Bancroft A, Devaney E
Liverpool School of Tropical Medicine, UK.
Parasite Immunol. 1993 Mar;15(3):153-62. doi: 10.1111/j.1365-3024.1993.tb00595.x.
BALB/c mice immunized with L3 of Brugia pahangi, irradiated at 45 kRad from a 137Caesium source, are strongly immune to challenge infection (75-100% reduction in the recovery of challenge infection larvae on day 6 post-challenge). The target of immunity appears to be the post-infective L3, as challenge infection larvae are killed within 5-6 days of infection. By immunoblot analysis, serum from immune animals recognizes a limited set of somatic antigens, the majority of which are shared between different life cycle stages. Serum from immune mice also strongly recognizes larval surface antigens by immunofluorescence, some of which may be stage specific. The larval surface determinants do not appear to be protein or glycoprotein by standard immunochemical analysis. A proportion of the antibody response of the BALB/c mouse is directed towards phosphorylcholine epitopes on filarial antigens, but the limited antigen recognition cannot be explained on the basis of the mouse strain used, as CBA/Ca mice recognize a similar limited set of antigens.
用来自铯 - 137源、经45千拉德辐照的彭亨布鲁线虫L3免疫的BALB/c小鼠,对攻击感染具有很强的免疫力(攻击感染后第6天,攻击感染幼虫的回收率降低75 - 100%)。免疫的靶标似乎是感染后的L3,因为攻击感染的幼虫在感染后5 - 6天内被杀死。通过免疫印迹分析,免疫动物的血清识别一组有限的体细胞抗原,其中大多数在不同生命周期阶段之间共享。免疫小鼠的血清通过免疫荧光也强烈识别幼虫表面抗原,其中一些可能是阶段特异性的。通过标准免疫化学分析,幼虫表面决定簇似乎不是蛋白质或糖蛋白。BALB/c小鼠的一部分抗体反应针对丝虫抗原上的磷酸胆碱表位,但有限的抗原识别不能基于所用的小鼠品系来解释,因为CBA/Ca小鼠识别一组类似的有限抗原。