Schuller G B, Morahan P S, Snodgrass M
Cancer Res. 1975 Aug;35(8):1915-20.
Inhibition or enhancement of Friend leukemia virus disease could be produced by treatment of mice with the immunopotentiator, pyran copolymer. The result depended on the route of inoculation of the drug. Prophylactic administration of the drug i.p. retarded splenomegaly, reduced splenic foci, and increased survival time of mice infected with Friend leukemia virus. Conversely, when the same dose and regimen of pyran was administered i.v., splenomegaly was enhanced, splenic foci were increased, and survival time was decreased. Histopathological examination of the spleens of mice revealed that i.p. pyran administration caused a marked increase in the splenic marginal zone with some increase in erythropoiesis in the red pulp, while i.v. pyran administration did not markedly change the splenic marginal zone but caused an early and sustained increase in erythropoiesis in the red pulp.
用免疫增强剂吡喃共聚物治疗小鼠,可抑制或增强弗瑞德白血病病毒病。结果取决于药物的接种途径。腹腔注射该药物进行预防性给药可延缓脾肿大,减少脾脏病灶,并延长感染弗瑞德白血病病毒小鼠的存活时间。相反,当通过静脉注射给予相同剂量和方案的吡喃时,脾肿大加剧,脾脏病灶增多,存活时间缩短。对小鼠脾脏进行组织病理学检查发现,腹腔注射吡喃会导致脾边缘区显著增加,红髓中的红细胞生成略有增加,而静脉注射吡喃并未明显改变脾边缘区,但会导致红髓中红细胞生成早期且持续增加。