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At low serum glucan concentrations there is an inverse correlation between serum glucan and serum cytokine levels in ICU patients with infections
被引:4
|作者:
Gonzalez, JA
Digby, JD
Rice, PJ
Breuel, KF
DePonti, WK
Kalbfleisch, JH
Browder, IW
Williams, DL
[1
]
机构:
[1] E Tennessee State Univ, James H Quillen Coll Med, Dept Surg, Johnson City, TN 37614 USA
[2] E Tennessee State Univ, James H Quillen Coll Med, Dept Pharmacol, Johnson City, TN 37614 USA
[3] E Tennessee State Univ, James H Quillen Coll Med, Dept Obstet & Gynecol, Johnson City, TN 37614 USA
[4] E Tennessee State Univ, James H Quillen Coll Med, Dept Med Comp & Biometry, Johnson City, TN 37614 USA
关键词:
glucan;
cytokines;
infection;
serum;
D O I:
10.1016/j.intimp.2004.05.010
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Glucans are fungal cell wall glucose polymers that are released into the blood of infected patients. The role of glucans in infection is unknown. We examined serum glucan and cytokine levels in intensive care unit (ICU) patients with infections. There was an inverse correlation (p<0.001) between serum glucan levels and interleukin (IL)-2), IL-4, tumor necrosis factoralpha (TNFalpha) and granulocyte macrophage-colony stimulating factor (GM-CSF) levels in infected ICU patients. The correlation between serum cytokines and serum glucan was only observed at glucan concentrations < 40 pg/ml. No change was observed at serum glucan levels of >40 pg/ml. There was no correlation between serum glucan levels and systemic levels of IL-1beta, IL-5, IL-6, IL-8, IL-10 or IFN-gamma. Interestingly, blood home glucans did not suppress systemic cytokine levels in infected ICU patients, instead they were maintained at control levels. We conclude that circulating glucans may prevent cytokine upregulation in response to infection. This may represent an adaptive response to septic injury. (C) 2004 Elsevier B.V. All rights reserved.
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页码:1107 / 1115
页数:9
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