INFLUENCE OF MURAMYL DIPEPTIDE ON RENAL CANDIDIASIS IN GENETICALLY DISTINCT MICE

被引:6
作者
MARQUIS, GA [1 ]
BOUSHIRA, M [1 ]
RUSSO, P [1 ]
MONTPLAISIR, S [1 ]
机构
[1] HOP ST JUSTINE,DEPT PATHOL,MONTREAL H3T 1C5,QUEBEC,CANADA
关键词
RENAL CANDIDIASIS; MURAMYL DIPEPTIDE; CANDIDA-ALBICANS; INBRED MICE; SYNTHETIC IMMUNOSTIMULANT;
D O I
10.1111/j.1699-0463.1992.tb04027.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Susceptible (DBA/2) and resistant (C57BL/6) mice were inoculated intravenously with Candida albicans to evaluate the effect of a four-day prophylaxis with muramyl dipeptide (MDP) on the renal burden of organisms during the first week after infection. In sham-treated DBA/2 mice injected with 8 x 10(4) candida cells, renal CFU (LOG10 +/- SEM) on days 1, 4 and 7 after infection were found to average 5.050 +/- 0.109, 4.882 +/- 0.133 and 5.482 +/- 0.245. In sham-treated C57BL/6 mice injected with 2 x 10(5) candida cells, renal CFU on days 1, 4 and 7 reached only 3.610 +/- 0.118, 3.404 +/- 0.107 and 4.176 +/- 0.580. MDP-treated DBA/2 mice achieved significant reduction in CFU of C. albicans on day 1 (1.3 log units) and day 4 (0.6 log unit), while MDP-treated C57BL/6 mice had significant reduction in CFU of C albicans only on day 1 (0.6 log unit) after infection. Sham-treated mice of both strains had a 28.6 to 30% increase in kidney weights on day 4 only, a transient change not seen in MDP-treated mice. Histopathological examination on days 8, 15 and 21 after infection revealed a higher incidence of renal papillary necrosis in DBA/2 mice than C57BL/6 mice (approximately 70% vs 10%). The incidence of granulomas and of chronic interstitial inflammation was much higher in MDP-treated mice. We conclude that the genetic makeup of the host influences the potential effectiveness of MDP as a biological response modifier.
引用
收藏
页码:967 / 975
页数:9
相关论文
共 28 条
  • [11] HURLEY ROSALINDE, 1963, JOUR PATH AND BACTERIOL, V86, P75, DOI 10.1002/path.1700860109
  • [12] EFFECTS OF MURAMYL DIPEPTIDE TREATMENT ON RESISTANCE TO INFECTION WITH TOXOPLASMA-GONDII IN MICE
    KRAHENBUHL, JL
    SHARMA, SD
    FERRARESI, RW
    REMINGTON, JS
    [J]. INFECTION AND IMMUNITY, 1981, 31 (02) : 716 - 722
  • [13] KUTTIN ES, 1983, SABOURAUDIA, V21, P185
  • [14] KUTTIN ES, 1983, MYKOSEN, V27, P72
  • [15] STRAIN-DEPENDENT DIFFERENCES IN SUSCEPTIBILITY OF MICE TO EXPERIMENTAL CANDIDOSIS
    MARQUIS, G
    MONTPLAISIR, S
    PELLETIER, M
    MOUSSEAU, S
    AUGER, P
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1986, 154 (05) : 906 - 909
  • [16] MASSON P, 1956, TUMEURS HUMAINES HIS, P1112
  • [17] ROLE OF COMPLEMENT DURING EXPERIMENTAL CANDIDA INFECTION IN MICE
    MORELLI, R
    ROSENBERG, LT
    [J]. INFECTION AND IMMUNITY, 1971, 3 (04) : 521 - +
  • [18] A STUDY ON RENAL PAPILLARY NECROSIS EXPERIMENTALLY PRODUCED BY THE SHWARTZMAN MECHANISM IN RABBITS
    NAKANO, F
    MORI, W
    MIYAZAKI, T
    [J]. PATHOLOGY RESEARCH AND PRACTICE, 1984, 178 (05) : 491 - 498
  • [19] EFFECT OF L18-MDP(ALA), A SYNTHETIC DERIVATIVE OF MURAMYL DIPEPTIDE, ON NONSPECIFIC RESISTANCE OF MICE TO MICROBIAL INFECTIONS
    OSADA, Y
    MITSUYAMA, M
    UNE, T
    MATSUMOTO, K
    OTANI, T
    SATOH, M
    OGAWA, H
    NOMOTO, K
    [J]. INFECTION AND IMMUNITY, 1982, 37 (01) : 292 - 300
  • [20] EFFICACY OF INTERLEUKIN-1-BETA AGAINST SYSTEMIC CANDIDA-ALBICANS INFECTIONS IN NORMAL AND IMMUNOSUPPRESSED MICE
    PECYK, RA
    FRASERSMITH, EB
    MATTHEWS, TR
    [J]. INFECTION AND IMMUNITY, 1989, 57 (10) : 3257 - 3258