Primi D, Mami F, Le Guern C, Cazenave P A
J Exp Med. 1982 Sep 1;156(3):924-9. doi: 10.1084/jem.156.3.924.
On the basis of previous frequency determinations we could set up large numbers of cultures, each containing less than one competent precursor B cell specific for beta-galactosidase or for each of three idiotopes previously found on a monoclonal anti-beta-galactosidase antibody. Cultures were polyclonally activated by either lipopolysaccharide or Nocardia-delipidated cell mitogen. Each culture supernatant was individually tested for hemagglutination activity against sheep erythrocytes coupled with beta-galactosidase or with each of the three purified monoclonal anti-idiotypic antibodies. The results showed that only a minority of those clones positive for only one or two idiotopes recognized antigen. However, all those clones simultaneously positive for the three V region determinants recognized beta-galactosidase. The implications of these results for our understanding of the relationship between the antigen-binding site and idiotope expression are discussed.
根据先前的频率测定结果,我们能够建立大量培养物,每个培养物中含有少于一个对β-半乳糖苷酶或先前在单克隆抗β-半乳糖苷酶抗体上发现的三种独特型之一具有反应能力的前体B细胞。培养物通过脂多糖或经脱脂的诺卡氏菌细胞促细胞分裂剂进行多克隆激活。对每个培养物的上清液分别进行检测,以测定其针对与β-半乳糖苷酶或三种纯化的单克隆抗独特型抗体之一偶联的绵羊红细胞的血凝活性。结果显示,仅对一种或两种独特型呈阳性的那些克隆中,只有少数能识别抗原。然而,所有同时对三个V区决定簇呈阳性的那些克隆都能识别β-半乳糖苷酶。讨论了这些结果对于我们理解抗原结合位点与独特型表达之间关系的意义。