Iliopoulos O, Baroody F M, Naclerio R M, Bochner B S, Kagey-Sobotka A, Lichtenstein L M
Johns Hopkins University School of Medicine, Department of Medicine (Division of Clinical Immunology), Baltimore, MD 21224.
J Immunol. 1992 Apr 1;148(7):2223-8.
The pattern of mediators and appearance of cells that stain with alcian blue during human experimental early and late phase allergic reactions suggest that basophils accumulate in nasal secretions within hours of local Ag stimulation. To further explore whether the histamine containing cells that enter the nose after Ag challenge are mast cells or basophils, we studied their functional and phenotypic characteristics. Approximately 24 h after intranasal Ag provocation of subjects with allergic rhinitis, nasal lavage was performed, and the cells were isolated for degranulation studies, analysis of surface Ag, and viability. The average histamine content per alcian blue staining cell was 0.78 +/- 0.2 pg (n = 7), similar to that reported for peripheral blood basophils. Nasal cells were challenged in vitro with anti-IgE, ragweed Amb a I, and FMLP and their responses were compared to those of peripheral blood basophils isolated simultaneously from the same donors. Nasal leukocytes released histamine maximally at 0.1 micrograms/ml of anti-IgE (35.8 +/- 7.8%, n = 7) and responded to FMLP (25.4 +/- 9.9%, n = 7). The response of the cells to ragweed Amb a I and anti-IgE was attenuated compared to peripheral blood basophils. Anti-IgE-induced histamine release was calcium and temperature dependent. Dual color immunofluorescence and flow cytometric analysis of the recovered nasal cells coexpressed CD18, a leukocyte marker not expressed by mast cells. The nasal cells consistently had high levels of spontaneous histamine release (19.5 +/- 2.0%, n = 22). The viability of all cells, assessed by erythrosin B dye exclusion, was 70 +/- 2% (n = 15). However, the viability of IgE-bearing cells was only 28.3 +/- 5.7% (n = 4). The characteristics of histamine release and the nature of the cellular surface markers provide functional proof that the histamine-containing cells accumulating after nasal Ag challenge are basophils and not mast cells.
在人类实验性早期和晚期过敏反应中,与阿尔辛蓝染色的介质模式和细胞外观表明,在局部抗原刺激数小时内,嗜碱性粒细胞在鼻分泌物中积聚。为了进一步探究抗原激发后进入鼻腔的含组胺细胞是肥大细胞还是嗜碱性粒细胞,我们研究了它们的功能和表型特征。在对变应性鼻炎患者进行鼻内抗原激发后约24小时,进行鼻腔灌洗,并分离细胞进行脱颗粒研究、表面抗原分析和活力检测。每个阿尔辛蓝染色细胞的平均组胺含量为0.78±0.2皮克(n = 7),与外周血嗜碱性粒细胞的报道相似。用抗IgE、豚草Amb a I和FMLP在体外刺激鼻腔细胞,并将它们的反应与同时从相同供体分离的外周血嗜碱性粒细胞的反应进行比较。鼻腔白细胞在0.1微克/毫升抗IgE时组胺释放最大(35.8±7.8%,n = 7),并对FMLP有反应(25.4±9.9%,n = 7)。与外周血嗜碱性粒细胞相比,细胞对豚草Amb a I和抗IgE的反应减弱。抗IgE诱导的组胺释放依赖于钙和温度。对回收的鼻腔细胞进行双色免疫荧光和流式细胞术分析,共表达CD18,这是一种肥大细胞不表达的白细胞标志物。鼻腔细胞始终具有高水平的自发组胺释放(19.5±2.0%,n = 22)。通过赤藓红B染料排除法评估的所有细胞活力为70±2%(n = 15)。然而,含IgE细胞的活力仅为28.3±5.7%(n = 4)。组胺释放的特征和细胞表面标志物的性质提供了功能证据,表明鼻内抗原激发后积聚的含组胺细胞是嗜碱性粒细胞而非肥大细胞。