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抗对氨基苯砷酸抗体应答中抗交叉反应性独特型单克隆抗体诱导的独特型抑制研究。

Study of idiotopic suppression induced by anti-cross-reactive idiotype monoclonal antibody in the anti-p-azophenylarsonate antibody response.

作者信息

Hiernaux J R, Marvel J, Meyers P, Moser M, Leo O, Slaoui M, Urbain J

出版信息

J Immunol. 1986 Mar 15;136(6):1960-7.

PMID:3950406
Abstract

A/J mice immunized with p-azophenylarsonate coupled to keyhole limpet hemocyanin produce antibodies expressing a cross-reactive idiotype (CRIA). The pretreatment of A/J mice with anti-idiotypic polyclonal or monoclonal antibody directed against the major cross-reactive idiotype (CRIA) borne by p-azophenylarsonate-specific antibody can lead to idiotypic suppression. In this study, we investigate this idiotypic suppression by using four mAb2 (E4, H8, E3, 2D3) recognizing distinct idiotopes whose expression is related to the presence of particular gene segments of the heavy chain V region. 2D3 expression has been related to the presence of some amino acid in the CDR2 region of the VH gene segment derived from the germ line VH IdCR11. So far, the latter is the only germ-line gene coding for CRIA+ antibody that has been identified in the A/J genome. E4 and H8 expression has been related to the use of a particular D segment, whereas E3 expression has been attributed to certain combinations of D and JH segments. Therefore, we might expect independent regulation of the expression of those various idiotopes in relation to the mechanism of gene recombination. Indeed, we observed that 2D3-suppressed A/J mice still produce the three other idiotopes, suggesting the recombination of those particular D and J segments with a different VH gene. Such a gene has been identified in the genome of BALB/c mice. A/J mice pretreated with one of the other three mAb2 are generally cosuppressed for the expression of E4, H8, and E3, but they still produce 2D3+ antibody. In this case, the IdCR11 VH germ-line gene is most probably recombined with different D and J segments. Molecular evidence for the existence of such molecules has also been presented in the literature. So our serologic data on idiotopic suppression in the arsonate system can be compared with recent data provided by molecular genetics.

摘要

用对氨基苯胂酸偶联的钥孔戚血蓝蛋白免疫的A/J小鼠产生表达交叉反应独特型(CRIA)的抗体。用针对对氨基苯胂酸特异性抗体所携带的主要交叉反应独特型(CRIA)的抗独特型多克隆或单克隆抗体预处理A/J小鼠可导致独特型抑制。在本研究中,我们使用四种识别不同独特位的单克隆抗体2(E4、H8、E3、2D3)来研究这种独特型抑制,这些独特位的表达与重链V区特定基因片段的存在有关。2D3的表达与源自种系VH IdCR11的VH基因片段的互补决定区2(CDR2)区域中某些氨基酸的存在有关。到目前为止,后者是在A/J基因组中已鉴定出的唯一编码CRIA+抗体的种系基因。E4和H8的表达与特定D片段的使用有关,而E3的表达归因于D和JH片段的某些组合。因此,我们可能预期这些不同独特位的表达会相对于基因重组机制受到独立调控。实际上,我们观察到2D3抑制的A/J小鼠仍产生其他三种独特位,这表明那些特定的D和J片段与不同的VH基因发生了重组。这样的基因已在BALB/c小鼠的基因组中被鉴定出来。用其他三种单克隆抗体2之一预处理的A/J小鼠通常对E4、H8和E3的表达产生共抑制,但它们仍产生2D3+抗体。在这种情况下,IdCR11 VH种系基因很可能与不同的D和J片段发生了重组。文献中也已提供了此类分子存在的分子证据。因此,我们关于胂酸盐系统中独特型抑制的血清学数据可与分子遗传学提供的最新数据进行比较。

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