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BALB/c小鼠中ABPC 48交叉反应性独特型抗原决定簇。天然及果聚糖诱导表达。

ABPC 48 cross-reactive idiotopes in BALB/c mice. Natural and levan-induced expression.

作者信息

Legrain P, Buttin G

出版信息

J Exp Med. 1983 Sep 1;158(3):872-84. doi: 10.1084/jem.158.3.872.

Abstract

Using monoclonal antiidiotypic antibodies, we developed a sensitive binding assay that detects molecules with one or with two idiotopes of the ABPC48 idiotype. ABPC48 cross-reactive idiotypes were thus shown to be present in substantial amounts in sera of nonimmunized mice. Levan binding sites are found on these idiotypes. During the life time of the mice, the natural anti-levan titer increases while ABPC48 idiotypic expression remains constant, suggesting different controls for these two activities. On the other hand, ABPC48 cross-reactive idiotypes participate--as minor components--in the response that follows a deliberate immunization with bacterial levan. This induction process is likely to reflect the selection of idiotopes expressed by the B cell clones preactivated in sera of nonimmunized mice rather than the activation of silent clones. We suggest that a similar situation might explain the reported emergence of ABPC48 idiotypes in animals primed with antiidiotypic antibodies and subsequently stimulated with levan.

摘要

利用单克隆抗独特型抗体,我们开发了一种灵敏的结合测定法,可检测具有ABPC48独特型一个或两个独特位的分子。结果表明,ABPC48交叉反应独特型大量存在于未免疫小鼠的血清中。在这些独特型上发现了左聚糖结合位点。在小鼠的生命周期中,天然抗左聚糖滴度增加,而ABPC48独特型表达保持不变,这表明对这两种活性有不同的调控。另一方面,ABPC48交叉反应独特型作为次要成分参与了用细菌左聚糖进行刻意免疫后产生的反应。这种诱导过程可能反映了对未免疫小鼠血清中预先激活的B细胞克隆所表达独特位的选择,而不是沉默克隆的激活。我们认为,类似的情况可能解释了在用抗独特型抗体致敏并随后用左聚糖刺激的动物中报道的ABPC48独特型的出现。

相似文献

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Regulatory idiotopes, parallel sets and internal image of the antigen within the polyfructosan-A48 idiotypic network.
Ann Immunol (Paris). 1984 Jan-Feb;135C(1):107-15. doi: 10.1016/s0769-2625(84)80019-7.

本文引用的文献

5
Content of a cross-reactive idiotype in nonimmune A/J sera.
Eur J Immunol. 1982 Nov;12(11):977-8. doi: 10.1002/eji.1830121115.
9
Idiotypic regulation in immune networks.免疫网络中的独特型调节
Contemp Top Mol Immunol. 1981;8:113-48. doi: 10.1007/978-1-4684-3917-5_4.

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