Intravenous immunoglobulin attenuates mesenteric ischemia-reperfusion injury

被引:19
作者
Anderson, J
Fleming, SD
Rehrig, S
Tsokos, GC
Basta, M
Shea-Donohue, T
机构
[1] Univ Maryland, Sch Med, Mucosal Biol Res Ctr, Baltimore, MD 21201 USA
[2] Univ Maryland, Dept Med, Baltimore, MD 21201 USA
[3] USDA ARS, Beltsville Human Nutr Res Ctr, Beltsville, MD 20705 USA
[4] NIAID, Clin Invest Lab, NIH, Bethesda, MD 20892 USA
[5] Walter Reed Army Med Ctr, Dept Cellular Injury, Washington, DC 20307 USA
[6] Uniformed Serv Univ Hlth Sci, Dept Med, Bethesda, MD 20814 USA
[7] Uniformed Serv Univ Hlth Sci, Dept Surg, Bethesda, MD 20814 USA
[8] MD Inst Res, Dept Surg, Walter Reed Army Forest Glen, Silver Spring, MD 20910 USA
关键词
complement; IVIG; ischemia-reperfusion; neutrophil; inflammation; rat;
D O I
10.1016/j.clim.2004.08.018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Intravenous immunoglobulin (IVIG) has been found useful in the treatment of various clinical entities and its effect has been associated with inhibition of complement-mediated tissue damage. The aim of this study was to determine the ability of IVIG to protect against mesenteric ischemia-reperfusion (IR)-induced local and remote injury. Rats received vehicle or IVIG (150-600 mg/kg) 5 min prior to sham operation or 30 min of superior mesenteric artery occlusion, followed by 5, 120, or 240 min of reperfusion. IVIG reduced IR-induced mucosal injury without altering IR-induced increases in PMN infiltration or LTB4 generation. At 5 min post IR, the deposition of IgG and C3 in the lamina propria and surface epithelial cells was attenuated by IVIG. The increased capillary leak, evident at 240 min, was inhibited by IVIG and coincided with a reduction in C3 deposition in lung tissue. The beneficial effects of IVIG may be related to the ability to scavenge deleterious products. Published by Elsevier Inc.
引用
收藏
页码:137 / 146
页数:10
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