首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Human eosinophils induce histamine release from antigen-activated rat peritoneal mast cells: a possible role for mast cells in late-phase allergic reactions.
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Human eosinophils induce histamine release from antigen-activated rat peritoneal mast cells: a possible role for mast cells in late-phase allergic reactions.

机译:人类嗜酸性粒细胞诱导抗原活化的大鼠腹膜肥大细胞释放组胺:肥大细胞在后期变态反应中的可能作用。

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摘要

BACKGROUND: Mast cells and eosinophils are believed to interact during the late and the chronic stages of allergic inflammation. OBJECTIVE: In this study we investigated whether eosinophils can cause activation and consequent histamine release of already challenged mast cells, a situation likely to take place during the allergic late-phase reaction. METHODS: Rat peritoneal mast cells presensitized with IgE anti-dinitrophenol-human serum albumin and challenged by dinitrophenol-human serum albumin or compound 48/80 were incubated with either eosinophil sonicate or major basic protein (MBP). Eosinophils were purified from the peripheral (>98%) blood of mildly allergic patients. Heparin and pertussis toxin and different extracellular Ca(2+) concentrations were used to modulate mast cell reactivation by MBP. Histamine release was assessed as a marker of mast cell activation. RESULTS: IgE-challenged mast cells were sensitive to reactivation induced by eosinophil sonicate and MBP. Reactivation was not cytotoxic for the mast cells. Mast cells previously challenged with compound 48/80 did not respond to subsequent MBP activation. Furthermore, heparin and pertussis toxin both inhibited mast cell reactivation induced by MBP. The ability of eosinophil sonicate and MBP to activate mast cells was not significantly affected at the different Ca(2+) concentrations. CONCLUSIONS: In summary, we have shown a direct activating activity of eosinophils, partially due to MBP, toward IgE-challenged and immunologically desensitized mast cells. This suggests that in vivo mast cells can be reactivated during a late-phase reaction to release histamine by a non-IgE-dependent mechanism.
机译:背景:肥大细胞和嗜酸性粒细胞被认为在变态性炎症的晚期和慢性阶段相互作用。目的:在这项研究中,我们研究了嗜酸性粒细胞是否会引起已经激发的肥大细胞的活化和随后的组胺释放,这种情况很可能发生在变态反应后期。方法:将预免疫IgE抗二硝基苯酚-人血清白蛋白并经二硝基苯酚-人血清白蛋白或化合物48/80攻击的大鼠腹膜肥大细胞与嗜酸性粒细胞超声或主要碱性蛋白(MBP)孵育。从轻度过敏患者的外周血(> 98%)中纯化嗜酸性粒细胞。肝素和百日咳毒素和不同的细胞外Ca(2+)浓度用于调节MBP肥大细胞的激活。组胺释放被评估为肥大细胞活化的标志。结果:IgE挑战的肥大细胞对嗜酸性粒细胞超声和MBP诱导的再激活敏感。复活对于肥大细胞没有细胞毒性。先前用化合物48/80攻击的肥大细胞不响应随后的MBP激活。此外,肝素和百日咳毒素均抑制MBP诱导的肥大细胞再激活。嗜酸性粒细胞超声和MBP激活肥大细胞的能力在不同的Ca(2+)浓度下未受到明显影响。结论:总的来说,我们已经表明,嗜酸性粒细胞对IgE挑战和免疫脱敏的肥大细胞具有直接激活活性,部分是由于MBP所致。这表明可以通过非IgE依赖性机制在后期反应期间使体内肥大细胞再活化以释放组胺。

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