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在大肠杆菌中合成的免疫球蛋白ε链片段对普劳斯尼茨-屈斯特纳反应的抑制作用

Inhibition of the Prausnitz-Küstner reaction by an immunoglobulin epsilon-chain fragment synthesized in E. coli.

作者信息

Geha R S, Helm B, Gould H

出版信息

Nature. 1985;315(6020):577-8. doi: 10.1038/315577a0.

Abstract

The Prausnitz-Küstner (P-K) reaction is a sensitive test for the presence and activity in the skin of immunoglobulin E, an important class of immunoglobulin mediating allergic reactions. A fragment of the human myeloma ND epsilon-chain gene, encoding the second, third and fourth domains of the IgE constant region (C epsilon 2-4) was assessed here for its ability to inhibit the P-K reaction in vivo. Injection of the fragment in skin sites of healthy human adults prevented subsequent sensitization with serum containing IgE antibody to ragweed antigen. Inhibition of the P-K reaction required a 200-fold molar excess of the C epsilon fragment over the IgE present in the sensitizing serum. The efficacy of the C epsilon fragment in inhibiting the P-K reaction compared favourably with that of natural myeloma IgE (PS) in terms of both blocking concentrations and duration of the blocking effect. The inhibition of the P-K reaction by C epsilon 2-4 fragments was specific and probably caused by the saturation of IgE receptors on mast cells by the recombinant gene product.

摘要

普劳斯尼茨-屈斯特纳(P-K)反应是一种用于检测皮肤中免疫球蛋白E(介导过敏反应的一类重要免疫球蛋白)的存在及活性的敏感试验。本文评估了编码IgE恒定区第二、第三和第四结构域(Cε2-4)的人骨髓瘤NDε链基因片段在体内抑制P-K反应的能力。将该片段注射到健康成年人的皮肤部位后,可防止随后用含针对豚草抗原的IgE抗体的血清进行致敏。抑制P-K反应需要Cε片段的摩尔量比致敏血清中存在的IgE过量200倍。就阻断浓度和阻断作用持续时间而言,Cε片段在抑制P-K反应方面的效果与天然骨髓瘤IgE(PS)相比毫不逊色。Cε2-4片段对P-K反应的抑制具有特异性,可能是由重组基因产物使肥大细胞上的IgE受体饱和所致。

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