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Relationship between a low toxicity of the mutant A subunit of enterotoxigenic Escherichia coli enterotoxin and its strong adjuvant action.

机译:产肠毒素大肠杆菌肠毒素的突变体A亚基的低毒性与其强大的佐剂作用之间的关系。

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摘要

In the work described here it was determined if and how unnicking in the A subunit of Escherichia coli enterotoxin at Arg192 or nearby residues affected biological activities of the toxin. The mutant toxin was constructed to lack the nick site in the A subunit by deleting the tripeptide Arg192-Thr193-Ile194, which is essential for toxicity. The mutant toxin did not exhibit agmatine ADP-ribosyltransferase activity in the presence or absence of the ADP-ribosylation factor and had less diarrhoeal activity and lower induction of cyclic AMP than did LT. The mutant toxin exhibited a much stronger adjuvant action on antibody responses to measles virus, keyhole limpt haemocyanin, bovine immunoglobulin and ovalbumin compared with LT. The altered toxicity of the mutant toxin might be closely related to the potent adjuvant action on antibody responses to antigens. The relationship between two activities is discussed.
机译:在这里描述的工作中,确定了大肠杆菌肠毒素的A亚基在Arg192处或附近残基的去切口是否以及如何影响该毒素的生物活性。通过删除对毒性必不可少的三肽Arg192-Thr193-Ile194,构建了突变毒素,使其在A亚基中缺少缺口位点。在存在或不存在ADP-核糖基化因子的情况下,与LT相比,突变毒素不显示出胍丁胺ADP-核糖基转移酶活性,并且腹泻活性和对环AMP的诱导作用更低。与LT相比,突变毒素对麻疹病毒,匙孔lim血红蛋白,牛免疫球蛋白和卵清蛋白的抗体反应表现出更强的佐剂作用。突变毒素毒性的改变可能与针对抗原的抗体应答的有效佐剂作用密切相关。讨论了两个活动之间的关系。

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