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通过在草花粉过敏患者中使用抗独特型诱导的组胺释放来证明嗜碱性粒细胞结合的IgE抗体上表达的独特型。

Demonstration of idiotypes expressed on basophil-bound IgE antibodies by using anti-idiotype-induced histamine release in grass pollen-allergic patients.

作者信息

Mecheri S, Mourad W, Lapeyre J, Jobin M, David B, Hébert J

机构信息

Unité d'Immuno-Allergie, Institut Pasteur, Paris, France.

出版信息

Immunology. 1988 May;64(1):11-5.

Abstract

This study was designed to analyse further the idiotypic cross-reactivity between anti-Lol p I murine monoclonal antibodies of IgG isotype and basophil-bound human IgE antibodies from grass pollen-sensitive patients. It was also designed to determine the expression frequency of the idiotypes present on cell-bound IgE. Rabbit anti-idiotypic antisera were produced against idiotypes of three anti-Lol p I monoclonal antibodies (290A-167, 539A-6 and 348A-6) of different specificities. Basophils from 19 patients reacting to Lol p I allergen, as shown by positive skin test reactions and by the presence of serum-specific IgE antibodies (measured by RAST), were challenged with these rabbit anti-idiotypic antibodies and the histamine released was measured. Our data indicate that IgE-borne idiotypes were expressed as follows: (i) co-expression of the three idiotypes in 15% of patients; (ii) co-expression of two idiotypes in 21% of patients; and (iii) expression of a unique idiotype (290A-167) in 42% of patients. Among the three idiotypes, 290A-167 was shown to be a public idiotype since it was expressed in 80% of patients. Fab fragments of anti-idiotypic antibodies could inhibit anti-idiotype-induced histamine release, but optimal conditions varied from one patient to another.

摘要

本研究旨在进一步分析IgG同种型的抗变应原Lol p I小鼠单克隆抗体与草花粉敏感患者嗜碱性粒细胞结合的人IgE抗体之间的独特型交叉反应性。本研究还旨在确定细胞结合型IgE上存在的独特型的表达频率。针对三种不同特异性的抗变应原Lol p I单克隆抗体(290A - 167、539A - 6和348A - 6)的独特型制备了兔抗独特型抗血清。19例对变应原Lol p I有反应的患者的嗜碱性粒细胞,通过阳性皮肤试验反应和血清特异性IgE抗体的存在(通过放射性变应原吸附试验测定)表明,用这些兔抗独特型抗体进行攻击,并测量释放的组胺。我们的数据表明,IgE携带的独特型表达如下:(i)15%的患者中三种独特型共表达;(ii)21%的患者中两种独特型共表达;(iii)42%的患者中表达一种独特型(290A - 167)。在这三种独特型中,290A - 167被证明是一种公共独特型,因为它在80%的患者中表达。抗独特型抗体的Fab片段可以抑制抗独特型诱导的组胺释放,但最佳条件因患者而异。

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