Bandeira-Melo C, Bozza P T, Diaz B L, Cordeiro R S, Jose P J, Martins M A, Serhan C N
Department of Physiology and Pharmacodynamics, Oswaldo Cruz Institute, Fundaçao Oswaldo Cruz, Rio de Janeiro, Brazil.
J Immunol. 2000 Mar 1;164(5):2267-71. doi: 10.4049/jimmunol.164.5.2267.
Tissue eosinophilia prevention represents one of the primary targets to new anti-allergic therapies. As lipoxin A4 (LXA4) and aspirin-triggered 15-epi-LXA4 (ATL) are emerging as endogenous "stop signals" produced in distinct pathologies including some eosinophil-related pulmonary disorders, we evaluated the impact of in situ LXA4/ATL metabolically stable analogues on allergen-induced eosinophilic pleurisy in sensitized rats. LXA4/ATL analogues dramatically blocked allergic pleural eosinophil influx, while concurrently increasing circulating eosinophilia, inhibiting the earlier edema and neutrophilia associated with allergic reaction. The mechanisms underlying this LXA4/ATL-driven allergic eosinophilia blockade was independent of mast cell degranulation and involved LXA4/ATL inhibition of both IL-5 and eotaxin generation, as well as platelet activating factor action. These findings reveal LXA4/ATL as a novel class of endogenous anti-allergic mediators, capable of preventing local eosinophilia.
组织嗜酸性粒细胞增多的预防是新型抗过敏疗法的主要目标之一。由于脂氧素A4(LXA4)和阿司匹林触发的15-表-LXA4(ATL)作为内源性“终止信号”出现在包括一些嗜酸性粒细胞相关肺部疾病在内的不同病理过程中,我们评估了原位LXA4/ATL代谢稳定类似物对致敏大鼠变应原诱导的嗜酸性粒细胞性胸膜炎的影响。LXA4/ATL类似物显著阻断了过敏性胸膜嗜酸性粒细胞浸润,同时增加了循环嗜酸性粒细胞增多,抑制了与过敏反应相关的早期水肿和中性粒细胞增多。这种由LXA4/ATL驱动的过敏性嗜酸性粒细胞增多阻断的机制独立于肥大细胞脱颗粒,涉及LXA4/ATL对IL-5和嗜酸性粒细胞趋化因子生成以及血小板活化因子作用的抑制。这些发现揭示LXA4/ATL是一类新型的内源性抗过敏介质,能够预防局部嗜酸性粒细胞增多。