Stadtländer C T, Gangemi J D, Khanolkar S S, Kitsos C M, Farris H E, Fulton L K, Hill J E, Huntington F K, Lee C K, Monath T P
Greenville Hospital System/Clemson University Biomedical Cooperative, Department of Microbiology, South Carolina 29634, USA.
Dig Dis Sci. 1996 Sep;41(9):1853-62. doi: 10.1007/BF02088757.
Groups of squirrel monkeys (Saimiri spp.), predetermined to be free of Helicobacter infections in the gastric mucosa, were immunized orally with 0.5-4.5 mg of Helicobacter pylori recombinant urease (rUrease) and 25-500 micrograms of Escherichia coli heat-labile enterotoxin (LT) adjuvant. Oral immunization with rUrease resulted in a markedly elevated serum immunoglobulin G (IgG) antibody response with peak levels at 45 days after immunization. No significant gastric inflammation or cytotoxicity was evident in rUrease immunized monkeys as determined by light and electron microscopy. Twenty-five micrograms of LT was a sufficient and safe adjuvant dosage, whereas higher dosages resulted in diarrhea and lethargy. Animals developed a serum IgG antibody response to LT that did not impede the production of anti-rUrease antibody levels. The results of this investigation indicate that rUrease is immunogenic in a nonhuman primate.
预先确定胃黏膜无幽门螺杆菌感染的松鼠猴(僧面猴属)组,用0.5 - 4.5毫克幽门螺杆菌重组脲酶(rUrease)和25 - 500微克大肠杆菌不耐热肠毒素(LT)佐剂进行口服免疫。用rUrease口服免疫导致血清免疫球蛋白G(IgG)抗体反应显著升高,在免疫后45天达到峰值水平。通过光学和电子显微镜检查确定,接受rUrease免疫的猴子没有明显的胃部炎症或细胞毒性。25微克的LT是足够且安全的佐剂剂量,而更高剂量会导致腹泻和嗜睡。动物对LT产生血清IgG抗体反应,但这并不妨碍抗rUrease抗体水平的产生。这项研究结果表明,rUrease在非人类灵长类动物中具有免疫原性。