Anticryptococcal activity by alveolar macrophages from rats treated with cortisone acetate during different periods of time

被引:13
作者
Gross, NT
Chinchilla, M
Camner, P
Jarstrand, C
机构
[1] UNIV COSTA RICA,FAC MICROBIOL,DEPT MICROBIOL & IMMUNOL,SAN JOSE,COSTA RICA
[2] UNIV COSTA RICA,FAC MICROBIOL,DEPT PARASITOL,CIET,SAN JOSE,COSTA RICA
[3] KAROLINSKA INST,INST ENVIRONM MED,DIV INHALAT TOXICOL,S-10401 STOCKHOLM,SWEDEN
关键词
alveolar macrophages; cortisone acetate; Cryptococcus neoformans; oxidative metabolism; phagocytosis;
D O I
10.1007/BF00436653
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The effect of cortisone acetate (CA) treatment on the anticryptococcal activity by rat alveolar macrophages (AM) was investigated. The animals received a weekly dose of 5 mg CA during 1, 2, 3 or 4 weeks. Following the final dose the AM were collected by lung lavage and challenged with Cryptococcus neoformans. Parallel experiments with silica particles of a similar size were performed. The phagocytic function was assessed using a fluorescence method that distinguishes between attached and ingested particles. The oxidative metabolism was studied by the nitroblue tetrazolium (NBT) reduction test. The accumulated attachment (a measure of the attachment process) of cryptococci and silica particles per AM was significantly depressed after the third and fourth week of CA treatment. The ingested fraction (a measure of the ingestion process) of cryptococci but not of silica particles showed a small but significant decrease after the fourth week. The NET reduction of the unstimulated AM and those stimulated with either the cryptococci or silica particles for 24 h was significantly reduced after the fourth week of treatment. In conclusion, these results demonstrate that high dose CA treatment primarily affects the attachment of the cryptococci to the AM and to a lesser extent also the ingestion process. In addition, it decreases the NET reduction by AM in response to the yeast. The impairment of the AM anticryptococcal activity by high doses of CA constitutes a risk of dissemination of C. neoformans from the lungs.
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页码:1 / 8
页数:8
相关论文
共 33 条
[1]   SUBCELLULAR-DISTRIBUTION OF THE GLUCOCORTICOID RECEPTOR AND EVIDENCE FOR ITS ASSOCIATION WITH MICROTUBULES [J].
AKNER, G ;
WIKSTROM, AC ;
GUSTAFSSON, JA .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 52 (01) :1-16
[2]   DISSEMINATED CRYPTOCOCCAL DISEASE COMPLICATING STEROID-THERAPY FOR PNEUMOCYSTIS-CARINII PNEUMONIA IN A PATIENT WITH AIDS [J].
BERNSTEIN, B ;
FLOMENBERG, P ;
LETZER, D .
SOUTHERN MEDICAL JOURNAL, 1994, 87 (04) :537-538
[3]   CONTROL OF CACHECTIN (TUMOR-NECROSIS-FACTOR) SYNTHESIS - MECHANISMS OF ENDOTOXIN RESISTANCE [J].
BEUTLER, B ;
KROCHIN, N ;
MILSARK, IW ;
LUEDKE, C ;
CERAMI, A .
SCIENCE, 1986, 232 (4753) :977-980
[4]  
BOLANOS B, 1989, J MED VET MYCOL, V27, P203
[5]   CYTOKINE ENHANCEMENT OF COMPLEMENT-DEPENDENT PHAGOCYTOSIS BY MACROPHAGES - SYNERGY OF TUMOR-NECROSIS-FACTOR-ALPHA AND GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR FOR PHAGOCYTOSIS OF CRYPTOCOCCUS-NEOFORMANS [J].
COLLINS, HL ;
BANCROFT, GJ .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (06) :1447-1454
[6]   ECOLOGY, LIFE-CYCLE, AND INFECTIOUS PROPAGULE OF CRYPTOCOCCUS-NEOFORMANS [J].
ELLIS, DH ;
PFEIFFER, TJ .
LANCET, 1990, 336 (8720) :923-925
[7]   AN OVERVIEW OF MACROPHAGE-FUNGAL INTERACTIONS [J].
FROMTLING, RA ;
SHADOMY, HJ .
MYCOPATHOLOGIA, 1986, 93 (02) :77-93
[8]  
GADEBUSCH HH, 1965, AM REV RESPIR DIS, V92, P64
[9]   PATHOGENESIS OF PULMONARY CRYPTOCOCCUS-NEOFORMANS INFECTION IN THE RAT [J].
GOLDMAN, D ;
LEE, SC ;
CASADEVALL, A .
INFECTION AND IMMUNITY, 1994, 62 (11) :4755-4761
[10]  
GUDEWICZ PW, 1981, CIRC SHOCK, V8, P95