Nouri-Aria K T, O'Brien F, Noble W, Jabcobson M R, Rajakulasingam K, Durham S R
Upper Respiratory Medicine, National Heart & Lung Institute, and Homerton Hospital, London, UK.
Clin Exp Allergy. 2000 Dec;30(12):1709-16. doi: 10.1046/j.1365-2222.2000.00998.x.
The production of TH2-type cytokines [interleukin-4 (IL-4) and IL-5] and tissue eosinophilia are characteristic features of allergic diseases. It was previously reported that at 24 h after allergen provocation, CD3+ T-lymphocytes were the principal cell source of IL-4 and IL-5 mRNA transcripts in both atopic asthma and rhinitis. To investigate whether IL-4 and IL-5 mRNA are expressed earlier during late nasal responses and if so, which cell(s) are responsible. Nasal biopsies were obtained at 6 h after nasal allergen challenge and following a control challenge with the allergen diluent. Sections were immunostained for T-lymphocytes (CD3+, CD4+) and eosinophils (EG2+). In situ hybridization was used to detect the number of cells expressing messenger RNA (mRNA) for IL-4 and IL-5. In patients with allergic rhinitis, eosinophils (EG2+ cells P = 0. 006) but not T- cells (CD3+ cells) increased in the nasal mucosa at 6 h after allergen challenge. The number of cells expressing IL-4 mRNA (P = 0.01) and IL-5 mRNA (P = 0.05) also increased at 6 h. Co-localization studies showed that 76% of IL-4 mRNA+ cells and 77% of IL-5 mRNA+ cells were eosinophils, whereas at this time point, T-cells and mast cells accounted for </=5% of mRNA expression; the identity of the remaining 20% of IL-4 and IL-5 mRNA+ cells was not determined. By use of immunohistology, cytokine protein expression at 6 h was confirmed for IL-4 but not for IL-5. No increases in T-cells, eosinophils or cytokine expression were detected in non-atopic subjects. Eosinophils represent an early source of IL-4 which may contribute to TH2-type responses during late nasal responses and ongoing allergic rhinitis.
TH2型细胞因子[白细胞介素-4(IL-4)和IL-5]的产生以及组织嗜酸性粒细胞增多是过敏性疾病的特征。先前有报道称,在变应原激发后24小时,CD3 + T淋巴细胞是特应性哮喘和鼻炎中IL-4和IL-5 mRNA转录本的主要细胞来源。为了研究IL-4和IL-5 mRNA在晚期鼻反应中是否更早表达,如果是,哪些细胞对此负责。在鼻变应原激发后6小时以及用变应原稀释液进行对照激发后,获取鼻活检组织。切片进行T淋巴细胞(CD3 +、CD4 +)和嗜酸性粒细胞(EG2 +)免疫染色。原位杂交用于检测表达IL-4和IL-5信使RNA(mRNA)的细胞数量。在变应性鼻炎患者中,变应原激发后6小时鼻黏膜中的嗜酸性粒细胞(EG2 +细胞,P = 0.006)而非T细胞(CD3 +细胞)增加。表达IL-4 mRNA(P = 0.01)和IL-5 mRNA(P = 0.05)的细胞数量在6小时时也增加。共定位研究表明,76%的IL-4 mRNA +细胞和77%的IL-5 mRNA +细胞是嗜酸性粒细胞,而在这个时间点,T细胞和肥大细胞占mRNA表达的≤5%;其余20%的IL-4和IL-5 mRNA +细胞的身份未确定。通过免疫组织学方法,证实了6小时时IL-4的细胞因子蛋白表达,但未证实IL-5的表达。在非特应性受试者中未检测到T细胞、嗜酸性粒细胞或细胞因子表达增加。嗜酸性粒细胞是IL-4的早期来源,可能在晚期鼻反应和持续性变应性鼻炎期间促成TH2型反应。