Haczku A
Department of Pediatrics, National Jewish Medical and Research Center, Denver, USA.
Acta Microbiol Immunol Hung. 1998;45(1):19-29.
The bronchial inflammation characterising asthma represents a specialised form of cell-mediated immune reactions, in which products of activated CD4+ T cells orchestrate the accumulation and activation of granulocytes, particularly eosinophils. Through their toxic granule proteins, membrane derived lipid mediators and proinflammatory cytokines, eosinophils are suggested to be responsible for the changes in airway submucosal tissue resulting in altered airway responsiveness. T cell activation is followed by the synthesis and release of cytokines of which IL-3, IL-5 and GM-CSF are particularly important in the site-specific accumulation, prolonged survival and activation of eosinophils. This review focuses on the interaction of these two cell types with particular interest in the cytokines which may be responsible for the development of eosinophilic airway inflammation.
哮喘所特有的支气管炎症代表了一种细胞介导的免疫反应的特殊形式,其中活化的CD4+ T细胞产物协调粒细胞尤其是嗜酸性粒细胞的聚集和活化。通过其毒性颗粒蛋白、膜衍生脂质介质和促炎细胞因子,嗜酸性粒细胞被认为是导致气道黏膜下组织变化从而引起气道反应性改变的原因。T细胞活化后会合成并释放细胞因子,其中IL-3、IL-5和GM-CSF在嗜酸性粒细胞的位点特异性聚集、延长存活时间和活化方面尤为重要。本综述重点关注这两种细胞类型的相互作用,特别关注可能导致嗜酸性气道炎症发展的细胞因子。