Comparative antifungal activities and plasma pharmacokinetics of micafungin (FK463) against disseminated candidiasis and invasive pulmonary aspergillosis in persistently neutropenic rabbits

被引:142
作者
Petraitis, V
Petraitiene, R
Groll, AH
Roussillon, K
Hemmings, M
Lyman, CA
Sein, T
Bacher, J
Bekersky, I
Walsh, TJ
机构
[1] NCI, Immunocompromised Host Sect, Pediat Oncol Branch, NIH, Bethesda, MD 20892 USA
[2] NIH, Warren Grant Magnuson Clin Ctr, Vet Resources Program, Off Res Serv, Bethesda, MD 20892 USA
[3] NIH, Surg Serv, Vet Resources Program, Off Res Serv, Bethesda, MD 20892 USA
[4] Fujisawa Healthcare Inc, Deerfield, IL USA
关键词
D O I
10.1128/AAC.46.6.1857-1869.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Micafungin (FK463) is an echinocandin that demonstrates potent in vitro antifungal activities against Candida and Aspergillus species. However, little is known about its comparative antifungal activities in persistently neutropenic hosts. We therefore investigated the plasma micafungin pharmacokinetics and antifungal activities of micafungin against experimental disseminated candidiasis and invasive pulmonary aspergillosis in persistently neutropenic rabbits. The groups with disseminated candidiasis studied consisted of untreated controls (UCs); rabbits treated with desoxycholate amphotericin B (DAMB) at 1 mg/kg of body weight/day; or rabbits treated with micafungin at 0.25, 0.5, 1, and 2 mg/kg/day intravenously. Compared with the UCs, rabbits treated with micafungin or DAMB showed significant dosage-dependent clearance of Candida albicans from the liver, spleen, kidney, brain, eye, lung, and vena cava. These in vivo findings correlated with the results of in vitro time-kill assays that demonstrated that micafungin has concentration-dependent fungicidal activity. The groups with invasive pulmonary aspergillosis studied consisted of UCs; rabbits treated with DAMB; rabbits treated with liposomal amphotericin B (LAMB) at 5 mg/kg/day; and rabbits treated with micafungin at 0.5, 1, and 2 mg/kg/day. In comparison to the significant micafungin dosage-dependent reduction of the residual burden (in log CFU per gram) of C. albicans in tissue, micafungin-treated rabbits with invasive pulmonary aspergillosis had no reduction in the concentration of Aspergillus fumigatus in tissue. DAMB and LAMB significantly reduced the burdens of C. albicans and A. fumigatus in tissues (P < 0.01). Persistent galactomannan antigenemia in micafungin-treated rabbits correlated with the presence of an elevated burden of A. fumigatus in pulmonary tissue. By comparison, DAMB- and LAMB-treated animals had significantly reduced circulating galactomannan antigen levels. Despite a lack of clearance of A. fumigatus from the lungs, there was a significant improvement in the rate of survival (P < 0.001) and a reduction in the level of pulmonary infarction (P < 0.05) in micafungin-treated rabbits. In summary, micafungin demonstrated concentration-dependent and dosage-dependent clearance of C albicans from persistently neutropenic rabbits with disseminated candidiasis but not of A. fumigatus from persistently neutropenic rabbits with invasive pulmonary aspergillosis.
引用
收藏
页码:1857 / 1869
页数:13
相关论文
共 44 条
  • [11] GROLL A, IN PRESS INFECT DIS
  • [12] Compartmental pharmacokinetics and tissue distribution of the antifungal echinocandin lipopeptide micafungin (FK463) in rabbits
    Groll, AH
    Mickiene, D
    Petraitis, V
    Petraitiene, R
    Ibrahim, KH
    Piscitelli, SC
    Bekersky, I
    Walsh, TJ
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (12) : 3322 - 3327
  • [13] Trends in the postmortem epidemiology of invasive fungal infections at a university hospital
    Groll, AH
    Shah, PM
    Mentzel, C
    Schneider, M
    JustNuebling, G
    Huebner, K
    [J]. JOURNAL OF INFECTION, 1996, 33 (01) : 23 - 32
  • [14] GROLL AH, 2000, CURR OPIN ANTIINFECT, V2, P405
  • [15] Efficacy of FK463, a new lipopeptide antifungal agent, in mouse models of disseminated candidiasis and aspergillosis
    Ikeda, F
    Wakai, Y
    Matsumoto, S
    Maki, K
    Watabe, E
    Tawara, S
    Goto, T
    Watanabe, Y
    Matsumoto, F
    Kuwahara, S
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (03) : 614 - 618
  • [16] Evaluation of endpoints for antifungal susceptibility determinations with LY303366
    Klepser, ME
    Ernst, EJ
    Ernst, ME
    Messer, SA
    Pfaller, MA
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (06) : 1387 - 1391
  • [17] MORPHOLOGICAL EFFECTS OF LIPOPEPTIDES AGAINST ASPERGILLUS-FUMIGATUS CORRELATE WITH ACTIVITIES AGAINST (1,3)-BETA-D-GLUCAN SYNTHASE
    KURTZ, MB
    HEATH, IB
    MARRINAN, J
    DREIKORN, S
    ONISHI, J
    DOUGLAS, C
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (07) : 1480 - 1489
  • [18] PHARMACOKINETICS AND SAFETY OF A UNILAMELLAR LIPOSOMAL FORMULATION OF AMPHOTERICIN-B (AMBISOME) IN RABBITS
    LEE, JW
    AMANTEA, MA
    FRANCIS, PA
    NAVARRO, EE
    BACHER, J
    PIZZO, PA
    WALSH, TJ
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (04) : 713 - 718
  • [19] Efficacy of FK463, a (1,3)-β-D-glucan synthase inhibitor, in disseminated azole-resistant Candida albicans infection in mice
    Maesaki, S
    Hossain, MA
    Miyazaki, Y
    Tomono, K
    Tashiro, T
    Kohno, S
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (06) : 1728 - 1730
  • [20] Efficacy of FK463, a new lipopeptide antifungal agent, in mouse models of pulmonary aspergillosis
    Matsumoto, S
    Wakai, Y
    Nakai, T
    Hatano, K
    Ushitani, T
    Ikeda, F
    Tawara, S
    Goto, T
    Matsumoto, F
    Kuwahara, H
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (03) : 619 - 621