Thymosin β4 reduces lethality and down-regulates inflammatory mediators in endotoxin-induced septic shock

被引:111
作者
Badamchian, M
Fagarasan, MO
Danner, RL
Suffredini, AF
Damavandy, H
Goldstein, AL
机构
[1] George Washington Univ, Sch Med & Hlth Sci, Dept Biochem & Mol Biol, Washington, DC 20037 USA
[2] NIH, Warren G Magnuson Clin Ctr, Dept Crit Care Med, Bethesda, MD 20892 USA
关键词
thymosin beta(4); septic shock; LPS; endotoxin;
D O I
10.1016/S1567-5769(03)00024-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thymosin beta(4) (Tbeta(4), a highly conserved peptide with immunomodulatory properties, is the major actin-sequestering peptide in mammalian cells. Recent studies have established that Tbeta(4) can accelerate wound healing in full thickness skin wounds and following burn injuries to the cornea. In the eye studies, the accelerated healing due to Tbeta(4) was accompanied by a significant reduction in polymorphonuclear leukocyte (PMN) infiltration and a several-fold decrease in interleukin-1beta (p less than or equal to 0.015) and 6-keto-prostaglandin F-1alpha (6-keto-PGF(1alpha), p less than or equal to 0.05). Given the recognized role of proinflammatory cytokines in septic shock and of extracellular F- and G-actin in the pathophysiology of multiple organ dysfunction, we have investigated the role of Tbeta(4) in sepsis. We report that an LD50 dose of LPS (24 mg/kg) in rats resulted in a significant reduction of Tbeta(4) levels in the blood. Furthermore, administration of 100 mug of Tbeta(4) immediately following and at 2 and 4 It after an LD50 dose of LPS (60 mg/kg) in mice significantly reduced mortality rates (p less than or equal to 0.024) and lowered blood levels of a number of inflammatory cytokines, eicosanoids. and other molecules that are highly elevated following endotoxin administration. In studies in human subjects given low doses of endotoxin (4 ng/kg LPS) and in patients with septic shock, we have also observed significant decreases in blood levels of Tbeta(4). The rapid disappearance of Tbeta(4) in the blood following LPS administration or during septic shock suggests that Tbeta(4) may be involved in early events leading to activation of the inflammatory cascade and ultimately the clinical sequelae of sepsis. The results of this study indicate that Tbeta(4) may have utility in the clinic in the treatment of septic shock and in syndromes associated with actin toxicities. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1225 / 1233
页数:9
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