Elsas P, Lee T H, Lenzi H L, Dessein A J
Ann Inst Pasteur Immunol. 1987 Jan-Feb;138(1):97-116. doi: 10.1016/s0769-2625(87)80099-5.
Recent observations have shown that eosinophils are activated in certain clinical conditions and that activation may enhance the role of eosinophils in immune protection against helminth parasites and in the pathogenesis of certain diseases associated with high eosinophilia. Our laboratory has attempted to identify the immunological mechanisms causing such an activation. The data summarized here show that eosinophils can be activated in vitro with supernatants of resting or stimulated monocytes. The supernatants enhance eosinophil helminthotoxicity by increasing cell degranulation; they also enhance the generation of leukotrienes in eosinophils by exerting a permissive effect on an early step of arachidonic acid metabolism. Biochemical analysis of the enhancing activities suggests that they are carried by a unique molecule or a unique set of molecules whose biochemical and functional properties are different from those of previously described monokines such as IL-1, IFN-alpha,beta, CSF and TNF. Studies on individuals with chronic schistosomiasis suggest that such regulatory interactions between eosinophils and macrophages may take place in the hepatic granulomatous reactions in patients with hepatosplenic schistosomiasis.
最近的观察结果表明,嗜酸性粒细胞在某些临床病症中被激活,而且这种激活可能会增强嗜酸性粒细胞在针对蠕虫寄生虫的免疫保护以及在某些与高嗜酸性粒细胞血症相关疾病的发病机制中的作用。我们实验室试图确定引起这种激活的免疫机制。此处总结的数据表明,嗜酸性粒细胞可被静息或受刺激单核细胞的上清液在体外激活。这些上清液通过增加细胞脱颗粒来增强嗜酸性粒细胞对蠕虫的毒性;它们还通过对花生四烯酸代谢的早期步骤发挥允许作用来增强嗜酸性粒细胞中白三烯的生成。对增强活性的生化分析表明,它们由一种独特的分子或一组独特的分子携带,这些分子的生化和功能特性不同于先前描述的单核因子,如白细胞介素 -1、干扰素 -α、β、集落刺激因子和肿瘤坏死因子。对慢性血吸虫病患者的研究表明,嗜酸性粒细胞与巨噬细胞之间的这种调节相互作用可能发生在肝脾型血吸虫病患者的肝脏肉芽肿反应中。