National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory of Parasite and Vector Biology, Ministry of Health, WHO Collaborating Centre for Tropical Diseases, Shanghai, 200025, People's Republic of China.
Institute for Infectious Disease and Vaccine Development, Tongji University School of Medicine, Shanghai, 200092, People's Republic of China.
Infect Dis Poverty. 2018 Feb 7;7(1):9. doi: 10.1186/s40249-018-0391-x.
Chemotherapy for schistosomiasis has been around for 100 years. During the past century, great efforts have been made to develop new antischistosomal drugs from antimonials to nonantimonials, and some of these have been used extensively in clinical treatment. With the exception of a few drugs, such as oxamniquine and metrifonate, most of the antischistosomals developed in the pre-praziquantel period have variable limitations with respect to safety and efficacy. Although oxamniquine and metrifonate have been used for schistosomiasis control, they are only effective against Schistosoma mansoni and S. haematobium, respectively. Currently, praziquantel is the only drug used for treatment of all five species of human schistosomes. In this review, the pharmacological and immunological effects of praziquantel against S. japonicum are summarized and discussed.
From the end of the 1970s until the 2000s, scientists have conducted a series of experimental studies on the effects of praziquantel against S. japonicum. These have included examining its unique pharmacological action on schistosomes, the characteristics in susceptibility of the different developmental stages of schistosomes to the drug, the relationship between plasma concentration of the drug and efficacy, the impact of host factors on cidal action of the drug, prevention and early treatment of schistosomal infection, as well as praziquantel-resistant schistosomiasis.
The effects of praziquantel against S. japonicum, as elucidated by the experimental studies that are reviewed in this paper, may have some reference significance for the development of new antischistosomals.
抗血吸虫病的化学疗法已经存在了 100 年。在过去的一个世纪里,人们从抗锑药物努力开发出了许多新型抗血吸虫药物,其中一些已广泛用于临床治疗。除了少数药物(如奥沙尼喹和敌百虫)外,在前吡喹酮时期开发的大多数抗血吸虫药物在安全性和疗效方面都存在一些局限性。虽然奥沙尼喹和敌百虫曾用于血吸虫病控制,但它们分别仅对曼氏血吸虫和埃及血吸虫有效。目前,吡喹酮是唯一用于治疗所有 5 种人体血吸虫的药物。在本文中,我们总结和讨论了吡喹酮对日本血吸虫的药理学和免疫学作用。
从 20 世纪 70 年代末到 2000 年代,科学家们对吡喹酮对日本血吸虫的作用进行了一系列实验研究。这些研究包括检查其对血吸虫的独特药理作用、血吸虫不同发育阶段对药物敏感性的特征、药物血浆浓度与疗效之间的关系、宿主因素对药物杀伤作用的影响、血吸虫感染的预防和早期治疗,以及吡喹酮耐药性血吸虫病。
本文综述的实验研究阐明了吡喹酮对日本血吸虫的作用,这可能对新型抗血吸虫药物的开发具有一定的参考意义。