Berlin Aaron A, Hogaboam Cory M, Lukacs Nicholas W
Department of Pathology, University of Michigan Medical School, 1301 Catherine St., Ann Arbor, 48109-0602, USA.
Lab Invest. 2006 Jun;86(6):557-65. doi: 10.1038/labinvest.3700419.
The progression and severity of chronic asthma likely depends upon the intensity of the damage and remodeling of the tissue. We have developed a chronic model of allergic asthma using multiple cockroach allergen challenges. Using this clinically relevant allergen we have established significant peribronchial fibrosis and mucus overproduction. These remodeling events are accompanied by intense peribronchial inflammation, including lymphocytes and eosinophils. A cytokine that has been identified as having a prominent role in short-term allergic events, stem cell factor (SCF), appears to have a significant role in this late-stage process. Using our polyclonal antibody specific for SCF administered into the airways of mice during the final allergen challenges, we find a significant effect on the chronic peribronchial allergen-induced fibrotic remodeling. This was characterized by reduced inflammation, especially eosinophils, as well as reduced hydroxyproline levels in anti-SCF compared to control antibody-treated animals. In addition, when we examined chemokines associated with the chronic disease and neutralized SCF in vivo we observed a corresponding decrease in CCL6 and CCL17. Using an inhibitor, imatinib mesylate, that blocks SCF/c-kit-associated RTK, we find similar results as with anti-SCF for attenuating AHR and fibrotic changes, suggesting that a potential clinical treatment for chronic asthma already exists related to this pathway. These results further support the potential use of SCF/c-kit inhibition for targeting chronic severe asthmatic responses.
慢性哮喘的进展和严重程度可能取决于组织损伤和重塑的强度。我们利用多次蟑螂过敏原激发建立了一种过敏性哮喘的慢性模型。使用这种与临床相关的过敏原,我们已证实存在显著的支气管周围纤维化和黏液过度产生。这些重塑事件伴随着强烈的支气管周围炎症,包括淋巴细胞和嗜酸性粒细胞。一种在短期过敏事件中被确定起重要作用的细胞因子——干细胞因子(SCF),似乎在这个后期过程中也发挥着重要作用。在最后一次过敏原激发期间,将我们针对SCF的多克隆抗体注入小鼠气道,我们发现其对慢性支气管周围过敏原诱导的纤维化重塑有显著影响。与对照抗体处理的动物相比,这表现为炎症减轻,尤其是嗜酸性粒细胞减少,以及抗SCF组中羟脯氨酸水平降低。此外,当我们检测与该慢性疾病相关的趋化因子并在体内中和SCF时,我们观察到CCL6和CCL17相应减少。使用一种阻断SCF/c-kit相关受体酪氨酸激酶的抑制剂甲磺酸伊马替尼,我们发现其在减轻气道高反应性(AHR)和纤维化改变方面与抗SCF有相似结果,这表明针对该途径的慢性哮喘潜在临床治疗方法已然存在。这些结果进一步支持了SCF/c-kit抑制在针对慢性重度哮喘反应方面的潜在应用。