Van Snick J L, Stassin V, de Lestré B
J Exp Med. 1983 Mar 1;157(3):1006-19. doi: 10.1084/jem.157.3.1006.
The specificity of polyclonal mouse rheumatoid factors (RF) was analyzed by competition experiments with heat-aggregated mouse IgG subclasses. The RF spontaneously produced by three normal mouse strains (129/Sv, CBA/Ht, and C57Bl/6) and by two strains with autoimmune diseases (MRL/l and NZB) were found to consist of distinct non-cross-reactive antibody subpopulations each specific for one IgG subclass. The sera of the normal strains contained IgG1- and IgG2a-specific RF. The autoimmune strains produced an additional variety of RF that was specific for The autoimmune strains produced an additional variety of RF that was specific for IgG2b. Also, the RF secreted by spleen cells of various normal strains after in vitro polyclonal activation with lipopolysaccharide could be resolved into distinct subpopulations specific for IgG1 or IgG2a. These results were confirmed by the analysis of monoclonal RF derived from BALB/c, C57Bl/6, CBA/Ht, and 129/Sv mice: of 73 hybridomas with RF activity, 71 displayed a strict subclass specificity. The subclass predominantly recognized depended on the origin of the spleen cells used to generate the hybridomas. After polyclonal activation in vitro, a broad spectrum of different specificities was obtained with 16 RF specific for IgG1, 13 for IgG2a, and 4 for IgG2b. In contrast, 27 of 28 monoclonal RF derived from 129/Sv and BALB/c mice without prior polyclonal activation were specific for IgG2a, and of these 75% were allotype specific since they failed to react with IgG2a of the b allotype. These results demonstrate the importance of subclass specificity in the production of RF in vivo. With the exception of the IgG2b-specific clones, all these monoclonal RF reacted preferentially with heat-aggregated or antigen-bound IgG. Among the hybridomas generated by the fusion of in vitro polyclonally activated spleen cells of 4-wk-old mice, the frequency of clones with RF activity was at least 40 times higher than that of clones specific for mouse IgM, human IgG, ovalbumin, and hen lysozyme.
通过与热聚集的小鼠IgG亚类进行竞争实验,分析了多克隆小鼠类风湿因子(RF)的特异性。发现三种正常小鼠品系(129/Sv、CBA/Ht和C57Bl/6)以及两种患有自身免疫性疾病的品系(MRL/l和NZB)自发产生的RF由不同的非交叉反应性抗体亚群组成,每个亚群对一种IgG亚类具有特异性。正常品系的血清含有针对IgG1和IgG2a的RF。自身免疫品系产生了另外多种针对IgG2b的RF。此外,用脂多糖进行体外多克隆激活后,各种正常品系脾细胞分泌的RF可分解为针对IgG1或IgG2a的不同亚群。对源自BALB/c、C57Bl/6、CBA/Ht和129/Sv小鼠的单克隆RF的分析证实了这些结果:在73个具有RF活性的杂交瘤中,71个表现出严格的亚类特异性。主要识别的亚类取决于用于产生杂交瘤的脾细胞的来源。体外多克隆激活后,获得了广泛的不同特异性,其中16种RF针对IgG1,13种针对IgG2a,4种针对IgG2b。相比之下,来自未经预先多克隆激活的129/Sv和BALB/c小鼠的28个单克隆RF中有27个对IgG2a具有特异性,其中75%是同种异型特异性的,因为它们不能与b同种异型的IgG2a反应。这些结果证明了亚类特异性在体内RF产生中的重要性。除了针对IgG2b的克隆外,所有这些单克隆RF都优先与热聚集的或抗原结合的IgG反应。在由4周龄小鼠体外多克隆激活的脾细胞融合产生的杂交瘤中,具有RF活性的克隆频率比针对小鼠IgM、人IgG、卵清蛋白和鸡溶菌酶的克隆频率至少高40倍。