Ben-Anat Porat Y, Zan-Bar I
Department of Human Microbiology, Sackler School of Medicine, Tel-Aviv University, Israel.
Clin Immunol Immunopathol. 1995 Feb;74(2):151-5. doi: 10.1006/clin.1995.1022.
Human-human B cell hybridoma JK32.1, constructed from B lymphocytes of a common variable immunodeficient patient and nonsecreting cell line, retains the defects of B cell immunodeficiency. Efforts to clarify whether the defect is located within the plasma membranes of this cell line were carried out by implanting them with plasma membrane fraction derived from normal functional cells via intact non-infectious Sendai virus. The implanted cells were activated with various mitogens and their Ig responses and isotype switching were examined. Restoration of IgM secretion was achieved in the implanted JK32.1 cells following stimulation with SAC, PWM, or retinoic acid. Augmented IgM response was also obtained in the implanted cells treated with retinoic acid and lipopolysaccharide (LPS) despite their unresponsiveness to LPS alone. No IgG or IgA response could be detected in the implanted JK32.1 cells. These data suggest that this immunodeficient cell line possesses at least two different malfunctions, one located within the plasma membrane moiety of the cells and the other located within the cytoplasmic and/or nucleic components. The plasma membrane moiety defect can be repaired temporarily by delivering proper signals via the implanted plasma membranes. However, this manipulation of the cells could not overcome the intrinsic defect of the cells which blocks isotype switching and secretion of IgG, IgE, and IgA antibodies.
人-人B细胞杂交瘤JK32.1由一名常见可变免疫缺陷患者的B淋巴细胞与非分泌细胞系构建而成,保留了B细胞免疫缺陷的特征。通过用源自正常功能细胞的质膜组分经完整的非感染性仙台病毒植入该细胞系,来努力阐明该缺陷是否位于其质膜内。用各种有丝分裂原激活植入的细胞,并检测它们的Ig反应和同种型转换。在用SAC、PWM或视黄酸刺激后,植入的JK32.1细胞实现了IgM分泌的恢复。在用视黄酸和脂多糖(LPS)处理的植入细胞中,尽管它们对单独的LPS无反应,但也获得了增强的IgM反应。在植入的JK32.1细胞中未检测到IgG或IgA反应。这些数据表明,这种免疫缺陷细胞系至少存在两种不同的功能障碍,一种位于细胞的质膜部分,另一种位于细胞质和/或核酸成分中。通过植入的质膜传递适当的信号,可以暂时修复质膜部分的缺陷。然而,这种对细胞的操作无法克服细胞内在的缺陷,该缺陷阻碍了IgG、IgE和IgA抗体的同种型转换和分泌。