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Respiratory viral infections and asthma pathogenesis: A critical role for dendritic cells?

机译:呼吸道病毒感染和哮喘发病机制:树突状细胞的关键作用?

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BACKGROUND:: Respiratory viral infections can influence the course of asthma at different time points. Severe respiratory viral infections during early age are associated with a higher prevalence of asthma in later childhood. In established asthma, viral infections are a frequent cause of asthma exacerbation. OBJECTIVES:: The present review focuses on epidemiological and experimental animal data that can illuminate the mechanisms by which viral infections can lead to sensitization to antigen, and exacerbate ongoing allergic airway inflammation and focuses on the role played by dendritic cells (DCs). RESULTS:: In experimental rodent models of asthma, respiratory viral infection at the time of a first inhaled antigen exposure is described to induce Th2 sensitization and to enhance the allergic response to a second encounter with the same antigen. Virus infections can modulate airway dendritic cell function by upregulation of costimulatory molecule expression, enhanced recruitment, and by inducing an inflammatory environment, all leading to an enhanced antigen presentation and possibly changing the normal tolerogenic response to inhaled antigen into an immunogenic response. In established asthma, respiratory viral infections attract several inflammatory cells, alter receptor expression on airway smooth muscle and modulate neuroimmune mechanisms, possibly leading to exacerbation of disease. CONCLUSIONS:: Animal data suggest that the link between respiratory viral infections and increased asthma is causally related, the viral infection acting on the immune and structural cells to enhance antigen presentation and inflammatory cell recruitment.
机译:背景:呼吸道病毒感染可在不同时间点影响哮喘病程。幼儿时期严重的呼吸道病毒感染与儿童后期哮喘的患病率较高有关。在已建立的哮喘中,病毒感染是哮喘恶化的常见原因。目的:本综述重点关注流行病学和实验动物数据,这些数据可以阐明病毒感染可导致对抗原致敏的机制,并加剧正在进行的过敏性气道炎症,并着重研究树突状细胞(DC)的作用。结果:在哮喘实验性啮齿动物模型中,首次吸入抗原暴露时呼吸道病毒感染被描述为诱导Th2致敏并增强对第二次接触相同抗原的过敏反应。病毒感染可通过上调共刺激分子表达,增强募集和诱导炎症环境来调节气道树突细胞功能,所有这些都会导致抗原呈递增加,并可能将对吸入抗原的正常致耐受性反应转变为免疫原性反应。在已建立的哮喘中,呼吸道病毒感染会吸引多个炎症细胞,改变气道平滑肌上的受体表达并调节神经免疫机制,可能导致疾病加重。结论:动物数据表明,呼吸道病毒感染与哮喘的增加之间存在因果关系,病毒感染作用于免疫细胞和结构细胞,从而增强抗原呈递和炎症细胞募集。

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