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针对大肠杆菌脂多糖O多糖和核心区域的单克隆抗体在犬脓毒症休克中的不同功能活性。

Distinct functional activities in canine septic shock of monoclonal antibodies specific for the O polysaccharide and core regions of Escherichia coli lipopolysaccharide.

作者信息

Hoffman W D, Pollack M, Banks S M, Koev L A, Solomon M A, Danner R L, Koles N, Guelde G, Yatsiv I, Mouginis T

机构信息

Critical Care Medicine Department, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Infect Dis. 1994 Mar;169(3):553-61. doi: 10.1093/infdis/169.3.553.

Abstract

Monoclonal antibodies (MAbs) specific for O polysaccharide or core oligosaccharide/lipid A of Escherichia coli O111:B4 lipopolysaccharide (LPS) were compared in canine septic shock. Animals received O-specific, core-specific, or control murine IgG2a MAbs (or saline) before intraperitoneal implantation of an E. coli O111:B4-infected clot. Animals were further randomized to ceftriaxone or saline. O-specific MAb significantly reduced bacteremia and endotoxemia but not serum tumor necrosis factor. Core-specific MAb significantly increased mean arterial pressure from day 4 to 28 (P = .02). In dogs not receiving ceftriaxone, survival was enhanced by O-specific MAb (4/5) compared with core-specific MAb (0/5) and control (1/8) (P = .03). Survival rates were similar (P = .22) but survival was prolonged in antibiotic-treated animals also receiving O-specific MAb (P = .02 vs. core-specific MAb and controls) or core-specific MAb (P = .08 vs. controls). These data support the complex role of LPS in sepsis and the discrete functional effects of MAbs specific for different elements of LPS.

摘要

在犬类脓毒症休克模型中,对针对大肠杆菌O111:B4脂多糖(LPS)的O多糖或核心寡糖/脂质A的单克隆抗体(MAb)进行了比较。在腹腔植入感染大肠杆菌O111:B4的血凝块之前,动物接受O特异性、核心特异性或对照鼠IgG2a单克隆抗体(或生理盐水)。动物进一步随机分为接受头孢曲松或生理盐水组。O特异性单克隆抗体显著降低了菌血症和内毒素血症,但未降低血清肿瘤坏死因子水平。核心特异性单克隆抗体从第4天到28天显著提高了平均动脉压(P = 0.02)。在未接受头孢曲松的犬类中,与核心特异性单克隆抗体组(0/5)和对照组(1/8)相比,O特异性单克隆抗体提高了生存率(4/5)(P = 0.03)。在接受抗生素治疗的动物中,同时接受O特异性单克隆抗体(与核心特异性单克隆抗体组和对照组相比,P = 0.02)或核心特异性单克隆抗体(与对照组相比,P = 0.08)的动物生存率相似(P = 0.22),但生存时间延长。这些数据支持了LPS在脓毒症中的复杂作用以及针对LPS不同成分的单克隆抗体的离散功能效应。

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