Chen P, Farrar J J, Oppenheim J J, Mergenhagen S E
Infect Immun. 1977 Sep;17(3):567-71. doi: 10.1128/iai.17.3.567-571.1977.
The immunoenhancing activity of a water-soluble extract of dental plaque (DP), which contains a mixture of microbial antigens, has been investigated. DP was tested for its capacity to augment the in vitro antibody-forming cell (AFC) response to sheep erythrocyte by adherent spleen cells from thymectomized, lethally irradiated, and bone marrow-transplanted (TxB) mice. Although DP was found to induce a small polyclonal AFC response, most of the increase in AFC induced by DP was antigen dependent. The latter enhancing effect is an indicator of the adjuvanticity of DP. This adjuvant activity of DP was T-cell-dependent, since removal of the residual prethymic and/or thymic-derived lymphocytes (T-cells) by anti-T-cell serum (anti-theta) and guinea pig complement abrogated the capacity of DP to augment the in vitro AFC response. This view was further supported by the synergistic restorative effect obtained by culturing anti-theta-treated adherent spleen cells with both DP and a population of unactivated T-cells that by themselves were unable to significantly enhance AFC responsiveness. Moreover, DP was found to be mitogenic for thymocytes. The cumulative results suggest that the adjuvant activity of DP is dependent on both the T- and B-cell-activating components present in DP.
已对含有多种微生物抗原混合物的牙菌斑(DP)水溶性提取物的免疫增强活性进行了研究。通过来自胸腺切除、致死性照射和骨髓移植(TxB)小鼠的贴壁脾细胞,检测了DP增强对绵羊红细胞体外抗体形成细胞(AFC)反应的能力。虽然发现DP可诱导小的多克隆AFC反应,但DP诱导的AFC增加大多是抗原依赖性的。后一种增强作用是DP佐剂活性的指标。DP的这种佐剂活性是T细胞依赖性的,因为用抗T细胞血清(抗θ)和豚鼠补体去除残留的胸腺前和/或胸腺来源的淋巴细胞(T细胞)消除了DP增强体外AFC反应的能力。通过将抗θ处理的贴壁脾细胞与DP和一群本身不能显著增强AFC反应性的未活化T细胞一起培养获得的协同恢复效应进一步支持了这一观点。此外,发现DP对胸腺细胞有促有丝分裂作用。累积结果表明,DP的佐剂活性取决于DP中存在的T细胞和B细胞激活成分。