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

促炎细胞因子 急性呼吸窘迫综合征 支气管肺泡灌洗 医学 肿瘤坏死因子α 免疫学 炎症 白细胞介素 白细胞介素8 白细胞介素6 败血症 急性呼吸窘迫 细胞因子 内科学
作者
Jérôme Pugin,Bara Ricou,Kenneth P. Steinberg,Peter M. Suter,Thomas R. Martin
出处
期刊:American Journal of Respiratory and Critical Care Medicine [American Thoracic Society]
卷期号:153 (6): 1850-1856 被引量:298
标识
DOI:10.1164/ajrccm.153.6.8665045
摘要

Proinflammatory cytokines such as tumor necrosis factor-alpha (TNF) and interleukin-1beta (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 molecules (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 SAL fluids. Proinflammatory activity was detected in 77% of the SAL 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.

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