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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/32115
Title: Endogenous α<inf>2</inf>-antiplasmin is protective during severe gram-negative sepsis (Melioidosis)
Authors: Liesbeth M. Kager
Tassili A. Weehuizen
W. Joost Wiersinga
Joris J.T.H. Roelofs
Joost C.M. Meijers
Arjen M. Dondorp
Cornelis Van't Veer
Tom Van Der Poll
Academic Medical Centre, University of Amsterdam
University of Amsterdam
Mahidol University
John Radcliffe Hospital
Keywords: Medicine
Issue Date: 15-Oct-2013
Citation: American Journal of Respiratory and Critical Care Medicine. Vol.188, No.8 (2013), 967-975
Abstract: Rationale: α2-Antiplasmin (A2AP) is a major inhibitor of fibrinolysis by virtue of its capacity to inhibit plasmin. Although the fibrinolytic system is strongly affected by infection, the functional role of A2AP in the host response to sepsis is unknown. Objectives: To study the role of A2AP in melioidosis, a common form ofcommunity-acquired sepsis in SoutheastAsia and Northern Australia caused by the gram-negative bacterium Burkholderia pseudomallei. Methods: In a single-center observational study A2AP was measured in patients with culture-proven septic melioidosis. Wild-type and A2AP-deficient (A2AP-/-) mice were intranasally infected with B. pseudomallei to induce severe pneumosepsis (melioidosis). Parameters of inflammation and coagulation were measured, and survival studies were performed. Measurements and Main Results: Patients with melioidosis showed elevated A2AP plasma levels. Likewise, A2AP levels in plasma and lunghomogenates were elevated in mice infected with B. pseudomallei. A2AP-deficient (A2AP-/-) mice had a strongly disturbed host response during experimental melioidosis as reflected by enhanced bacterial growth at the primary site of infection accompanied by increased dissemination to distant organs. In addition, A2AP-/- mice showed more severe lung pathology and injury together with an increased accumulation of neutrophils and higher cytokine levels in lung tissue. A2AP deficiency further was associated with exaggerated systemic inflammation and coagulation, increased distant organ injury, and enhanced lethality. Conclusions: This study is the first to identify A2AP as a protective mediator during gram-negative (pneumo)sepsis by limiting bacterial growth, inflammation, tissue injury, and coagulation. Copyright © 2013 by the American Thoracic Society.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84886381344&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/32115
ISSN: 15354970
1073449X
Appears in Collections:Scopus 2011-2015

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