Robinson K, Bellaby T, Wakelin D
Department of Life Science, University of Nottingham, U.K.
Int J Parasitol. 1995 Aug;25(8):989-92. doi: 10.1016/0020-7519(94)00219-e.
Vaccination by different routes and with different adjuvants is known to influence profiles of immune responses and may be used to overcome genetically determined low-responsiveness to infection. A mouse model of infection with the intestinal nematode Trichinella spiralis was used to investigate the effect of mode of vaccination upon immune responsiveness and worm expulsion phenotype in high- (NIH) and low- (C57 BL/10) responder strains of mice. Muscle larval homogenate antigen was given subcutaneously in Freund's complete adjuvant (FCA) to induce a systemic immune response or with cholera toxin (CT) orally to stimulate mucosal immunity. Both approaches significantly protected NIH mice. Vaccination with FCA was correlated with elevated serum IgG after infection, whereas oral CT-vaccination resulted in increased levels of intestinal IgA. Neither type of vaccination successfully protected the low-responder C57 BL/10 strain and there were no effects on the low antibody levels that infection induced in this strain.
已知通过不同途径并使用不同佐剂进行疫苗接种会影响免疫反应的特征,并且可用于克服遗传决定的对感染的低反应性。利用小鼠感染肠道线虫旋毛虫的模型,研究了疫苗接种方式对高反应性(NIH)和低反应性(C57 BL/10)小鼠品系免疫反应性和蠕虫排出表型的影响。将肌肉幼虫匀浆抗原与弗氏完全佐剂(FCA)一起皮下注射以诱导全身免疫反应,或与霍乱毒素(CT)一起口服以刺激黏膜免疫。两种方法均显著保护了NIH小鼠。用FCA接种疫苗与感染后血清IgG升高相关,而口服CT疫苗接种导致肠道IgA水平升高。两种疫苗接种方式均未成功保护低反应性C57 BL/10品系,且对该品系感染诱导的低抗体水平没有影响。