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Journal of Southern Medical University ; (12): 544-547, 2016.
Artículo en Chino | WPRIM | ID: wpr-264007

RESUMEN

<p><b>OBJECTIVE</b>To investigate the correlation of the changes in CD8(+)CD28(-) T cell percentage with platelet (PLT) and D-dimer (D-D) levels in patients with multiple injuries (MI).</p><p><b>METHODS</b>Twenty-six patients with MI, 31 with a single injury (SI group) and 26 healthy individuals were examined for peripheral blood CD8(+)CD28(-) T cells and intracellular transformation growth factor-β1 (TGF-β1) and interleukin 10 (IL-10) contents using flow cytometry at 24, 48, and 72 h after the injuries. PLT and D-dimer levels were compared among the 3 groups.</p><p><b>RESULTS</b>CD8(+)CD28(-) T cells, TGF-β1 and IL-10 were significantly higher in MI group than in SI group and healthy control group (P<0.05) without significant differences between the latter 2 groups. The levels of PLT and D-D differed significantly among the 3 groups, the highest in MI group and the lowest in the control group. In MI group, CD8(+)CD28(-) T cells, TGF-β1 and IL-10 significantly increased at 48 h after the injury (P<0.05) but decreased significantly at 72 h (P<0.05) compared with the measurements at 24 h. The levels of PLT and D-D trended to decrease with time after the injuries and showed significant differences among the 3 groups at any of the 3 time points (P<0.05). CD8(+)CD28(-) T cells, TGF-β1 and IL-10 were all positively correlated with the levels of PLT and D-D in MI patients (r>0.70, P<0.05 for all comparisons).</p><p><b>CONCLUSION</b>In MI patients, CD8(+)CD28(-) T cell percentage and their cytokines tend to increase early after the injury but decrease significantly at 72 h in close relation with the changes of the coagulation function following the injuries.</p>


Asunto(s)
Humanos , Antígenos CD28 , Metabolismo , Antígenos CD8 , Metabolismo , Estudios de Casos y Controles , Productos de Degradación de Fibrina-Fibrinógeno , Metabolismo , Citometría de Flujo , Interleucina-10 , Metabolismo , Traumatismo Múltiple , Alergia e Inmunología , Subgrupos de Linfocitos T , Biología Celular , Factor de Crecimiento Transformador beta1 , Metabolismo
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