Effects after inhalation of (1→3)-β-D-glucan in healthy humans

被引:44
作者
Thorn, J [1 ]
Beijer, L [1 ]
Rylander, R [1 ]
机构
[1] Univ Gothenburg, Dept Environm Med, S-40530 Gothenburg, Sweden
关键词
(1 -> 3)-beta-D-glucan; inflammatory markers; cytokines; induced sputum;
D O I
10.1080/09629350124119
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background and aim: This study was performed to assess the effects of an exposure to a pure (1 -->3)-beta -D-glucan, a cell wall component of fungi, plants and certain bacteria. Methods: Twenty-one healthy subjects inhaled saline or (1 -->3)-beta -D-glucan suspended in saline in a random, double-blind, cross-over design. They were examined before exposure and 24 and 72 h afterwards with spirometry, blood sampling and collection of induced sputum. Differential cell counts and eosinophilic cationic protein (ECP) were determined in blood and sputum, and myeloperoxidase (MPO), tumour necrosis factor-alpha (TNF-alpha), and interleukin (IL)-8 and IL-10 were determined in sputum supernatants. TNF-alpha was determined after cultivation of blood mononuclear cells. Results: In sputum, inhalation of saline caused a significant increase in ECP and TNF-alpha. (1 -->3)-beta -D-Glucan inhalation caused a further increase in these cytokines, although not statistically significantly different from the increase induced by inhalation of saline alone. in blood, the number of eosinophils was significantly decreased 72 h after the challenge with (1 -->3)-beta -D-glucan. This effect was not found after the inhalation of saline alone. TNF-alpha production from stimulated blood mononuclear cells was significantly decreased 72 h after the (1 -->3)-beta -D-glucan Inhalation as compared with the increase induced by saline inhalation. Conclusions: The results suggest that (1 -->3)-beta -D-glucan causes a different type of response as compared with inflammatory agents such as bacterial endotoxin that cause a neutrophil-dominated inflammatory response.
引用
收藏
页码:173 / 178
页数:6
相关论文
共 31 条
[11]  
KNUDSON RJ, 1983, AM REV RESPIR DIS, V127, P725
[12]   THE USE OF PHADIATOP IN MASS-SCREENING PROGRAMS OF INHALANT ALLERGIES - ADVANTAGES AND LIMITATIONS [J].
MATRICARDI, PM ;
NISINI, R ;
PIZZOLO, JG ;
DAMELIO, R .
CLINICAL AND EXPERIMENTAL ALLERGY, 1990, 20 (02) :151-155
[13]   INFLAMMATORY RESPONSE TO ACUTE INHALATION OF ENDOTOXIN IN ASTHMATIC-PATIENTS [J].
MICHEL, O ;
GINANNI, R ;
LEBON, B ;
CONTENT, J ;
DUCHATEAU, J ;
SERGYSELS, R .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 146 (02) :352-357
[14]   Dose-response relationship to inhaled endotoxin in normal subjects [J].
Michel, O ;
Nagy, AM ;
Schroeven, M ;
Duchateau, J ;
Neve, J ;
Fondu, P ;
Sergysels, R .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 156 (04) :1157-1164
[15]   USE OF INDUCED SPUTUM CELL COUNTS TO INVESTIGATE AIRWAY INFLAMMATION IN ASTHMA [J].
PIN, I ;
GIBSON, PG ;
KOLENDOWICZ, R ;
GIRGISGABARDO, A ;
DENBURG, JA ;
HARGREAVE, FE ;
DOLOVICH, J .
THORAX, 1992, 47 (01) :25-29
[16]  
PRETUS HA, 1991, J PHARMACOL EXP THER, V257, P500
[17]   Airways inflammation among workers in a paper industry [J].
Rylander, R ;
Thorn, J ;
Attefors, R .
EUROPEAN RESPIRATORY JOURNAL, 1999, 13 (05) :1151-1157
[18]  
Rylander R., 1997, INT J OCCUP ENV HEAL, V3, pS1, DOI 10.1179/oeh.1997.3.1.1.
[19]  
RYLANDER R, 1993, P AM SOC HEAT REFR A, P338
[20]  
RYLANDER R, 1996, INDOOR BUILT ENVIRON, V5, P106