Suleyman S, Hosono O, Sioud M, Randen I, Thompson K M, Førre O, Natvig J B
Institute of Immunology and Rheumatology, Rikshospitalet, University of Oslo, Norway.
J Immunol. 1993 Jun 15;150(12):5466-75.
This article describes the characterization of a mouse monoclonal anti-idiotypic antibody (1H7B) prepared against a human monoclonal rheumatoid factor (RFSJ2) whose L chain utilized a V lambda I subgroup gene. The mAb 1H7B reacted with 6 of the tested 12 human V lambda I proteins, as well as with a newly produced lambda mAb whose V lambda gene usage has not as yet been determined. Because six of the 1H7B-positive mAb were heterogeneous with respect to both their VH gene utilization and antigenic specificity, and because mAb 1H7B did not react with any of the tested 43 kappa or 12 lambda proteins belonging to various subgroups other than V lambda I, mAb 1H7B appeared to be a V lambda I subgroup-specific reagent. The L chain specificity of mAb 1H7B was confirmed by Western blotting, and the inhibition of RFSJ2 binding to human Fc gamma by 1H7B provided additional evidence for the V region specificity of mAb 1H7B. The 11 sequenced V lambda I proteins used in this study were assigned to sub-subgroups by comparison with the previously published germ-line V lambda Ia, V lambda Ib, and V lambda Ic sequences. The mAb 1H7B only appeared to recognize V lambda Ia proteins as it reacted with five of the seven V lambda Ia, but not with three V lambda Ib or with one V lambda Ic protein. Because mAb 1H7B reacted with at least one V lambda Ia sequence in germ-line configuration, it appeared to be a marker for V lambda Ia sub-subgroup germ-line gene(s). The idiotope recognized by 1H7B was localized to the first framework region by inhibiting its binding to RFSJ2 with a synthetic peptide to the 11-24 amino acid region of V lambda Ia L chains. Comparison of the V lambda 1-24 region sequence of RFSJ2 with those of the two 1H7B-negative V lambda Ia mAb revealed a single amino acid difference at position 17, suggesting that the idiotope recognized by 1H7B encompassed this position.
本文描述了一种小鼠单克隆抗独特型抗体(1H7B)的特性,该抗体是针对一种人单克隆类风湿因子(RFSJ2)制备的,其轻链利用了VλI亚群基因。单克隆抗体1H7B与12种测试的人VλI蛋白中的6种发生反应,还与一种新产生的λ单克隆抗体发生反应,其Vλ基因的使用情况尚未确定。由于1H7B阳性单克隆抗体中的6种在VH基因利用和抗原特异性方面均具有异质性,且1H7B单克隆抗体不与属于VλI以外各种亚群的43种κ蛋白或12种λ蛋白中的任何一种发生反应,因此1H7B单克隆抗体似乎是一种VλI亚群特异性试剂。通过蛋白质印迹法证实了1H7B单克隆抗体的轻链特异性,并且1H7B对RFSJ2与人Fcγ结合的抑制作用为1H7B单克隆抗体的V区特异性提供了额外证据。通过与先前发表的种系VλIa、VλIb和VλIc序列进行比较,将本研究中使用的11种测序VλI蛋白分配到亚亚群。1H7B单克隆抗体似乎只识别VλIa蛋白,因为它与7种VλIa中的5种发生反应,但不与3种VλIb或1种VλIc蛋白发生反应。由于1H7B单克隆抗体与种系构型中的至少一种VλIa序列发生反应,它似乎是VλIa亚亚群种系基因的一个标记。通过用针对VλIa轻链11 - 24氨基酸区域的合成肽抑制其与RFSJ2的结合,将1H7B识别的独特型表位定位到第一个构架区。将RFSJ2的Vλ1 - 24区域序列与两种1H7B阴性VλIa单克隆抗体的序列进行比较,发现在第17位有一个氨基酸差异,这表明1H7B识别的独特型表位包含该位置。