Sverremark E, Fernandez C
Department of Immunology, The Wenner-Gren Institute, Arrhenius Laboratories for Natural Sciences, Stockholm University, Stockholm, Sweden.
Immunology. 1998 Nov;95(3):402-8. doi: 10.1046/j.1365-2567.1998.00612.x.
The bacterial carbohydrate dextran B512 is a thymus-independent (TI) antigen and a poor immunogen. Humoral responses consist primarily of IgM and no memory response is observed; rather, secondary responses to native dextran are similar to or suppressed compared with primary responses. However, immune responses to dextran can be enhanced. In this study we have used a protein-dextran conjugate that elicits a thymus-dependent (TD) immune response against dextran. Furthermore, we used the potent adjuvant cholera toxin (CT) for the dextran immunizations. This enables us to re-evaluate the phenomenon of poor secondary response to dextran and whether it can be abrogated. We show that native dextran-primed mice were not able to mount IgG anti-dextran antibody responses after repeated immunizations with the TD, protein-dextran conjugate. This was also apparent in the spleen, where almost no dextran-specific germinal centres were detected. However, the anti-protein antibody response was normal in these mice, demonstrating that it is only the anti-dextran-responding cells that are affected. The effect of CT adjuvant on these events was also evaluated. CT enhanced the humoral IgM anti-dextran responses as well as the splenic responses to dextran. But, the isotype profile was not altered, still no IgG was produced. In contrast, mice primed with the TD conjugate and repeatedly re-immunized with native, TI, dextran generated IgG anti-dextran responses. Our results indicate that it is probable that the lack of proper costimulation in the initiation of the response to dextran causes the suppressed secondary dextran responses. Furthermore, these results suggest that TI and TD forms of dextran activate the same type of B cells, since TI dextran-priming abrogated TD dextran IgG responses. The importance of the priming event for the induction of a classical memory response to carbohydrate antigens and the implications for vaccination strategies, are discussed.
细菌碳水化合物葡聚糖B512是一种非胸腺依赖性(TI)抗原,也是一种弱免疫原。体液反应主要由IgM组成,未观察到记忆反应;相反,与初次反应相比,对天然葡聚糖的二次反应相似或受到抑制。然而,对葡聚糖的免疫反应可以增强。在本研究中,我们使用了一种蛋白-葡聚糖偶联物,它能引发针对葡聚糖的胸腺依赖性(TD)免疫反应。此外,我们将强效佐剂霍乱毒素(CT)用于葡聚糖免疫。这使我们能够重新评估对葡聚糖二次反应不佳的现象以及这种现象是否可以消除。我们发现,用TD蛋白-葡聚糖偶联物反复免疫后,用天然葡聚糖预致敏的小鼠无法产生IgG抗葡聚糖抗体反应。这在脾脏中也很明显,几乎未检测到葡聚糖特异性生发中心。然而,这些小鼠中的抗蛋白抗体反应正常,表明只有抗葡聚糖反应细胞受到影响。还评估了CT佐剂对这些事件的影响。CT增强了体液IgM抗葡聚糖反应以及脾脏对葡聚糖的反应。但是,同种型谱未改变,仍然没有产生IgG。相比之下,用TD偶联物预致敏并反复用天然TI葡聚糖重新免疫的小鼠产生了IgG抗葡聚糖反应。我们的结果表明,对葡聚糖反应起始时缺乏适当的共刺激可能导致二次葡聚糖反应受到抑制。此外,这些结果表明,TI和TD形式的葡聚糖激活相同类型的B细胞,因为TI葡聚糖预致敏消除了TD葡聚糖IgG反应。讨论了致敏事件对诱导针对碳水化合物抗原的经典记忆反应的重要性以及对疫苗接种策略的影响。