Matković Svjetlana, Vojvodić Danilo, Baljosevic Ivan
ORL Clinic, Military Medical Academy, Belgrade, Serbia.
Eur Arch Otorhinolaryngol. 2007 Nov;264(11):1283-7. doi: 10.1007/s00405-007-0373-2. Epub 2007 Jul 21.
Chronic secretory otitis relates to the permanent presence of secretion in the middle ear for more than 3 months. The reason why applied therapy is often ineffective is that, for now, etiopathogenic molecular mechanisms responsible for the cause and the course of the secretory process in the mucus of the middle ear have not been precisely defined. Cytokines are the key mediators in middle ear inflammation with secretory otitis and regulating different inflammation states can add to the cause of the molecular processes that lead to hystopathological changes in mucus and submucus characteristically for the chronic state of secretory otitis. The aim of our work was to define the pro-inflammatory, immunoregulatory and allergy-associated cytokine levels in middle ear secretion samples of diseased children and to compare the defined values with the secretory process continuance in groups of patients who were diseased for more or less than 3 months. According to the results that have showed higher concentration of all ten examined cytokines in the secretion samples of the children who had secretory otitis for a longer time, it can be concluded that the disturbance expression regulation of the pro-inflammatory TNFalpha, TNFbeta, IL1beta, IFNgamma, IL-6 and IL-8, as well as immunoregulatory IL-2 and IL-10, and allergy associated cytokines IL-4 and IL-5 relating to the hyper production can add to the conversion of the inflammatory process to the chronic state, which has been maintained for longer than 3 months.
慢性分泌性中耳炎是指中耳分泌物持续存在超过3个月。目前应用的治疗方法往往无效,原因在于,导致中耳黏液分泌过程的病因及病程的致病分子机制尚未明确界定。细胞因子是分泌性中耳炎中耳炎症的关键介质,调节不同的炎症状态可能会引发分子过程,导致黏液和黏膜下层出现符合慢性分泌性中耳炎特征的组织病理学变化。我们研究的目的是确定患病儿童中耳分泌物样本中促炎、免疫调节和过敏相关细胞因子的水平,并将确定的值与患病3个月以上或以下的患者组中分泌过程的持续时间进行比较。根据结果显示,患有分泌性中耳炎时间较长的儿童的分泌物样本中,所有十种检测的细胞因子浓度都较高,可以得出结论,促炎细胞因子TNFα、TNFβ、IL1β、IFNγ、IL-6和IL-8,以及免疫调节细胞因子IL-2和IL-10,和过敏相关细胞因子IL-4和IL-5的表达调节紊乱与过量产生,可能会促使炎症过程转变为持续超过3个月的慢性状态。