaly, leukocytosis and splenocyte priming as observed in sepsis survivors. Interestingly analysis of circulating HMGB1 from sepsis survivors by mass spectroscopy demonstrated a stepwise increase of reduced form of HMGB1 (with known chemo-attractant properties) during the first 3 weeks, followed by disulphide form (with known inflammatory properties) 4-8 weeks after CLP. DISCUSSION: Our results indicate that prolonged elevation of HMGB1 is a necessary and sufficient mediator of splenomegaly and splenocyte expansion, as well as splenocyte inflammatory priming in murine severe sepsis survivors.


Subject(s)
Antigens, Ly/immunology , Bacteremia/immunology , CD11b Antigen/immunology , HMGB1 Protein/physiology , Monocytes/immunology , Splenomegaly/immunology , Animals , Cecum/injuries , Disease Models, Animal , Humans , Inflammation/immunology , Ligation , Male , Mice , Mice, Inbred BALB C , Punctures/adverse effects , Spleen/immunology
2.
Adv Colloid Interface Sci ; 123-126: 425-31, 2006 Nov 16.
Article in English | MEDLINE | ID: mdl-16860284

ABSTRACT

The synthesis and study of oil-soluble metal carbonate colloids are of interest in the area of lubricant additives. These surfactant-stabilised nanoparticles are important components in marine and automotive engine oils. Recently introduced, environmentally driven legislation has focused on lowering of gaseous emissions by placing limits on the levels of phosphorous sulphur and ash allowed in engine oil systems. These chemical limits, coupled with improved engine performance and extended oil drainage intervals, have lead to renewed interest in the production of stable, efficient nanodetergent systems. To date, this has resulted in modification of existing surfactant structures and development of new generations of surfactants. This review covers the current state of research in the area of nanodetergents.

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