Weber S M, Levitz S M, Harrison T S
Evans Memorial Department of Clinical Research, Boston University School of Medicine, Massachusetts 02118, USA.
Curr Opin Microbiol. 2000 Aug;3(4):349-53. doi: 10.1016/s1369-5274(00)00102-8.
The antimalarial drug chloroquine accumulates inside the macrophage phagolysosome by ion trapping where it exerts potent antifungal activity against Histoplasma capsulatum and Cryptococcus neoformans by distinct mechanisms. Chloroquine inhibits growth of H. capsulatum by pH-dependent iron deprivation, whereas it is directly toxic to C. neoformans. Clearly, clinical studies are required to document the potential therapeutic efficacy of chloroquine or related congeners as adjuvant therapy in fungal disease. Moreover, the diversity of pathogenic microorganisms inhibited and/or killed by chloroquine makes this drug an attractive candidate for prophylactic therapy.
抗疟药物氯喹通过离子捕获作用在巨噬细胞吞噬溶酶体内蓄积,在其中它通过不同机制对荚膜组织胞浆菌和新型隐球菌发挥强大的抗真菌活性。氯喹通过pH依赖的铁剥夺作用抑制荚膜组织胞浆菌的生长,而它对新型隐球菌具有直接毒性。显然,需要进行临床研究来证明氯喹或相关同系物作为真菌病辅助治疗的潜在疗效。此外,氯喹抑制和/或杀死的致病微生物种类多样,这使得该药物成为预防性治疗的一个有吸引力的候选药物。