Fallon P G, Doenhoff M J
School of Biological Sciences, University of Wales, Bangor, UK.
Parasite Immunol. 1995 May;17(5):261-8. doi: 10.1111/j.1365-3024.1995.tb01024.x.
The efficacy of praziquantel treatment was significantly enhanced (P < 0.01) in CBA/Ca mice that had been immunized prior to Schistosoma mansoni infection with a crude extract of worm membrane antigens. In Western immunoblots sera from the worm antigen-immunized animals had a polyspecific antibody response, with a 25-27 kDa antigen being reacted against with particular intensity. A molecule of similar size was also recognized by rabbit antisera raised against an antigen with esterase activity that has been previously identified as a sensitive target for drug-antibody synergy. The increase in efficacy of subcurative doses of praziquantel in immunized animals is attributed to drug-induced tegumental damage causing antigens to become exposed on the worm surface. Thus, specific antigens, including the 25-27 kDa antigen, become accessible to circulating schistosomicidal antibodies. The role of antibodies that can synergize with praziquantel to kill schistosome worms is discussed.
在用曼氏血吸虫感染之前用虫膜抗原粗提物免疫过的CBA/Ca小鼠中,吡喹酮治疗的疗效显著增强(P < 0.01)。在Western免疫印迹中,来自经虫抗原免疫动物的血清呈现多特异性抗体反应,其中一种25 - 27 kDa的抗原反应尤为强烈。针对一种具有酯酶活性的抗原制备的兔抗血清也识别出了一个大小相似的分子,该抗原先前已被确定为药物 - 抗体协同作用的敏感靶点。免疫动物中次治疗剂量吡喹酮疗效的提高归因于药物诱导的体表损伤,导致抗原暴露于虫体表面。因此,包括25 - 27 kDa抗原在内的特定抗原可被循环中的杀血吸虫抗体识别。本文还讨论了可与吡喹酮协同作用以杀死血吸虫的抗体的作用。