FK506 inhibition of histamine release and cytokine production by mast cells and basophils

T. Sengoku, S. Kishi, S. Sakuma, Y. Ohkubo, T. Goto
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引用次数: 41

Abstract

Histamine release and cytokine production by mast cells and basophils are thought to be closely involved in the pathogenesis of allergic diseases. Some reports show that FK506 (tacrolimus hydrate) inhibited histamine release and cytokine production by mast cells and basophils. However, as the effects of FK506 has not been compared with those of clinically used drugs in those reports, the clinical relevancy of FK506 inhibition remained unclear. In this paper, we compared the actions of FK506 with those of steroids or disodium cromoglycate (DSCG) which has been clinically used. FK506 inhibited histamine release by Brown–Norway rat peritoneal mast cells more potently than steroids and especially DSCG. FK506 also inhibited histamine release by a mast rat basophilic leukemia (RBL)-1 cell line and human peripheral blood basophils, whereas steroids failed to inhibit histamine release by human basophils. FK506 as well as steroids inhibited TNF-α and IL-4 production by RBL-1 cells. FK506 was therefore more effective than steroids and DSCG in inhibiting histamine release, and it also had the ability of inhibiting cytokine production by mast cells as steroids do. We concluded that FK506 might regulate allergic diseases via these actions, judging from the viewpoint of clinical relevancy.

FK506肥大细胞和嗜碱性细胞抑制组胺释放和细胞因子产生
肥大细胞和嗜碱性细胞的组胺释放和细胞因子的产生被认为与过敏性疾病的发病密切相关。一些报道表明,FK506(水合他克莫司)抑制肥大细胞和嗜碱性细胞的组胺释放和细胞因子的产生。然而,由于这些报道中并没有将FK506的作用与临床使用的药物进行比较,因此FK506抑制的临床相关性尚不清楚。本文比较了FK506与临床上常用的甾体类药物或甘露糖酸二钠的作用。FK506对褐威大鼠腹膜肥大细胞组胺释放的抑制作用强于类固醇,尤其是DSCG。FK506还能抑制肥大鼠嗜碱性白血病(RBL)-1细胞系和人外周血嗜碱性细胞释放组胺,而类固醇不能抑制人嗜碱性细胞释放组胺。FK506和类固醇抑制RBL-1细胞产生TNF-α和IL-4。因此,FK506在抑制组胺释放方面比类固醇和DSCG更有效,并且与类固醇一样具有抑制肥大细胞产生细胞因子的能力。我们认为,从临床相关性的角度来看,FK506可能通过这些作用调节变态反应性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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