Proinflammatory activity in bronchoalveolar lavage fluids from patients with ARDS, a prominent role for interleukin-1

被引:263
作者
Pugin, J
Ricou, B
Steinberg, KP
Suter, PM
Martin, TR
机构
[1] UNIV HOSP GENEVA,DEPT ANESTHESIOL PHARMACOL & SURG INTENS CARE,DIV SURG INTENS CARE,CH-1211 GENEVA 14,SWITZERLAND
[2] UNIV WASHINGTON,HARBORVIEW MED CTR,SEATTLE,WA 98104
[3] VET AFFAIRS MED CTR,SEATTLE,WA 98108
关键词
D O I
10.1164/ajrccm.153.6.8665045
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Proinflammatory cytokines such as tumor necrosis factor-alpha (TNF) and interleukin-1 beta (IL-1) have been found to be elevated in bronchoalveolar lavage (BAL) fluid and in plasma from patients with acute respiratory distress syndrome (ARDS). In order to measure the balance of proinflammatory cytokines and their inhibitors, we quantified the upregulation of intercellular adhesion molecule-1 (ICAM-1) induced by ARDS BAL fluids in human alveolar type II-like (A459) cells, and defined proinflammatory activity as the amount of ICAM-1 induced by the BAL fluids. Proinflammatory activity was detected in 77% of the BAL fluids sampled during the first week of ARDS, was found maximal during the 3 first days after onset of ARDS, and was significantly greater than in BAL specimens from ''at risk'' patients. Blocking experiments with specific inhibitors of TNF and IL-1 added to the BAL fluids Indicated that the bioactivity measured was mainly due to IL-1. In contrast, proinflammatory activity of conditioned supernates from endotoxin-treated alveolar macrophages was mostly due to TNF. Using a bioassay that measures balance of cytokines with their inhibitors, our results indicate that the net proinflammatory activity in ARDS BAL fluids is attributable to IL-1 and not to TNF.
引用
收藏
页码:1850 / 1856
页数:7
相关论文
共 31 条
[1]   PURIFICATION OF TYPE-I AND TYPE-II TUMOR-NECROSIS-FACTOR RECEPTORS FROM HUMAN LUNG-TISSUE [J].
ABDOLRASULNIA, R ;
SHEPHERD, VL .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 7 (01) :42-48
[2]  
ARNOLD R, 1994, IMMUNOLOGY, V82, P126
[3]   ALVEOLAR TYPE-II EPITHELIAL-CELLS PRODUCE INTERLEUKIN-6 IN-VITRO AND IN-VIVO - REGULATION BY ALVEOLAR MACROPHAGE SECRETORY PRODUCTS [J].
CRESTANI, B ;
CORNILLET, P ;
DEHOUX, M ;
ROLLAND, C ;
GUENOUNOU, M ;
AUBIER, M .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (02) :731-740
[4]  
DINARELLO CA, 1991, BLOOD, V77, P1627
[5]   INTERLEUKIN-8 AND DEVELOPMENT OF ADULT RESPIRATORY-DISTRESS SYNDROME IN AT-RISK PATIENT GROUPS [J].
DONNELLY, SC ;
STRIETER, RM ;
KUNKEL, SL ;
WALZ, A ;
ROBERTSON, CR ;
CARTER, DC ;
GRANT, IS ;
POLLOK, AJ ;
HASLETT, C .
LANCET, 1993, 341 (8846) :643-647
[6]   A HIGHLY SENSITIVE CELL-LINE, WEHI-164 CLONE 13, FOR MEASURING CYTOTOXIC FACTOR TUMOR-NECROSIS-FACTOR FROM HUMAN-MONOCYTES [J].
ESPEVIK, T ;
NISSENMEYER, J .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 95 (01) :99-105
[7]   ADULT RESPIRATORY-DISTRESS SYNDROME - RISK WITH COMMON PREDISPOSITIONS [J].
FOWLER, AA ;
HAMMAN, RF ;
GOOD, JT ;
BENSON, KN ;
BAIRD, M ;
EBERLE, DJ ;
PETTY, TL ;
HYERS, TM .
ANNALS OF INTERNAL MEDICINE, 1983, 98 (05) :593-597
[8]   TUMOR-NECROSIS-FACTOR LEVELS IN SERUM AND BRONCHOALVEOLAR LAVAGE FLUID OF PATIENTS WITH THE ADULT RESPIRATORY-DISTRESS SYNDROME [J].
HYERS, TM ;
TRICOMI, SM ;
DETTENMEIER, PA ;
FOWLER, AA .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1991, 144 (02) :268-271
[9]   ELEVATED INTERLEUKIN-1 RELEASE BY HUMAN ALVEOLAR MACROPHAGES DURING THE ADULT RESPIRATORY-DISTRESS SYNDROME [J].
JACOBS, RF ;
TABOR, DR ;
BURKS, AW ;
CAMPBELL, GD .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 140 (06) :1686-1692
[10]  
MATTHAY MA, 1990, CLIN CHEST MED, V11, P575