Mefloquine is active in vitro and in vivo against Mycobacterium avium complex

被引:71
作者
Bermudez, LE
Kolonoski, P
Wu, M
Aralar, PA
Inderlied, CB
Young, LS
机构
[1] Kuzell Inst Arthrit & Infect Dis, San Francisco, CA 94115 USA
[2] Univ So Calif, Childrens Hosp Los Angeles, Dept Pathol & Lab Med, Los Angeles, CA USA
关键词
D O I
10.1128/AAC.43.8.1870
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Despite the development of several agents, new classes of antimicrobials with activity against the Mycobacterium avium complex (MAC) are needed. Based on a broad screening of compounds, we found that mefloquine has MICs of 8 to 16 mu g/ml by the BACTEC system and 16 mu g/ml by broth microdilution for five MAC strains tested, An expansion of the screening with broth microdilution to 24 macrolide-susceptible strains and 6 macrolide-resistant strains determined that the MIC for all strains was 16 mu g/ml. To determine the intracellular activity of mefloquine, U937 macrophage monolayers infected with MAC strain 101, 100, or 109 (serovars 1, 8, and 4) were treated with mefloquine daily, and the number of intracellular bacteria was quantitated after 4 days. Significant growth inhibition against the three MAC strains at concentrations greater than or equal to 10 mu g/ml (P < 0.05) was obtained. Due to the encouraging anti-MAC activity, in vivo efficacy in beige mice infected with MAC 101 was evaluated. Animals were treated with 5, 10, 20, or 40 mg/kg of body weight daily, three times a week, twice a week, or once a week for 4 weeks, and bacteria were quantitated in blood, liver, and spleen, No toxicity was observed with any of the treatment regimens. Mefloquine had borderline bactericidal activity at a dosage of 40 mg/kg daily (100% inhibition compared with a 1-week control), and significant inhibition was obtained at dosages of 40 mg/kg three times a week, as well as 20 mg/kg daily. Mefloquine had no significant effect on bacteremia, A combination of mefloquiue and ethambutol showed significantly more activity than did either drug alone in liver, spleen, and blood; the combination was also bactericidal against M, avium. Although safety is a potential concern, mefloquine and related compounds deserve further investigation as anti-MAC therapies.
引用
收藏
页码:1870 / 1874
页数:5
相关论文
共 21 条
[1]   New drugs for the therapy of mycobacterial infections [J].
Bermudez, LE ;
Young, LS .
CURRENT OPINION IN INFECTIOUS DISEASES, 1995, 8 (06) :428-437
[2]   Activities of Bay Y 3118, levofloxacin, and ofloxacin alone or in combination with ethambutol against Mycobacterium avium complex in vitro, in human macrophages, and in beige mice [J].
Bermudez, LE ;
Inderlied, CB ;
Kolonoski, P ;
Wu, M ;
BarbaraBurnham, L ;
Young, LS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (03) :546-551
[3]   CLARITHROMYCIN, DAPSONE, AND A COMBINATION OF BOTH USED TO TREAT OR PREVENT DISSEMINATED MYCOBACTERIUM-AVIUM INFECTION IN BEIGE MICE [J].
BERMUDEZ, LE ;
INDERLIED, CB ;
KOLONOSKI, P ;
PETROFSKY, M ;
YOUNG, LS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (12) :2717-2721
[4]   Emergence of Mycobacterium avium populations resistant to macrolides during experimental chemotherapy [J].
Bermudez, LE ;
Petrofsky, M ;
Kolonoski, P ;
Young, LS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (01) :180-183
[5]  
BERMUDEZ LE, 1988, J IMMUNOL, V9, P3006
[6]   CLARITHROMYCIN THERAPY FOR BACTEREMIC MYCOBACTERIUM-AVIUM COMPLEX DISEASE - A RANDOMIZED, DOUBLE-BLIND, DOSE-RANGING STUDY IN PATIENTS WITH AIDS [J].
CHAISSON, RE ;
BENSON, CA ;
DUBE, MP ;
HEIFETS, LB ;
KORVICK, JA ;
ELKIN, S ;
SMITH, T ;
CRAFT, JC ;
SATTLER, FR ;
STOOL, EW ;
MACGREGOR, RR ;
BUEHNER, T ;
WU, AW ;
BARNES, GL ;
BECKER, R ;
URBANSKI, P ;
RICHARDSON, W ;
HAFNER, R ;
DIXON, D ;
FEIGAL, DW ;
DELLERSON, M ;
GUPTA, S ;
HENRY, D ;
SCHLAGER, S .
ANNALS OF INTERNAL MEDICINE, 1994, 121 (12) :905-911
[7]   Side effects of mefloquine prophylaxis for malaria: An independent randomized controlled trial [J].
Croft, AMJ ;
Clayton, TC ;
World, MJ .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1997, 91 (02) :199-203
[8]  
DESNEVES J, 1996, MOL BIOCHEM PARASIT, V82, P182
[9]   Epidemiology of infection by nontuberculous mycobacteria [J].
Falkinham, JO .
CLINICAL MICROBIOLOGY REVIEWS, 1996, 9 (02) :177-+
[10]   Quinoline antimalarials: Mechanisms of action and resistance and prospects for new agents [J].
Foley, M ;
Tilley, L .
PHARMACOLOGY & THERAPEUTICS, 1998, 79 (01) :55-87