Laberge S, Ernst P, Ghaffar O, Cruikshank W W, Kornfeld H, Center D M, Hamid Q
Meakins-Christie Laboratories and Montreal General Hospital, McGill University, Canada.
Am J Respir Cell Mol Biol. 1997 Aug;17(2):193-202. doi: 10.1165/ajrcmb.17.2.2750.
Asthma is characterized by the presence of activated CD4+ cells in the airways. We hypothesized that the newly characterized cytokine interleukin (IL)-16 is involved in the pathogenesis of asthma through its ability to selectively induce CD4+ cell recruitment within the inflamed bronchial wall. We investigated the expression of IL-16 in bronchial biopsies obtained from subjects with mild asthma (n = 10), atopic nonasthmatic individuals (n = 6), and normal control subjects (n = 10). Cryostat sections from 4% paraformaldehyde-fixed fiberoptic bronchial biopsies were immunostained using a specific antibody that recognizes human IL-16. IL-16 mRNA expression was determined by in situ hybridization. IL-16 immunoreactivity and mRNA were demonstrated mainly in bronchial epithelial cells in all subjects. IL-16 immunoreactivity and IL-16 mRNA expression within the epithelium were significantly higher in bronchial biopsies obtained from asthmatic subjects as compared to both atopic nonasthmatic and normal controls (P < 0.001). The numbers of subepithelial IL-16 immunoreactive cells and IL-16 mRNA-positive cells were also greater in the bronchial biopsies obtained from asthmatic subjects as compared to both atopic nonasthmatic and normal controls (P < 0.001). Epithelial expression of IL-16 immunoreactivity and mRNA correlated with the CD4+ cell infiltration (r2 = 0.70, P < 0.001). There were significant associations between epithelial and subepithelial IL-16 immunoreactivity and airway responsiveness to methacholine. This study demonstates that IL-16 is expressed in airway tissues, particularly in the epithelial cells, and that up-regulation of its expression is a feature of allergic asthma. These results suggest an in vivo role for IL-16 in the pathogenesis of asthma, possibly through the recruitment of CD4+ cells, and support the increasing evidence for the participation of epithelial cells in regulating inflammatory responses.
哮喘的特征是气道中存在活化的CD4+细胞。我们推测新发现的细胞因子白细胞介素(IL)-16通过其在炎症支气管壁内选择性诱导CD4+细胞募集的能力参与哮喘的发病机制。我们研究了从轻度哮喘患者(n = 10)、特应性非哮喘个体(n = 6)和正常对照受试者(n = 10)获取的支气管活检组织中IL-16的表达。使用识别人类IL-16的特异性抗体对4%多聚甲醛固定的纤维支气管活检组织的冰冻切片进行免疫染色。通过原位杂交测定IL-16 mRNA表达。在所有受试者中,IL-16免疫反应性和mRNA主要在支气管上皮细胞中得到证实。与特应性非哮喘和正常对照相比,哮喘患者支气管活检组织上皮内的IL-16免疫反应性和IL-16 mRNA表达显著更高(P < 0.001)。与特应性非哮喘和正常对照相比,哮喘患者支气管活检组织中上皮下IL-16免疫反应性细胞和IL-16 mRNA阳性细胞的数量也更多(P < 0.001)。上皮内IL-16免疫反应性和mRNA的表达与CD4+细胞浸润相关(r2 = 0.70,P < 0.001)。上皮和上皮下IL-16免疫反应性与气道对乙酰甲胆碱的反应性之间存在显著关联。本研究表明IL-16在气道组织中表达,尤其是在上皮细胞中,其表达上调是过敏性哮喘的一个特征。这些结果提示IL-16在哮喘发病机制中可能通过募集CD4+细胞发挥体内作用,并支持上皮细胞参与调节炎症反应的证据不断增加。