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健康人和菌血症患者对肠杆菌外膜蛋白特定结构域的抗体反应。

Antibody response to defined domains on enterobacterial outer membrane proteins in healthy persons and patients with bacteraemia.

作者信息

Henriksen A Z, Maeland J A

机构信息

Department of Microbiology, Faculty of Medicine, University of Trondheim, Norway.

出版信息

APMIS. 1990 Feb;98(2):163-72. doi: 10.1111/j.1699-0463.1990.tb01017.x.

Abstract

Monoclonal antibody (MAb)-based competitive enzyme immunoassays (cELISAs) were elaborated to measure antibodies against MAb-defined domains on three different enterobacterial outer membrane (OM) proteins in sera from healthy individuals (n = 30) and in paired serum samples from patients (n = 45) with bacteraemia caused by enterobacteria or by various nonenteric bacteria (n = 15). The MAb-defined domains were Hm I and Hm II on the heat-modifiable (Hm) protein, PALp I and PALp II on the peptidoglycan-associated lipoprotein (PALp), and BLp I on Braun's lipoprotein (BLp). All MAbs have shown broad cross-reactivity with and specificity for enterobacteria. Sera from healthy individuals and from patients with infections caused by nonenteric bacteria contained low levels of MAb-blocking antibodies. Bacteraemia caused by enterobacteria resulted in generation of antibodies against the MAb-defined domains in many of the patients. Thus, 40% and 69% showed a positive BLp I cELISA with the first and second serum samples, respectively. Of the second serum samples, 20-38% showed positive Hm and PALp cELISAs. The BLp I cELISA showed higher diagnostic sensitivity than the previously described indirect ELISA for IgG antibodies against E. coli 055 OM protein antigens. Assays using the MAbs as competitors showed that the patients bacteraemic with enterobacteria, also generated antibodies against other domains on the OM proteins. The cELISAs may be useful in the diagnosis and management of patients with serious infections caused by enterobacteria. In this regard, the BLp I cELISA showed the most promising results.

摘要

构建了基于单克隆抗体(MAb)的竞争性酶免疫测定法(cELISA),以检测健康个体(n = 30)血清以及由肠杆菌或各种非肠道细菌引起菌血症的患者(n = 45)配对血清样本中,针对三种不同肠杆菌外膜(OM)蛋白上MAb定义结构域的抗体。MAb定义的结构域分别是热修饰(Hm)蛋白上的Hm I和Hm II、肽聚糖相关脂蛋白(PALp)上的PALp I和PALp II,以及布劳恩脂蛋白(BLp)上的BLp I。所有MAb均显示出与肠杆菌具有广泛的交叉反应性和特异性。健康个体以及由非肠道细菌引起感染患者的血清中,MAb阻断抗体水平较低。肠杆菌引起的菌血症导致许多患者产生针对MAb定义结构域的抗体。因此,分别有40%和69%的患者第一份和第二份血清样本的BLp I cELISA呈阳性。在第二份血清样本中,20 - 38%的样本Hm和PALp cELISA呈阳性。与先前描述的针对大肠杆菌055 OM蛋白抗原的IgG抗体间接ELISA相比,BLp I cELISA显示出更高的诊断敏感性。使用MAb作为竞争剂的测定表明,患有肠杆菌菌血症的患者还产生了针对OM蛋白上其他结构域的抗体。cELISA可能有助于诊断和管理由肠杆菌引起严重感染的患者。在这方面,BLp I cELISA显示出最有前景的结果。

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