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用针对广谱脂多糖反应性抗体 WN1 222-5 的抗独特型抗体免疫接种可诱导家兔产生大肠杆菌 R3-核心型特异性抗体。

Immunization with an anti-idiotypic antibody against the broadly lipopolysaccharide-reactive antibody WN1 222-5 induces Escherichia coli R3-core-type specific antibodies in rabbits.

机构信息

Research Center Borstel, Leibniz-Center for Medicine and Biosciences, Borstel, Germany.

出版信息

Innate Immun. 2012 Apr;18(2):279-93. doi: 10.1177/1753425911401055. Epub 2011 Aug 15.

Abstract

The mouse monoclonal antibody (mAb) WN1 222-5 recognizes a carbohydrate epitope in the inner core region of LPS that is shared by all strains of Escherichia coli and Salmonella enterica and is able to neutralize their endotoxic activity in vitro and in vivo. Immunization of mice with mAb WN1 222-5 yielded several anti-idiotypic mAbs one of which (mAb S81-19) competitively inhibited binding of mAb WN1 222-5 to E. coli and Salmonella LPS. After immunization of rabbits with mAb S81-19, the serological responses towards LPS were characterized at intervals over two years. Whereas the serological response against the anti-idiotype developed as expected, the anti-anti-idiotypic response against LPS developed slowly and antibodies appeared after 200 d that bound to E. coli LPS of the R3 core-type and neutralized its TNF-α inducing capacity for human peripheral mononuclear cells. We describe the generation of a novel anti-idiotypic antibody that can induce LPS core-reactive antibodies upon immunization in rabbits and show that it is possible, in principle, to obtain LPS neutralizing antibodies by anti-idiotypic immunization against the mAb WN1 222-5. The mimicked epitope likely shares common determinants with the WN1 222-5 epitope, yet differences with respect to either affinity or specificity do exist, as binding to smaller oligosaccharides of the inner core was not observed.

摘要

鼠源单克隆抗体(mAb)WN1 222-5 识别 LPS 核心内部区域的碳水化合物表位,该表位存在于所有大肠杆菌和沙门氏菌血清型中,能够中和其在体外和体内的内毒素活性。用 mAb WN1 222-5 免疫小鼠可产生几种抗独特型 mAb,其中一种(mAb S81-19)竞争性抑制 mAb WN1 222-5 与大肠杆菌和沙门氏菌 LPS 的结合。用 mAb S81-19 免疫兔后,在两年多的时间里每隔一段时间就对 LPS 的血清学反应进行了特征描述。尽管针对抗独特型的血清学反应如预期的那样发展,但针对 LPS 的抗抗独特型反应发展缓慢,在 200 天后才出现与 R3 核心型大肠杆菌 LPS 结合并中和其对人外周单核细胞 TNF-α诱导能力的抗体。我们描述了一种新型抗独特型抗体的产生,该抗体在兔中免疫后可诱导 LPS 核心反应性抗体,并表明通过针对 mAb WN1 222-5 的抗独特型免疫,获得 LPS 中和抗体在原则上是可行的。模拟表位可能与 WN1 222-5 表位具有共同决定簇,但在亲和力或特异性方面存在差异,因为没有观察到与较小的内核心寡糖结合。

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