Brunswick M, Finkelman F D, Highet P F, Inman J K, Dintzis H M, Mond J J
Department of Medicine, Uniformed Services University, Bethesda, MD 20814.
J Immunol. 1988 May 15;140(10):3364-72.
To investigate the properties which enable type 2 Ag, as exemplified by dextran and Ficoll, to stimulate high levels of antibody responses in the relative absence of T cells, we conjugated anti-IgD and anti-IgM mAb to both dextran and Ficoll and examined their B cell-activating properties. Such conjugated anti-Ig antibodies stimulated both early and later stages of B cell activation at picogram concentrations, which are at least 1000-fold lower than that required for B cell stimulation by unconjugated anti-Ig antibodies, and the level of proliferation they stimulated was on average 10-fold greater. Furthermore, concentrations of anti-Ig dextran (100 pg/ml) which modulated little sIgD from the B cell surface were strong inducers of enhanced B cell expression of MHC class II molecules. Conjugation of Fab fragments of anti-IgD or nonmitogenic anti-IgM mAb to dextran rendered them as mitogenic as dextran conjugated to strongly stimulatory anti-IgD or anti-IgM antibodies. The ability of dextran and Ficoll to serve as effective carrier molecules for anti-IgD was not related solely to their large m.w., because anti-IgD coupled to polymerized BSA (m.w. 1.5 X 10(6), was only 10- to 50-fold more potent than unconjugated anti-IgD antibodies at stimulating B cell DNA synthesis. These results suggest, therefore, that the unique ability of picogram concentrations of haptenated type 2 Ag to stimulate Ig secretion in the absence of T cells may be a function of their ability to promote effective cross-linking without resulting in the modulation of sIg. This would enable such Ag to mediate repetitive B cell signaling, a situation that cannot be achieved by unconjugated anti-Ig antibodies which result in modulation of sIg at their mitogenic concentrations. These compounds therefore may be employed to study B cell activation stimulated by sIg cross-linking at concentrations that may more closely reflect those which are achieved under physiologic conditions by type 2 Ag.
为了研究诸如右旋糖酐和聚蔗糖等2型抗原在相对缺乏T细胞的情况下能够刺激高水平抗体反应的特性,我们将抗IgD和抗IgM单克隆抗体与右旋糖酐和聚蔗糖进行偶联,并检测它们的B细胞激活特性。这种偶联的抗Ig抗体在皮克浓度下就能刺激B细胞激活的早期和后期阶段,这比未偶联的抗Ig抗体刺激B细胞所需的浓度至少低1000倍,而且它们刺激的增殖水平平均高10倍。此外,抗Ig右旋糖酐浓度为100 pg/ml时,对B细胞表面sIgD的调节作用很小,但却是增强B细胞MHC II类分子表达的强诱导剂。将抗IgD的Fab片段或无丝裂原性的抗IgM单克隆抗体与右旋糖酐偶联后,它们就具有了与偶联强刺激性抗IgD或抗IgM抗体的右旋糖酐一样的丝裂原性。右旋糖酐和聚蔗糖作为抗IgD有效载体分子的能力并不完全与其高分子量有关,因为偶联到聚合牛血清白蛋白(分子量1.5×10⁶)上的抗IgD在刺激B细胞DNA合成时,其效力仅比未偶联的抗IgD抗体强10至50倍。因此,这些结果表明,皮克浓度的半抗原化2型抗原在无T细胞时刺激Ig分泌的独特能力可能是其促进有效交联而不导致sIg调节的能力的一种体现。这将使此类抗原能够介导重复性的B细胞信号传导,而未偶联的抗Ig抗体在其丝裂原浓度下会导致sIg调节,无法实现这种情况。因此,这些化合物可用于研究在更接近2型抗原在生理条件下所达到的浓度下,由sIg交联刺激的B细胞激活。