首页   按字顺浏览 期刊浏览 卷期浏览 Effects of Trauma and Sepsis on Soluble L-Selectin and Cell Surface Expression of L-Sel...
Effects of Trauma and Sepsis on Soluble L-Selectin and Cell Surface Expression of L-Selectin and CD11b

 

作者: K. Maekawa,   S. Futami,   M. Nishida,   T. Terada,   H. Inagawa,   S. Suzuki,   K. Ono,  

 

期刊: The Journal of Trauma: Injury, Infection, and Critical Care  (OVID Available online 1998)
卷期: Volume 44, issue 3  

页码: 460-468

 

ISSN:0022-5282

 

年代: 1998

 

出版商: OVID

 

数据来源: OVID

 

摘要:

ObjectivesTo examine (1) the effects of trauma on changes in neutrophil L-selectin and CD11b expression and on the levels of soluble L-selectin and (2) whether these alterations are different on leukocyte subpopulations in those patients who develop multiple organ dysfunction syndrome.Materials and Methodsor=to 16 and 15 patients with ISS score < 16 were studied. Arterial blood were collected serially after injury. The staining of leukocyte surface adhesion molecules was performed with antibodies against L-selectin and CD11b. Positive cell count and mean fluorescence intensity were determined by flow cytometry. Soluble L-selectin was measured using enzyme-linked immunosorbent assay.Resultsor=to 16, neutrophil L-selectin expression showed an immediate increase, reaching peak levels between 3 to 4 hours after injury (p < 0.05 vs. patients with ISS < 16), followed by a gradual decrease. Plasma levels of soluble L-selectin reached peak levels at 6 hours after injury. However, in patients with ISS < 16, minimal changes in L-selectin expression and soluble L-selectin were observed. Neutrophil CD11b expression showed an immediate increase for the first 3 hours followed by a gradual increase up to 24 hours after injury. In patients who developed multiple organ dysfunction syndrome, CD11b both on neutrophils and lymphocytes remained elevated for 120 hours.ConclusionsThese findings suggest that acute neutrophil activation is an early event after trauma and may be implicated as "a vulnerable window" for leukocyte-mediated end organ injury.

 



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