Brandely M, Lagrange P, Hurtrel B, Motta I, Truffa-Bachi P
Cell Immunol. 1985 Jul;93(2):280-91. doi: 10.1016/0008-8749(85)90134-0.
The effect of Suramin on the cell-mediated delayed-type hypersensitivity (DTH) and the humoral immune responses elicited in mice by sheep erythrocytes was studied. The results show that administration of Suramin, at various times before or after antigenic sensitization, results in a profound inhibition of cell-mediated responses but has no adverse effect on antibody production. Suramin was particularly effective when given during the effector phase of DTH: mice which were treated with this drug, 4 days after immunization, at the time of skin testing, exhibit negative or low DTH responses compared to control mice. Evidence is presented that this short-term Suramin-induced suppressive effect on the expression of DTH is related to a defective recruitment, by sensitized T lymphocytes, of phagocytic cells at the site of the inflammatory reaction. In addition, when treatment with Suramin precedes by 8 days (Day -8) or by 1 hr sensitization with sheep erythrocytes for DTH, decreased DTH reactions over controls were observed. The inhibitory effect exerted by Suramin administered on Day -8 can be reversed by increasing the dose, from 10(6) to 10(8) sheep erythrocytes, of the sensitizing antigen. The possibility is discussed that, in this case, Suramin may interfere with the generation of DTH-mediating cells through a rapid degradation of antigen related to the Suramin-induced hyperplasia of the mononuclear phagocyte system. In contrast, DTH anergy in mice treated with Suramin 1 hr before sensitization is maintained regardless of the sensitizing antigen dose. Analysis of the sensitized lymphocyte population in these mice indicates that Suramin does not prevent the induction of DTH-mediating cells and suggests that the expression of these latter is inhibited by suppressive cells which are generated as a result of drug treatment.
研究了苏拉明对绵羊红细胞在小鼠体内引发的细胞介导的迟发型超敏反应(DTH)和体液免疫反应的影响。结果表明,在抗原致敏之前或之后的不同时间给予苏拉明,会导致细胞介导的反应受到显著抑制,但对抗体产生没有不良影响。当在DTH的效应阶段给予苏拉明时,其效果尤为显著:在免疫后4天、皮肤测试时用该药物治疗的小鼠,与对照小鼠相比,表现出阴性或低DTH反应。有证据表明,苏拉明对DTH表达的这种短期抑制作用与致敏T淋巴细胞在炎症反应部位募集吞噬细胞的缺陷有关。此外,当在DTH用绵羊红细胞致敏前8天(第-8天)或1小时给予苏拉明治疗时,观察到与对照相比DTH反应降低。在第-8天给予的苏拉明所施加的抑制作用可通过增加致敏抗原的剂量(从10⁶增加到10⁸个绵羊红细胞)来逆转。讨论了在这种情况下,苏拉明可能通过与苏拉明诱导的单核吞噬细胞系统增生相关的抗原快速降解来干扰DTH介导细胞的产生。相反,在致敏前1小时用苏拉明治疗的小鼠中的DTH无反应性不受致敏抗原剂量的影响而持续存在。对这些小鼠中致敏淋巴细胞群体的分析表明,苏拉明不会阻止DTH介导细胞的诱导,并表明这些细胞的表达受到药物治疗产生的抑制细胞的抑制。