Puttick A H, Williamson E A, Merry A H, Kumpel B M, Thompson K M, Jones V E
Postgraduate Medical School, University of Exeter, Devon, UK.
Ann Rheum Dis. 1988 Nov;47(11):898-905. doi: 10.1136/ard.47.11.898.
Human monoclonal anti-Rh(D) antibodies of known IgG isotype and Gm allotype were bound to erythrocytes and then used as the target IgG antigens for rheumatoid factors (RFs) in a direct haemagglutination test. When serum samples from patients with rheumatoid arthritis (RA) were tested for RF specificity towards these IgG monoclonal anti-D antibodies the incidence and titre of reactivity towards an IgG3 monoclonal anti-D antibody was considerably greater than for a polyclonal anti-D antibody of the same Gm allotype, G3m(5). This difference was not explained by the amount of each anti-D antibody which bound to erythrocytes. Furthermore, when patients with RA were divided into groups according to their Gm phenotype, sera from a greater proportion of patients negative for the phenotype G3m(5) reacted to the G3m(5) monoclonal anti-D antibodies than sera from those patients positive for this allotype. Analysis of RF reactivities towards two IgG3 and three IgG1 monoclonal anti-D antibodies, each with different Gm allotypic epitopes, indicated, however, that individual serum samples contained RFs with a spectrum of specificities; some sera appeared to react to a single set of Gm alleles, whereas others also reacted to isotypic or iso-allotypic epitopes, or both. Our data suggest that RFs with specificity for Gm allotypes do not arise in patients who carry that particular allotype owing to tolerance induced in fetal-neonatal life. Conversely, RFs with apparent specificity for a Gm allotype formed in patients negative for that allotype may be reacting to a closely related but different epitope. Final proof requires precise specificities for each RF formed, and IgG3 monoclonal anti-D antibodies would be useful reagents for this purpose.
已知IgG同种型和Gm异型的人源单克隆抗Rh(D)抗体与红细胞结合,然后在直接血凝试验中用作类风湿因子(RFs)的靶标IgG抗原。当检测类风湿关节炎(RA)患者血清样本对这些IgG单克隆抗-D抗体的RF特异性时,对IgG3单克隆抗-D抗体的反应发生率和滴度明显高于具有相同Gm异型G3m(5)的多克隆抗-D抗体。这种差异不能用与红细胞结合的每种抗-D抗体的量来解释。此外,当根据Gm表型将RA患者分组时,G3m(5)表型阴性的患者血清对G3m(5)单克隆抗-D抗体的反应比例高于该异型阳性患者的血清。然而,对两种IgG3和三种IgG1单克隆抗-D抗体(每种具有不同的Gm异型表位)的RF反应性分析表明,个体血清样本中含有具有一系列特异性的RFs;一些血清似乎只对一组Gm等位基因有反应,而另一些血清也对同种型或同种异型表位或两者都有反应。我们的数据表明,对Gm异型具有特异性的RFs不会在携带该特定异型的患者中产生,因为在胎儿-新生儿期诱导了耐受性。相反,在对该Gm异型呈阴性的患者中形成的对Gm异型具有明显特异性的RFs可能是对密切相关但不同的表位有反应。最终的证据需要确定每种形成的RF的精确特异性,而IgG3单克隆抗-D抗体将是用于此目的的有用试剂。