Huang S W, Taylor G E
Clin Exp Immunol. 1982 May;48(2):375-80.
Normally, the injection of streptozotocin (STZ) at a lower dose (60 mg/kg body weight) to young (45 days old) CD-1 male mice produces a sustained hyperglycemia with the concomitant development of hypoinsulinemia and immune insulitis in the pancreas, both of which lead to insulin-dependent diabetes (IDD). In an effort to abort the development of IDD, pertussis vaccine (PV) was administered either intraperitoneally (n = 12) or intravenously (n = 12) 3 days prior to STZ injection. In contrast to the control group (n = 12) which received only STZ resulting in the subsequent development of IDD after 16 weeks, none of the vaccinated group developed IDD. The complete protective effect was evidenced by normal insulin values, normoglycemia, the lack of the development of nucleic acid antibody and the absence of insulitis in the vaccinated animals. Under these experimental conditions, PV appeared to offer satisfactory protection of the beta cells of islets in pancreas against the inflammatory effect of STZ.
通常情况下,给年轻的(45日龄)CD - 1雄性小鼠注射低剂量(60毫克/千克体重)的链脲佐菌素(STZ)会导致持续的高血糖,并伴随胰腺中胰岛素分泌不足和免疫性胰岛炎的发展,这两者都会导致胰岛素依赖型糖尿病(IDD)。为了阻止IDD的发展,在注射STZ前3天,通过腹腔注射(n = 12)或静脉注射(n = 12)给予百日咳疫苗(PV)。与仅接受STZ注射并在16周后发展为IDD的对照组(n = 12)相比,接种疫苗的组中没有一只小鼠发展为IDD。接种疫苗的动物胰岛素值正常、血糖正常、未产生核酸抗体且没有胰岛炎,这些都证明了完全的保护作用。在这些实验条件下,PV似乎能对胰腺胰岛β细胞提供令人满意的保护,使其免受STZ的炎症影响。