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Anti-Fas mAb-induced apoptosis and cytolysis of airway tissue eosinophils aggravates rather than resolves established inflammation

机译:抗Fas mAb诱导的气道组织嗜酸性粒细胞凋亡和细胞溶解加剧而不是解决了既定的炎症

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摘要

BackgroundFas receptor-mediated eosinophil apoptosis is currently forwarded as a mechanism resolving asthma-like inflammation. This view is based on observations in vitro and in airway lumen with unknown translatability to airway tissues in vivo. In fact, apoptotic eosinophils have not been detected in human diseased airway tissues whereas cytolytic eosinophils abound and constitute a major mode of degranulation of these cells. Also, Fas receptor stimulation may bypass the apoptotic pathway and directly evoke cytolysis of non-apoptotic cells. We thus hypothesized that effects of anti-Fas mAb in vivo may include both apoptosis and cytolysis of eosinophils and, hence, that established eosinophilic inflammation may not resolve by this treatment.
机译:背景Fas受体介导的嗜酸性粒细胞凋亡目前作为解决哮喘样炎症的机制而提出。该观点基于体外和在气管腔中对体内气道组织可翻译性未知的观察结果。实际上,在人类患病的气道组织中尚未检测到凋亡性嗜酸性粒细胞,而溶细胞性嗜酸性粒细胞比比皆是,并构成这些细胞脱粒的主要方式。同样,Fas受体刺激可能会绕过凋亡途径,并直接引起非凋亡细胞的细胞溶解。因此,我们推测抗Fas mAb在体内的作用可能包括嗜酸性粒细胞的凋亡和细胞溶解,因此,已建立的嗜酸性粒细胞炎症可能无法通过这种治疗解决。

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