4.5 Article

5-Aminosalicylic Acid Modulates the Immune Response in Chronic Beryllium Disease Subjects

期刊

LUNG
卷 196, 期 1, 页码 103-114

出版社

SPRINGER
DOI: 10.1007/s00408-017-0062-x

关键词

Berylliosis; 5-Aminosalicylic acid; Granuloma; Lung; TNF-alpha; Therapeutic trial (or therapy); Quality of life

资金

  1. NIH [RO1 012504, RO1 ES017582, R01 ES023826, P01 ES11810]
  2. NIH/NCATS Colorado CTSA Grant from the National Center for Research Resources [UL1TR001082]

向作者/读者索取更多资源

Introduction Chronic beryllium disease (CBD) is characterized by accumulation of macrophages and beryllium-specific CD4(+) T cells that proliferate and produce Th1 cytokines. 5-Amino salicylic acid (5-ASA) is currently used to treat inflammatory bowel disease and has both antioxidant and anti-inflammatory actions. We hypothesized that 5-ASA may be a beneficial therapeutic in CBD. Methods Seventeen CBD patients were randomized 3: 1 to receive 5-ASA 500-mg capsules or placebo four times daily for 6 weeks orally. Primary study endpoints included changes in beryllium lymphocyte proliferation (BeLPT). Secondary endpoints included changes in bronchoalveolar lavage (BAL) fluid, cells, serum, and blood cell glutathione (GSH) levels, BAL cell TNF-alpha levels, lung function, and quality of life measures. Results 5-ASA decreased BAL cell BeLPT by 20% within the 5-ASA treatment group. No significant changes were observed in serum, PBMCs, BALF, or BAL cell GSH levels in either the 5-ASA or placebo treatment group. 5-ASA treatment decreased ex vivo Be-stimulated BAL cell TNF-a levels within the 5-ASA group and when compared to placebo. Significant improvements were noted in quality of life measurements with 5-ASA treatment. Conclusions 5-ASA's ability to decrease BAL cell BeLPT and Be-stimulated BAL cell TNF-a levels suggests that 5-ASA may impact the beryllium-specific immune response in CBD. 5-ASA use in other non-infectious granulomatous lung diseases, such as sarcoidosis, may prove to be a useful alternative treatment to corticosteroids for those with mild to moderate disease.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据