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白细胞介素-8和调节激活正常T细胞表达和分泌的因子可抑制由单核细胞趋化和激活因子/单核细胞趋化蛋白-1以及组胺释放因子诱导的嗜碱性粒细胞组胺释放。

Interleukin-8 and RANTES inhibit basophil histamine release induced with monocyte chemotactic and activating factor/monocyte chemoattractant peptide-1 and histamine releasing factor.

作者信息

Alam R, Forsythe P A, Lett-Brown M A, Grant J A

机构信息

Department of Medicine, University of Texas Medical Branch, Galveston 77550.

出版信息

Am J Respir Cell Mol Biol. 1992 Oct;7(4):427-33. doi: 10.1165/ajrcmb/7.4.427.

DOI:10.1165/ajrcmb/7.4.427
PMID:1382479
Abstract

The objective of this study was to investigate the effect of interleukin-8 (IL-8) and RANTES on basophil histamine release induced with monocyte chemoattractant peptide-1 (MCP-1) and crude histamine releasing factor (HRF). IL-8 induced low levels of histamine release (8.5 +/- 0.5%) from basophils obtained from only six of 20 donors at high concentrations (10(-6) M). RANTES induced histamine release (16 +/- 2%) from basophils of four of 15 donors at 10(-7) M concentration. However, both IL-8 and RANTES inhibited MCP-1 and HRF-induced histamine release from basophils dose-dependently at concentrations of 10(-9) to 10(-7) M. Basophils from all donors showed a significant inhibitory response (greater than 15%). The maximal inhibition of MCP-1 and HRF by IL-8 was 28 +/- 4% and 48 +/- 8%, respectively. The maximal inhibition of MCP-1 and HRF by RANTES was 26 +/- 4% and 43 +/- 6%, respectively. Peripheral blood mononuclear cell-derived HRF was purified into three distinct peaks by reverse-phase high performance liquid chromatography. Peak I contained MCP-1 as judged by binding to an immunoaffinity column that was prepared with anti-MCP-1 antibody. IL-8 inhibited histamine release induced with all three peaks of HRF. The inhibition of histamine release by IL-8 was significantly higher in normal subjects than in allergic patients (59 +/- 9% versus 31 +/- 7%, P less than 0.05). Both IL-8 and RANTES inhibited cytokine-induced histamine release only and did not affect histamine release by anti-IgE, FMLP, and C5a.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是探讨白细胞介素-8(IL-8)和调节激活正常T细胞表达和分泌的趋化因子(RANTES)对单核细胞趋化蛋白-1(MCP-1)和粗制组胺释放因子(HRF)诱导的嗜碱性粒细胞组胺释放的影响。IL-8在高浓度(10⁻⁶ M)时仅能诱导20名供体中6名供体的嗜碱性粒细胞释放低水平的组胺(8.5±0.5%)。RANTES在10⁻⁷ M浓度时能诱导15名供体中4名供体的嗜碱性粒细胞释放组胺(16±2%)。然而,在10⁻⁹至10⁻⁷ M浓度下,IL-8和RANTES均能剂量依赖性地抑制MCP-1和HRF诱导的嗜碱性粒细胞组胺释放。所有供体的嗜碱性粒细胞均表现出显著的抑制反应(大于15%)。IL-8对MCP-1和HRF的最大抑制率分别为28±4%和48±8%。RANTES对MCP-1和HRF的最大抑制率分别为26±4%和43±6%。外周血单个核细胞来源的HRF通过反相高效液相色谱法纯化出三个不同的峰。通过与用抗MCP-1抗体制备的免疫亲和柱结合判断,峰I含有MCP-1。IL-8抑制由HRF的所有三个峰诱导的组胺释放。IL-8对组胺释放的抑制在正常受试者中显著高于过敏患者(59±9%对31±7%,P<0.05)。IL-8和RANTES均仅抑制细胞因子诱导的组胺释放,而不影响抗IgE、FMLP和C5a诱导的组胺释放。(摘要截短于250字)

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