Steinitz M, Klein G
J Immunol. 1980 Jul;125(1):194-6.
Surface IgA-positive human lymphocytes were selected, separated, and immortalized with Epstein-Barr virus (EBV). Selection was carried out by rosetting the cells with ox erythrocytes, coated with rabbit anti-human IgA immunoglobulin, followed by separation on Ficoll-Isopaque. Stable monoclonal lines were established by cloning in agarose. This shows that EBV-transformation is not restricted to the IgM-positive B cell category but can be extended to minority classes of B lymphocytes. The method provides the means to establish other minority categories as continuous lines, depending on the efficiency of the preselection procedure.
挑选出表面免疫球蛋白A(IgA)呈阳性的人类淋巴细胞,用爱泼斯坦-巴尔病毒(EBV)进行分离并使其永生化。通过用包被有兔抗人IgA免疫球蛋白的牛红细胞使细胞形成花环来进行挑选,随后在菲可-泛影葡胺上进行分离。通过在琼脂糖中克隆建立稳定的单克隆系。这表明EBV转化并不局限于IgM呈阳性的B细胞类别,而是可以扩展到少数类别的B淋巴细胞。该方法提供了一种手段,可根据预选程序的效率将其他少数类别建立为连续细胞系。