Thomas J W
Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232.
Eur J Immunol. 1992 Sep;22(9):2445-8. doi: 10.1002/eji.1830220938.
In humans and in BALB/c mice, immune responses to the hormone insulin use evolutionarily related VHV (human) and VHIX (murine) gene families. To determine if these structural relationships include regulatory elements, BALB/c mice were pretreated with autologous immunoglobulin G (IgG) monoclonal antibodies (mAb) that recognize shared idiotopes on human anti-insulin antibodies and the subsequent immune response to human insulin assessed. One mAb, Id227, was found to augment and accelerate the insulin response by inducing a human idiotype that is expressed on both insulin-binding and non-insulin-binding BALB/c antibodies. Analysis of VH gene utilization by Id227 shows that it expresses a VHIX gene similar to that of anti-insulin mAb 125, but the anti-Id has no anti-insulin activity. Using DNA amplification, four germ-line VHIX genes were isolated from BALB/c liver DNA and sequence analysis shows that the anti-insulin and anti-Id are derived from the same germ-line gene. Consistent with its role as a regulatory idiotype, IgG Id227 entirely preserves germ-line sequence in the complementary determining regions and contains only three mutations in framework regions. These studies show that both structural and regulatory features of immune responses to conserved self antigens extend beyond species boundaries.
在人类和BALB/c小鼠中,对激素胰岛素的免疫反应使用进化相关的VHV(人类)和VHIX(小鼠)基因家族。为了确定这些结构关系是否包括调控元件,用识别人类抗胰岛素抗体上共享独特型的自体免疫球蛋白G(IgG)单克隆抗体(mAb)预处理BALB/c小鼠,并评估随后对人类胰岛素的免疫反应。发现一种单克隆抗体Id227通过诱导在胰岛素结合和非胰岛素结合的BALB/c抗体上均表达的人类独特型来增强和加速胰岛素反应。对Id227的VH基因利用情况分析表明,它表达一种与抗胰岛素单克隆抗体125相似的VHIX基因,但抗独特型抗体没有抗胰岛素活性。通过DNA扩增,从BALB/c肝脏DNA中分离出四个种系VHIX基因,序列分析表明抗胰岛素抗体和抗独特型抗体源自同一个种系基因。与其作为调控独特型的作用一致,IgG Id227在互补决定区完全保留种系序列,在框架区仅含有三个突变。这些研究表明,对保守自身抗原的免疫反应的结构和调控特征均跨越物种界限。