Matthes T, Dighiero G
Département de Médecine, Institut Pasteur, Paris, France.
J Immunol. 1988 Jan 1;140(1):148-54.
Two monoclonal anti-idiotopic antibodies (anti-Id) were raised in mice against a human monoclonal IgA,K displaying a monospecific anti-tubulin (anti-alpha- and anti-beta-tubulin) activity. One anti-Id (IgG,K) recognized a private idiotope, TID 3.2, present only on the IgA,K immunogen, close to or within the antigen-combining site. The other anti-Id (IgM,K) recognized a recurrent idiotope, TID 7.1, outside the paratope and present in normal human and BALB/c mouse serum, on 2 of 11 polyspecific human monoclonal immunoglobulins and on 6 of 11 murine natural monoclonal auto-antibodies exhibiting a widespread anticytoskeletal protein-binding activity. Both the idiotopes were absent on two induced anti-tubulin antibodies exhibiting a monospecific anti-alpha- and anti-beta-tubulin specificity. Utilizing competitive and additivity immunoassays, we could show that the polyspecific human and mouse anticytoskeletal antibodies tested, whether bearing the TID 7.1 Id or not, appeared to compete in variable degrees for epitopes on the tubulin molecule recognized by the monoclonal IgA,K but distinct from the epitopes recognized by the induced monospecific anti-tubulin antibodies. The high incidence of the recurrent TID 7.1 idiotope in man and mouse suggests an important physiologic and perhaps regulatory function of this idiotope. Furthermore our data suggest that a restricted family of germ-line genes, highly conserved during phylogeny, may encode for these idiotope-bearing Ig molecules.
针对一种具有单特异性抗微管蛋白(抗α-和抗β-微管蛋白)活性的人单克隆IgAκ,在小鼠体内产生了两种单克隆抗独特型抗体(抗Id)。一种抗Id(IgGκ)识别一个仅存在于IgAκ免疫原上的独特型决定簇TID 3.2,它靠近抗原结合位点或在抗原结合位点内。另一种抗Id(IgMκ)识别一个重现性独特型决定簇TID 7.1,它位于互补位之外,存在于正常人血清和BALB/c小鼠血清中,在11种多特异性人单克隆免疫球蛋白中的2种以及11种具有广泛抗细胞骨架蛋白结合活性的小鼠天然单克隆自身抗体中的6种上也有发现。在两种诱导产生的具有单特异性抗α-和抗β-微管蛋白特异性的抗微管蛋白抗体上,这两种独特型决定簇均不存在。利用竞争性和加和性免疫测定,我们可以表明,所测试的多特异性人和小鼠抗细胞骨架抗体,无论是否带有TID 7.1独特型,似乎都在不同程度上竞争单克隆IgAκ所识别的微管蛋白分子上的表位,但与诱导产生的单特异性抗微管蛋白抗体所识别的表位不同。重现性TID 7.1独特型在人和小鼠中的高发生率表明该独特型具有重要的生理功能,也许还具有调节功能。此外,我们的数据表明,在系统发育过程中高度保守的一个有限的种系基因家族可能编码这些带有独特型的Ig分子。