EFFICACY OF ESCALATING DOSES OF LIPOSOMAL AMPHOTERICIN-B (AMBISOME) AGAINST HEMATOGENOUS CANDIDA-LUSITANIAE AND CANDIDA-KRUSEI INFECTION IN NEUTROPENIC MICE

被引:23
作者
KARYOTAKIS, NC [1 ]
ANAISSIE, EJ [1 ]
机构
[1] UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT MED SPECIALTIES,INFECT DIS SECT,HOUSTON,TX 77030
关键词
D O I
10.1128/AAC.38.11.2660
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Immunosuppressed CF1 mice were infected intravenously with two strains of Candida krusei and four strains of Candida lusitaniae (two of which were resistant to amphotericin B). Mice were treated with 1 or 2 mg of amphotericin B desoxycholate per kg of body weight per day or escalating doses of liposomal amphotericin B (8 to 30 mg/kg/day) or were left untreated, Higher doses of liposomal amphotericin B were as effective as standard dose of amphotericin B desoxycholate in prolonging survival but were significantly more effective in reducing the fungal burden in the kidneys of animals infected with both C. krusei strains and the C. lusitaniae strains that were susceptible to amphotericin B desoxycholate. This advantage of liposomal amphotericin B therapy could not be demonstrated in mice infected with the C. lusitaniae strains that were resistant to amphotericin B desoxycholate.
引用
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页码:2660 / 2662
页数:3
相关论文
共 10 条
[1]  
Adler-Moore JP., 1993, J LIPOSOME RES, V3, P429, DOI DOI 10.3109/08982109309150729
[2]   OPPORTUNISTIC MYCOSES IN THE IMMUNOCOMPROMISED HOST - EXPERIENCE AT A CANCER CENTER AND REVIEW [J].
ANAISSIE, E .
CLINICAL INFECTIOUS DISEASES, 1992, 14 :S43-S53
[3]   FLUCONAZOLE SUSCEPTIBILITY TESTING OF CANDIDA-ALBICANS - MICROTITER METHOD THAT IS INDEPENDENT OF INOCULUM SIZE, TEMPERATURE, AND TIME OF READING [J].
ANAISSIE, E ;
PAETZNICK, V ;
BODEY, GP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (08) :1641-1646
[4]   CORRELATION BETWEEN IN-VITRO AND IN-VIVO ACTIVITY OF ANTIFUNGAL AGENTS AGAINST CANDIDA SPECIES [J].
ANAISSIE, EJ ;
KARYOTAKIS, NC ;
HACHEM, R ;
DIGNANI, MC ;
REX, JH ;
PAETZNICK, V .
JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (02) :384-389
[5]   EMERGENCE OF A NEW OPPORTUNISTIC PATHOGEN, CANDIDA-LUSITANIAE [J].
BLINKHORN, RJ ;
ADELSTEIN, D ;
SPAGNUOLO, PJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (02) :236-240
[6]   AMPHOTERICIN-B LIPID COMPLEX THERAPY OF EXPERIMENTAL FUNGAL-INFECTIONS IN MICE [J].
CLARK, JM ;
WHITNEY, RR ;
OLSEN, SJ ;
GEORGE, RJ ;
SWERDEL, MR ;
KUNSELMAN, L ;
BONNER, DP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (04) :615-621
[7]   EFFICACY AND SAFETY OF AMPHOTERICIN-B COLLOIDAL DISPERSION COMPARED WITH THOSE OF AMPHOTERICIN-B DEOXYCHOLATE SUSPENSION FOR TREATMENT OF DISSEMINATED MURINE CRYPTOCOCCOSIS [J].
HOSTETLER, JS ;
CLEMONS, KV ;
HANSON, LH ;
STEVENS, DA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (12) :2656-2660
[8]   LIPOSOME-ENCAPSULATED AMPHOTERICIN-B FOR TREATMENT OF DISSEMINATED CANDIDIASIS IN NEUTROPENIC MICE [J].
LOPEZBERESTEIN, G ;
HOPFER, RL ;
MEHTA, R ;
MEHTA, K ;
HERSH, EM ;
JULIANO, RL .
JOURNAL OF INFECTIOUS DISEASES, 1984, 150 (02) :278-283
[9]   INCREASED INCIDENCE OF FUNGEMIA CAUSED BY CANDIDA-KRUSEI [J].
MERZ, WG ;
KARP, JE ;
SCHRON, D ;
SARAL, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1986, 24 (04) :581-584
[10]   EFFICACIES OF AMPHOTERICIN-B-DEOXYCHOLATE (FUNGIZONE), LIPOSOMAL AMPHOTERICIN-B (AMBISOME) AND FLUCONAZOLE IN THE TREATMENT OF SYSTEMIC CANDIDOSIS IN IMMUNOCOMPETENT AND LEUKOPENIC MICE [J].
VANETTEN, EWM ;
VANDENHEUVELDEGROOT, C ;
BAKKERWOUDENBERG, IAJM .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1993, 32 (05) :723-739