Tumor necrosis factor (TNF) induction from monocyte/macrophages by Candida species

被引:23
作者
Aybay, C [1 ]
Imir, T [1 ]
机构
[1] GAZI UNIV,SCH MED,DEPT MICROBIOL & IMMUNOL,TR-06500 BESEVLER,ANKARA,TURKEY
关键词
D O I
10.1016/S0171-2985(96)80059-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Candida albicans was studied for its capacity to induce TNF production from mouse peritoneal macrophages (PM Phi). TNF activities in the culture supernatants of candida-stimulated PM Phi and human peripheral blood monocytes were assessed by L 929 bioassay and ELISA respectively. C. albicans induced TNF production from PM Phi and human peripheral blood monocytes in a dose-dependent manner. Although the capacity was lesser than live form, heat-killed C. albicans was also found to be capable of stimulating PM Phi, to induce TNF. The filtered supernatant of 24 h cultured live C. albicans had no effect on TNF production from PM Phi. Saccharomyces cerevisiae-extracted mannan, a yeast cell wall antigen, induced TNF production from PM Phi, in a dose-dependent manner. Thus, the effect of C. albicans on TNF production from PM Phi was seemed to be directly related to the presence of the yeast cell wall itself. Compatible with these data, when various candida species (C. albicans, C. tropicalis, C. pseudotropicalis. C. lusitaniae, C. krusei, C. parapsilosis, C. guilliermondii, C. stellatoidea, C. glabrata) and S. cerevisiae were compared to each other, at a concentration of 2x10(6) yeast cells/ml from each species, it was observed that TNF inducing capacities varied. Among the species used in this study, C, guilliermondii and C. glabrata, of which the yeast cell size were the smallest ones, were found to be less potent than that of others to induce TNF from PM Phi.
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页码:363 / 374
页数:12
相关论文
共 46 条
[1]   INDUCTION OF TUMOR-NECROSIS-FACTOR-ALPHA IN MURINE CANDIDA-ALBICANS INFECTION [J].
ALLENDOERFER, R ;
MAGEE, DM ;
SMITH, JG ;
BONEWALD, L ;
GRAYBILL, JR .
JOURNAL OF INFECTIOUS DISEASES, 1993, 167 (05) :1168-1172
[2]   THE EFFECT OF OMEPRAZOLE ON HUMAN NATURAL-KILLER-CELL ACTIVITY [J].
AYBAY, C ;
IMIR, T ;
OKUR, H .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1995, 26 (06) :1413-1418
[3]   CACHECTIN AND TUMOR-NECROSIS-FACTOR AS 2 SIDES OF THE SAME BIOLOGICAL COIN [J].
BEUTLER, B ;
CERAMI, A .
NATURE, 1986, 320 (6063) :584-588
[4]   PASSIVE-IMMUNIZATION AGAINST CACHECTIN TUMOR NECROSIS FACTOR PROTECTS MICE FROM LETHAL EFFECT OF ENDOTOXIN [J].
BEUTLER, B ;
MILSARK, IW ;
CERAMI, AC .
SCIENCE, 1985, 229 (4716) :869-871
[5]  
BEUTLER B, 1989, ANNU REV IMMUNOL, V7, P625, DOI 10.1146/annurev.iy.07.040189.003205
[6]  
BURCHARD KW, 1983, ARCH SURG-CHICAGO, V118, P217
[7]  
CASWELL EA, 1975, P NATL ACAD SCI USA, V72, P3666
[8]   PUTATIVE VIRULENCE FACTORS OF CANDIDA-ALBICANS [J].
CUTLER, JE .
ANNUAL REVIEW OF MICROBIOLOGY, 1991, 45 :187-218
[9]  
DJEU JY, 1988, J IMMUNOL, V141, P4047
[10]   SEPARATION OF IMMUNOMODULATORY EFFECTS OF MANNAN FROM CANDIDA-ALBICANS INTO STIMULATORY AND SUPPRESSIVE COMPONENTS [J].
DOMER, JE ;
STASHAK, PW ;
ELKINS, K ;
PRESCOTT, B ;
CALDES, G ;
BAKER, PJ .
CELLULAR IMMUNOLOGY, 1986, 101 (02) :403-414