O'Sullivan Siobhán M
Royal Irish Academy, 19 Dawson St, Dublin 2 Ireland.
Proc Am Thorac Soc. 2005;2(2):162-5. doi: 10.1513/pats.200502-016AW.
Despite advances in the understanding of the pathophysiology of asthma and the availability of effective treatment, the World Health Organization estimates that asthma accounts for 1 in every 250 deaths worldwide. Viruses are associated with half of all asthma exacerbations. The immune response to viral infection may enhance preexisting airway inflammation via the release of chemokines and cytokines and local recruitment of inflammatory cells. Murine models have provided evidence for a deleterious role for CD8+ T cells in the context of respiratory viral infection. Passive transfer of respiratory syncytial virus-specific cytotoxic T lymphocytes (CTLs) to infected mice results in virus clearance, which is associated with acute and sometimes fatal pulmonary disease. Compared with control subjects, CD8+ cells appear to be preferentially sequestered in the airways of individuals with asthma during acute exacerbations. In addition, an expanded CD8+ T cell population, dominated by activated cytotoxic CD8+ lymphocytes, has been documented in biopsies from patients dying as a result of acute asthma in association with a viral infection. Undoubtedly, CD8+ CTLs are a crucial in cell-mediated immunity in response to respiratory viruses. However, it would appear that an aberrant CD8+ T cell response in the context of a viral infection may place individuals with asthma at risk for fatal asthma.
尽管在哮喘病理生理学的理解以及有效治疗方法的可得性方面取得了进展,但世界卫生组织估计,哮喘在全球每250例死亡中占1例。病毒与所有哮喘加重病例中的一半相关。对病毒感染的免疫反应可能通过趋化因子和细胞因子的释放以及炎症细胞的局部募集来增强先前存在的气道炎症。小鼠模型已为CD8 + T细胞在呼吸道病毒感染情况下的有害作用提供了证据。将呼吸道合胞病毒特异性细胞毒性T淋巴细胞(CTL)被动转移到感染的小鼠中会导致病毒清除,这与急性且有时致命的肺部疾病有关。与对照受试者相比,在急性加重期间,CD8 +细胞似乎优先隔离在哮喘患者的气道中。此外,在因急性哮喘合并病毒感染而死亡的患者活检中,已记录到以活化的细胞毒性CD8 +淋巴细胞为主的CD8 + T细胞群体扩大。毫无疑问,CD8 + CTL在针对呼吸道病毒的细胞介导免疫中至关重要。然而,在病毒感染的情况下,异常的CD8 + T细胞反应似乎可能使哮喘患者面临致命哮喘的风险。