Wagner B, Radbruch A, Richards C, Leibold W
Immunology Unit, Hannover School of Veterinary Medicine, Germany.
Vet Immunol Immunopathol. 1995 Jul;47(1-2):1-12. doi: 10.1016/0165-2427(94)05381-2.
In order to define equine immunoglobulins (Igs) and to produce monoclonal reference Igs we fused equine peripheral blood mononuclear cells with X63-Ag8.653 non Ig producing murine myeloma cells. A total of 29 equine Ig producing equi-murine heterohybridomas were obtained, of which ten expressed equine Ig for more than 3 months. One of these heterohybridoma lines produced monoclonal IgM, an equine isotype which has not been available in monoclonal form before. Four lines secreted equine IgG of two distinct Ig heavy chain types as assessed by the molecular weight (MW), while the remaining five lines expressed only equine Ig light chains. A sixth Ig light chain expressing variant was obtained by cloning of one of the IgG producing heterohybridoma lines. These monoclonal IgGs were compared with previously described equine IgG monoclonal antibodies (mabs) by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE). According to their MW we identified five groups of gamma-chains and four groups of Ig light chains.
为了定义马免疫球蛋白(Igs)并生产单克隆参考Igs,我们将马外周血单个核细胞与不产生Ig的X63-Ag8.653小鼠骨髓瘤细胞进行融合。共获得了29个产生马Ig的马-鼠异源杂交瘤,其中10个表达马Ig超过3个月。这些异源杂交瘤细胞系中的一个产生单克隆IgM,这是一种以前没有单克隆形式的马同种型。通过分子量(MW)评估,有4个细胞系分泌两种不同Ig重链类型的马IgG,而其余5个细胞系仅表达马Ig轻链。通过克隆其中一个产生IgG的异源杂交瘤细胞系获得了第六个表达Ig轻链的变体。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)将这些单克隆IgG与先前描述的马IgG单克隆抗体(mabs)进行比较。根据它们的MW,我们鉴定出五组γ链和四组Ig轻链。