Rees R J, Pearson J M, Waters M F
Br Med J. 1970 Jan 10;1(5688):89-92. doi: 10.1136/bmj.1.5688.89.
Rifampicin showed high activity against experimental leprosy, inhibiting the multiplication of dapsone-sensitive and dapsone-resistant strains of Mycobacterium leprae in mice fed 5 mg./kg. body weight. In a formal pilot-type trial on six previously untreated patients with active lepromatous leprosy, rifampicin (600 mg. daily by mouth) was as effective as standard treatment with dapsone. Myco. leprae, however, appeared to be killed more rapidly by rifampicin than by dapsone or other antileprosy drugs so far studied. This was confirmed on a further 10 patients, including two with dapsone resistance, and from the infectivity in mice of bacilli recovered from patients during treatment with rifampicin or dapsone. These results are consistent with the bactericidal activity of rifampicin against other micro-organisms, which could be important to the chemotherapy of leprosy, since all antileprosy drugs in current use are bacteriostatic.
利福平对实验性麻风表现出高活性,在给体重5毫克/千克的小鼠喂食时,可抑制敏感和耐氨苯砜的麻风分枝杆菌菌株的繁殖。在一项针对6名先前未经治疗的活动性瘤型麻风患者的正式试点试验中,利福平(每日口服600毫克)与氨苯砜标准治疗效果相当。然而,与氨苯砜或迄今研究的其他抗麻风药物相比,利福平似乎能更快地杀死麻风分枝杆菌。在另外10名患者(包括2名耐氨苯砜患者)身上得到了证实,这是根据利福平或氨苯砜治疗期间从患者身上分离出的杆菌在小鼠中的传染性得出的。这些结果与利福平对其他微生物的杀菌活性一致,这对麻风化疗可能很重要,因为目前使用的所有抗麻风药物都是抑菌性的。