Zafra R, Pérez-Écija R A, Buffoni L, Moreno P, Bautista M J, Martínez-Moreno A, Mulcahy G, Dalton J P, Pérez J
Animal Health Institute (IUSA), University of Las Palmas de Gran Canaria, Campus Trasmontaña, Aurcas, Spain.
J Comp Pathol. 2013 May;148(4):373-84. doi: 10.1016/j.jcpa.2012.08.007. Epub 2012 Oct 16.
The aim of the present study was to study peritoneal and hepatic changes during early [7-9 days postinfection (dpi)] and late [15 weeks postinfection (wpi)] infection of goats immunized with recombinant F. hepatica pro cathepsin L1 (rCL1) in Quil A and challenged with Fasciola hepatica. Despite finding no significant reduction in fluke burdens between the control and immunized group, at 15 dpi the rCL1-vaccinated group showed significantly higher weight gain and reduced severity of hepatic lesions compared with the control group that received only Quil A. In the rCL1-vaccinated group, two of three goats sacrificed at 7-9 dpi had little hepatic damage and had a higher percentage of peritoneal eosinophils and elevated induced nitric oxide synthase (iNOS) expression in peritoneal cells than the goats from the control group. Moreover, while these two goats showed a heavy infiltration of eosinophils surrounding migrating flukes, the remaining animals examined at 7-9 dpi had no inflammatory infiltration surrounding migrating flukes. Two out of seven goats in the rCL1-vaccinated group had low fluke burdens and little hepatic damage at 15 wpi, suggesting an effective protective response in some of the vaccinated goats. This protective response did not correlate with peripheral eosinophilia or with serum titres of anti-rCL1 immunoglobulin (Ig) G. The results of the present work suggest that an eosinophil-mediated immune response plays a crucial role in the early effective host response against F. hepatica in goats. Adjuvants designed to increase cell-mediated immunity should be tested in future vaccine trials against F. hepatica.
本研究的目的是研究在第7 - 9天感染后早期(dpi)和第15周感染后晚期(wpi),用重组肝片吸虫组织蛋白酶L1(rCL1)在Quil A中免疫并受到肝片吸虫攻击的山羊的腹膜和肝脏变化。尽管在对照组和免疫组之间未发现吸虫负荷有显著降低,但在感染后15天,与仅接受Quil A的对照组相比,接种rCL1的组体重增加显著更高,肝脏病变严重程度降低。在接种rCL1的组中,在7 - 9 dpi处死的三只山羊中有两只肝脏损伤较小,腹膜嗜酸性粒细胞百分比更高,腹膜细胞中诱导型一氧化氮合酶(iNOS)表达升高,高于对照组山羊。此外,虽然这两只山羊显示迁移吸虫周围有大量嗜酸性粒细胞浸润,但在7 - 9 dpi检查的其余动物在迁移吸虫周围没有炎症浸润。接种rCL1的组中七只山羊中有两只在15 wpi时吸虫负荷低且肝脏损伤小,表明一些接种疫苗的山羊有有效的保护性反应。这种保护性反应与外周嗜酸性粒细胞增多或抗rCL1免疫球蛋白(Ig)G的血清滴度无关。本研究结果表明,嗜酸性粒细胞介导的免疫反应在山羊对肝片吸虫的早期有效宿主反应中起关键作用。旨在增强细胞介导免疫的佐剂应在未来针对肝片吸虫的疫苗试验中进行测试。