Victor-Kobrin C, Bona C, Pernis B
Mount Sinai School of Medicine, New York, New York.
J Mol Cell Immunol. 1984;1(6):331-46.
The membrane expression of the J558 idiotype on B and T lymphocytes was studied in (A/J x BALB/c)F1 and (CAL.20 x BALB/c)F1 mice who were maternally suppressed for this idiotype. Animals suppressed in this fashion exhibit a chronic inability to synthesize J558 Id bearing antibodies in response to an antigenic challenge by alpha 1,3 linked dextran. However, by immunofluorescence, we observed that these maternally suppressed animals actually exhibited a considerable increase of B lymphocytes, which bear endogenously synthesized membrane immunoglobulin expressing the J558-IdI. Furthermore, a subset of T cells emerges that we have previously described as Lyt2.2+ cells exhibiting the J558-IdI determinant, which are capable of transferring the suppression to naïve recipients [1]. The goal of the experiments described in this communication was to thoroughly characterize those B cell clones that are expanded during idiotype suppression. Therefore, we immortalized these J558 Id+ B cells from idiotype suppressed mice as hybridomas. Four hybridomas secreting monoclonal antibodies bearing the J558 IdI but devoid of any specificity for alpha 1,3 linked dextran were obtained. It was established that these monoclonal antibodies bear the J558-Id by two criteria; namely, their direct binding to a panel of monoclonal anti-J558 IdI and a single anti-J558 IdX antibody, as well as by blocking the interaction of J558 with these antibodies. Notable was the fact that they all bore kappa light chains, even though in anti-dextran antibodies the expression of the lambda light chain is required for the expression of this idiotype. These results reaffirm the notion that idiotypic determinants are three dimensional structures which can be reconstructed by a variety of heavy and light chain sequences. Furthermore, an idiotope used in the regulation of an immune response (as our data implicate the J558 IdI is) is borne by antibodies displaying diverse specificities, which are coordinately regulated through this common idiotope.
在母源抑制该独特型的(A/J×BALB/c)F1和(CAL.20×BALB/c)F1小鼠中,研究了B和T淋巴细胞上J558独特型的膜表达。以这种方式被抑制的动物表现出长期无法在受到α1,3连接的葡聚糖抗原攻击时合成带有J558 Id的抗体。然而,通过免疫荧光,我们观察到这些母源抑制的动物实际上表现出表达内源性合成的膜免疫球蛋白且带有J558-IdI的B淋巴细胞显著增加。此外,出现了一个T细胞亚群,我们之前将其描述为表现出J558-IdI决定簇的Lyt2.2+细胞,它们能够将抑制作用传递给未接触过抗原的受体[1]。本通讯中描述的实验目的是全面表征在独特型抑制期间扩增的那些B细胞克隆。因此,我们将来自独特型抑制小鼠的这些J558 Id+ B细胞永生化成为杂交瘤。获得了四种分泌带有J558 IdI但对α1,3连接的葡聚糖无任何特异性的单克隆抗体的杂交瘤。通过两个标准确定这些单克隆抗体带有J558-Id;即,它们与一组单克隆抗J558 IdI和一种单克隆抗J558 IdX抗体的直接结合,以及通过阻断J558与这些抗体的相互作用。值得注意的是,它们都带有κ轻链,尽管在抗葡聚糖抗体中,该独特型的表达需要λ轻链的表达。这些结果再次证实了独特型决定簇是三维结构,其可由多种重链和轻链序列重建的观点。此外,如我们的数据所暗示的,用于调节免疫反应的一个独特位(J558 IdI)由具有不同特异性的抗体携带,这些抗体通过这个共同的独特位受到协同调节。