Nisonoff A, Ju S T
Fed Proc. 1977 Feb;36(2):207-13.
Antibodies elicited in strain A mice by immunization with keyhole limpet hemocyanin-p-azophenylarsonate (KLH-Ar) produce anti-Ar antibodies, some of which share a cross-reactive idiotype (CRI); in general, 20 to 70% of the antihapten antibody population carries the idiotype. Large amounts of antibody can be produced by the induction of ascitic fluids, using a 9:1 ratio of complete Freund's adjuvant (CFA) to antigen. Antibodies with the CRI can be isolated by isoelectric focusing from selected mice that have produced a high concentration of the CRI. The H chains exhibit a single homogeneous sequence through the first hypervariable region and, when isolated from a large number of individual mice, appear to be invariant in the first framework region. These findings indicate that somatic mutation is not a significant factor in the determination of framework sequences. Appearance of the CRI can be suppressed in adult A/J mice by administration of rabbit anti-idiotypic antiserum prior to immunization. Such suppressed mice produce normal concentrations of anti-Ar antibodies lacking the CRI. Anti-idiotypic antibodies produced against such antibodies failed to show cross-reactivity with anti-Ar antibodies arising in idiotypically suppressed or nonsuppressed A/J mice. The great sensitivity of the assay indicates that the number of such "private" idiotypes, all present on anti-Ar antibodies of a single strain, must be extremely large; this supports a somatic mechanism for the generation of diversity. The "private" idiotypes arising in suppressed, hyperimmunized mice can be adoptively transferred into multiple, irradiated (200 R) recipients by injections of spleen cells or of cells from ascitic fluids. The use of ascitic fluids permits the rapid production of a colony of mice bearing the idiotype. This should facilitate structural studies of a variety of idiotypically different molecules sharing the same (anti-Ar) specificity, as well as studies of the mechanism of suppression.
用钥孔戚血蓝蛋白 - 对氨基苯胂酸(KLH - Ar)免疫A品系小鼠所产生的抗体能产生抗胂酸抗体,其中一些抗体具有交叉反应独特型(CRI);一般来说,20%至70%的抗半抗原抗体群体带有这种独特型。使用完全弗氏佐剂(CFA)与抗原9:1的比例诱导腹水可产生大量抗体。具有CRI的抗体可通过等电聚焦从产生高浓度CRI的选定小鼠中分离出来。重链在第一个高变区呈现单一的同源序列,并且当从大量个体小鼠中分离时,在第一个构架区似乎是不变的。这些发现表明体细胞突变不是决定构架序列的重要因素。在成年A/J小鼠免疫前给予兔抗独特型抗血清可抑制CRI的出现。这种受抑制的小鼠产生正常浓度的缺乏CRI的抗胂酸抗体。针对此类抗体产生的抗独特型抗体与在独特型受抑制或未受抑制的A/J小鼠中产生的抗胂酸抗体未显示交叉反应。该检测方法的高灵敏度表明,所有存在于单一品系抗胂酸抗体上的此类“私有”独特型的数量必定极其庞大;这支持了多样性产生的体细胞机制。在受抑制的超免疫小鼠中产生的“私有”独特型可通过注射脾细胞或腹水细胞将其过继转移到多个经照射(200伦琴)的受体小鼠中。使用腹水可快速产生带有该独特型的小鼠群体。这应有助于对具有相同(抗胂酸)特异性的各种独特型不同分子进行结构研究,以及对抑制机制的研究。