Doenhoff M J
Winches Farm Laboratories, Department of Medical Parasitology, London School of Hygiene and Tropical Medicine, St Albans, Herts., England.
Mem Inst Oswaldo Cruz. 1989 Oct;84 Suppl 1:31-7. doi: 10.1590/s0074-02761989000500004.
Experimental evidence indicates that immune effector mechanisms can enhance the activity of schistosomicidal drugs. Praziquantel, oxamniquine, hycanthone and antimony were less effective against Schistosoma mansoni infections in mice immunosuppressed by T cell-deprivation, than against comparable infections in normal mice. The schistosomicidal activities of praziquantel, oxamniquine and antimony have been experimentally enhanced by the synergistic action of immune sera. In passive serum transfer experiments a S. mansoni antigen of Mr 27kD with non-specific esterase activity was identified as a potentially sensitive target for the antibodies that interact with praziquantel. Indirect immunofluorescence indicated that this antigen was exposed on the worm surface as a result of praziquantel treatment.
实验证据表明,免疫效应机制可增强杀血吸虫药物的活性。吡喹酮、奥沙尼喹、海恩酮和锑对经T细胞去除而免疫抑制的小鼠体内曼氏血吸虫感染的疗效,低于对正常小鼠体内类似感染的疗效。吡喹酮、奥沙尼喹和锑的杀血吸虫活性已通过免疫血清的协同作用在实验中得到增强。在被动血清转移实验中,一种具有非特异性酯酶活性、分子量为27kD的曼氏血吸虫抗原被确定为与吡喹酮相互作用的抗体的潜在敏感靶点。间接免疫荧光表明,由于吡喹酮治疗,该抗原暴露于虫体表面。