Lydyard P M, MacKenzie L E, Youinou P Y, Deane M, Jefferis R, Mageed R A
Department of Immunology, University College and Middlesex School of Medicine, London, United Kingdom.
Ann N Y Acad Sci. 1992 May 4;651:527-39. doi: 10.1111/j.1749-6632.1992.tb24659.x.
Epstein-Barr virus (EBV)-immortalized monoclonal B-cell lines were established from CD5+ and CD5- cord-blood B cells. IgM from many of both CD5+ and CD5- clones reacted with IgG-Fc, ssDNA, and a variety of other autoantigens. More CD5+ B cells that used light chains of the kappa isotype reacted with IgG-Fc and ssDNA than kappa-bearing CD5- B cells. Because many of the clones reacted with IgG-Fc, they were analyzed for the expression of cross-reactive idiotypes (CRI) associated with rheumatoid factor and cold agglutinin paraproteins using murine antibodies (mAb) recognizing V kappa and VH subgroup-associated determinants. Expression of the V kappa IIIb sub-subgroup-associated idiotope recognized by 17.109 mAb was expressed at significantly higher frequency (32%; p less than 0.05) and IgM antibodies derived from the CD5+ compared with the CD5- clones (5%). Both CD5+ and CD5- clones expressed the RF paraprotein-associated idiotope recognized by G8 mAb to the same extent. Similar results were obtained using binding to SpA as a marker of VH III family usage. Furthermore, no differences in frequency of expression of RF paraprotein-associated idiotopes recognized by B6 and/or D12, and characteristic of some antibodies using VH III family genes, were found between the CD5+ and CD5- populations. Although a higher than expected frequency of VH IV-gene expression was demonstrated (around 30%) in both CD5+ and CD5- cells, there were differences in expression of CRI recognized by mAb Lc1 and R2.1A2 with specificities for two VH IV subfamilies. While some CD5+ and CD5- clones were identified in which their IgM reacted with mAb Lc1, only CD5+ clones were recognized by another mAb R2.1A2. Analysis of the relationships between antigen specificities and V kappa- and VH-family gene usage indicated that auto- or polyreactivity was not associated with V kappa III nor any particular VH family. The higher frequency of the V kappa IIIb sub-subgroup-associated idiotope recognized by 17-109 in the CD5+ clones and the association of CD5+ B cells with the VH IV subfamily recognized by mAb R2.1A2 and 9G4 may suggest that CD5+ B cells in cord blood are expanded as a result of recruitment within the fetal environment.
从CD5 +和CD5 -脐血B细胞建立了爱泼斯坦-巴尔病毒(EBV)永生化的单克隆B细胞系。许多CD5 +和CD5 -克隆的IgM与IgG-Fc、单链DNA以及多种其他自身抗原发生反应。与携带κ链的CD5 - B细胞相比,更多使用κ同种型轻链的CD5 + B细胞与IgG-Fc和单链DNA发生反应。由于许多克隆与IgG-Fc发生反应,因此使用识别Vκ和VH亚组相关决定簇的鼠源抗体(mAb)分析了与类风湿因子和冷凝集素副蛋白相关的交叉反应性独特型(CRI)的表达。由17.109 mAb识别的VκIIIb亚亚组相关独特型的表达在CD5 +克隆中频率显著更高(32%;p小于0.05),而与CD5 -克隆(5%)相比。CD5 +和CD5 -克隆在相同程度上表达了由G8 mAb识别的RF副蛋白相关独特型。以与葡萄球菌A蛋白(SpA)结合作为VH III家族使用的标志物也获得了类似结果。此外,在CD5 +和CD5 -群体之间,未发现由B6和/或D12识别的RF副蛋白相关独特型的表达频率以及使用VH III家族基因的某些抗体的特征存在差异。尽管在CD5 +和CD5 -细胞中均显示出VH IV基因表达频率高于预期(约30%),但对于两个VH IV亚家族具有特异性的mAb Lc1和R2.1A2识别的CRI表达存在差异。虽然鉴定出一些CD5 +和CD5 -克隆,其IgM与mAb Lc1发生反应,但只有CD5 +克隆被另一种mAb R2.1A2识别。对抗原特异性与Vκ和VH家族基因使用之间关系的分析表明,自身反应性或多反应性与VκIII或任何特定的VH家族均无关。17 - 109在CD5 +克隆中识别的VκIIIb亚亚组相关独特型的较高频率以及CD5 + B细胞与由mAb R2.1A2和9G4识别的VH IV亚家族的关联可能表明,脐血中的CD5 + B细胞是由于在胎儿环境中的募集而扩增的。