Saha A R, Ueno K, Ohmori S, Igarashi T, Kitagawa H
Laboratory of Biochemical Pharmacology and Biotoxicology, Faculty of Pharmaceutical Sciences, Chiba University, Japan.
Jpn J Pharmacol. 1988 Dec;48(4):417-22. doi: 10.1254/jjp.48.417.
Heptaminol AMP amidate (HAA), a newly developed nucleotide derivative, was found to restore the immunosuppression in mice due to the induction of suppressor T (Ts) cells by concanavalin A (Con A) (50 micrograms/body). HAA also inhibited Con A-mediated in vitro induction of Ts cells. On the contrary, the administration of HAA in mice primed with keyhole lympet hemocyanin (KLH) (30 micrograms/body) caused an enhanced induction of antigen specific helper T (Th) cells. Effects of HAA on Ts and Th cells were found to be dependent on their level of induction. The administration of HAA also increased the spleen cell number and augmented the plaque forming cell response to some extent in cyclophosphamide treated mice. The present results suggested that HAA-mediated immunopotentiation was possible by a combined suppressive effect on Ts cells and enhancing effect on Th cells.
庚胺醇 AMP 酰胺化物(HAA)是一种新开发的核苷酸衍生物,发现它可恢复小鼠因伴刀豆球蛋白 A(Con A)(50 微克/只)诱导抑制性 T(Ts)细胞而导致的免疫抑制。HAA 还抑制 Con A 介导的 Ts 细胞体外诱导。相反,给预先用钥孔戚血蓝蛋白(KLH)(30 微克/只)致敏的小鼠施用 HAA,会增强抗原特异性辅助性 T(Th)细胞的诱导。发现 HAA 对 Ts 和 Th 细胞的作用取决于它们的诱导水平。在环磷酰胺处理的小鼠中,施用 HAA 还增加了脾细胞数量,并在一定程度上增强了空斑形成细胞反应。目前的结果表明,HAA 介导的免疫增强作用可能是通过对 Ts 细胞的联合抑制作用和对 Th 细胞的增强作用实现的。