Chance M L
Liverpool School of Tropical Medicine, U.K.
Ann Trop Med Parasitol. 1995 Dec;89 Suppl 1:37-43. doi: 10.1080/00034983.1995.11813013.
Several significant advances in the chemotherapy of leishmaniasis have occurred in the last 10 years. Some of these advances have arisen due to the greater awareness of the pharmacokinetic properties of drugs, such as the pentavalent antimonials, while others have resulted from the introduction of drugs new to the treatment of leishmaniasis, such as aminosidine which can be used both systemically and topically against cutaneous leishmaniasis. The most encouraging advance is the use of lipid-associated amphotericin B; very short treatments with these preparations have been shown to be effective. Other studies have shown the usefulness of combination therapy and the use of immune modulators. A number of biochemical pathways in Leishmania, such as those associated with purine and sterol metabolism, are known to be distinct from those of the mammalian hosts. These have been exploited in the search for the rational choice of anti-leishmanial agents.
过去10年里,利什曼病化疗取得了几项重大进展。其中一些进展是由于对药物(如五价锑)药代动力学特性有了更深入的认识,而其他进展则是因为引入了治疗利什曼病的新药,如可全身和局部用于治疗皮肤利什曼病的氨基糖苷。最令人鼓舞的进展是使用脂质体两性霉素B;已证明用这些制剂进行极短疗程的治疗是有效的。其他研究表明联合治疗和使用免疫调节剂也很有用。已知利什曼原虫中的一些生化途径,如与嘌呤和甾醇代谢相关的途径,与哺乳动物宿主的生化途径不同。这些已被用于合理选择抗利什曼原虫药物的研究中。