首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Protection against the staphylococcal enterotoxin-induced intestinal disorder in the monkey by anti-idiotypic antibodies.
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Protection against the staphylococcal enterotoxin-induced intestinal disorder in the monkey by anti-idiotypic antibodies.

机译:抗独特型抗体可保护猴子预防由葡萄球菌肠毒素引起的肠道疾病。

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摘要

The staphylococcal enterotoxin serotype B (SEB)-induced enteric intoxication and the immediate-type reaction in the skin of unsensitized monkeys was used to define whether agents competing with SEB for target cell receptors may inhibit pathophysiological effects. For this purpose a duodenal provocation test was developed by use of a pediatric gastroscope, allowing the evaluation of the influence of antagonists on the intestinal disorder upon SEB challenge at the same duodenal site. First, carboxymethylation of histidine residues of SEB caused a complete loss of emetic and skin-sensitizing activity without changing the immunological specificity. However, carboxymethylated SEB is a strong inhibitor of enteric intoxications and immediate-type skin reactions upon SEB challenge. Second, after immunization of BALB/c mice with monoclonal anti-SEB antibodies, monoclonal antiidiotypic antibodies (anti-Id) were obtained by the "hybridoma technique" and purification by idiotype-affinity chromatography. Anti-Id specifically inhibited the binding of horseradish peroxidase-labeled anti-SEB to the ligand, and SEB blocked as well the interaction of these two antibody species, indicating a high degree of binding-site selectivity. Anti-Id completely protected against emetic response and diarrhea upon duodenal provocation with SEB and inhibited immediate-type skin reactions as well. Further, anti-Id acted as an antagonist without triggering biologic functions themselves. This shows that anti-Id constitute a useful tool to protect against a bacterial toxin-induced intestinal disorder.
机译:葡萄球菌肠毒素血清型B(SEB)引起的肠中毒和未致敏猴子皮肤中的立即型反应用于确定与SEB竞争靶细胞受体的药物是否可以抑制病理生理作用。为了这个目的,通过使用小儿胃镜开发了十二指肠激发试验,以评估在相同的十二指肠部位上SEB攻击时拮抗剂对肠道疾病的影响。首先,SEB组氨酸残基的羧甲基化导致呕吐和皮肤敏化活性完全丧失,而没有改变免疫学特异性。但是,羧甲基化SEB是SEB激发后肠中毒和速发型皮肤反应的强力抑制剂。第二,用单克隆抗SEB抗体免疫BALB / c小鼠后,通过“杂交瘤技术”获得单克隆抗独特型抗体(抗-Id),并通过独特型亲和层析纯化。抗-Id特异性抑制辣根过氧化物酶标记的抗-SEB与配体的结合,SEB也阻止了这两种抗体种类的相互作用,表明高度的结合位点选择性。抗-Id完全防止SEB引起十二指肠刺激引起的催吐反应和腹泻,并且还抑制速发型皮肤反应。此外,抗-Id充当拮抗剂而不自身触发生物学功能。这表明抗-Id构成了防止细菌毒素诱导的肠道疾病的有用工具。

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