Fonseca-Aten Monica, Okada Pamela J, Bowlware Karen L, Chavez-Bueno Susana, Mejias Asuncion, Rios Ana Maria, Katz Kathy, Olsen Kurt, Ng Simon, Jafri Hasan S, McCracken George H, Ramilo Octavio, Hardy R Doug
Departments of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9063, USA.
Ann Allergy Asthma Immunol. 2006 Oct;97(4):457-63. doi: 10.1016/S1081-1206(10)60935-0.
Clarithromycin is postulated to possess immunomodulatory properties in addition to its antimicrobial activity.
To evaluate the effect of clarithromycin on serum and nasopharyngeal cytokine and chemokine concentrations in children with an acute exacerbation of recurrent wheezing.
Children with a history of recurrent wheezing or asthma and who presented with an acute exacerbation of wheezing were enrolled in a double-blind, randomized trial of clarithromycin vs placebo. Concentrations of tumor necrosis factor alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-1beta (IL-1beta), IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, granulocyte-macrophage colony-stimulating factor, RANTES, eotaxin, macrophage inflammatory protein 1alpha, macrophage inflammatory protein 1beta, and monocyte chemoattractant protein 1 were measured in serum and/or nasopharyngeal aspirates before, during, and after therapy. Mycoplasma pneumoniae and Chlamydophila pneumoniae infection were evaluated for by polymerase chain reaction and serologic testing.
Nasopharyngeal concentrations of TNF-alpha, IL-1beta, and IL-10 were significantly and persistently lower in children treated with clarithromycin compared with placebo. There tended to be a greater effect of clarithromycin on nasopharyngeal cytokine concentrations in patients with evidence of M. pneumoniae or C. pneumoniae infection. No significant differences were detected in serum cytokines for children treated with clarithromycin compared with placebo.
Clarithromycin therapy reduces mucosal TNF-alpha, IL-1beta, and IL-10 concentrations in children with an acute exacerbation of recurrent wheezing.
除抗菌活性外,克拉霉素还被认为具有免疫调节特性。
评估克拉霉素对反复喘息急性加重期儿童血清及鼻咽部细胞因子和趋化因子浓度的影响。
有反复喘息或哮喘病史且出现喘息急性加重的儿童被纳入一项克拉霉素与安慰剂对照的双盲随机试验。在治疗前、治疗期间和治疗后,检测血清和/或鼻咽抽吸物中肿瘤坏死因子α(TNF-α)、干扰素-γ(IFN-γ)、白细胞介素-1β(IL-1β)、IL-2、IL-4、IL-5、IL-6、IL-8、IL-10、粒细胞-巨噬细胞集落刺激因子、调节激活正常T细胞表达和分泌因子(RANTES)、嗜酸性粒细胞趋化因子、巨噬细胞炎性蛋白1α、巨噬细胞炎性蛋白1β和单核细胞趋化蛋白1的浓度。通过聚合酶链反应和血清学检测评估肺炎支原体和肺炎衣原体感染情况。
与安慰剂相比,接受克拉霉素治疗的儿童鼻咽部TNF-α、IL-1β和IL-10浓度显著且持续降低。在有肺炎支原体或肺炎衣原体感染证据的患者中,克拉霉素对鼻咽部细胞因子浓度的影响似乎更大。与安慰剂相比,接受克拉霉素治疗的儿童血清细胞因子未检测到显著差异。
克拉霉素治疗可降低反复喘息急性加重期儿童黏膜TNF-α、IL-1β和IL-10的浓度。