Dapsone as treatment adjunct in ARDS

被引:15
作者
Kast, R. E. [1 ]
机构
[1] IIAIGC Study Ctr, 148 Coll St,Suite 202D, Burlington, VT 05401 USA
关键词
ARDS; chemokine; dapsone; IL-8; RESPIRATORY-DISTRESS-SYNDROME; DIFFUSE ALVEOLAR DAMAGE; ACUTE LUNG INJURY; MONOCLONAL-ANTIBODY; RASH MITIGATION; INTERLEUKIN-8; IL-8; CIMETIDINE; CELLS; METHEMOGLOBINEMIA;
D O I
10.1080/01902148.2020.1753266
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Multiple pharmacological interventions tested over the last decades have failed to reduce ARDS mortality. This short note recounts past data indicating that (i) neutrophils home along an IL-8 gradient, (ii) in ARDS, massive neutrophil accumulation and degranulation in and along bronchoalveolar spaces contributes to damage and hypoxia, (iii) large increases in IL-8 are one of the chemotaxic signals drawing neutrophils to the ARDS lung, and (iv) old data from dermatology and glioblastoma research showed that the old drug against Hansen's disease, dapsone, inhibits neutrophils' chemotaxis to IL-8. Therefore dapsone might lower neutrophils' contributions to ARDS lung pathology. Dapsone can create methemoglobinemia that although rarely problematic it would be particularly undesirable in ARDS. The common antacid drug cimetidine lowers risk of dapsone related methemoglobinemia and should be given concomitantly.
引用
收藏
页码:157 / 161
页数:5
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