Department of Medicine, Division of Allergy and Clinical Immunology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Allergy Asthma Immunol Res. 2010 Apr;2(2):87-101. doi: 10.4168/aair.2010.2.2.87. Epub 2010 Mar 24.
Eosinophilia is common feature of many disorders, including allergic diseases. There are many factors that influence the production, migration, survival and death of the eosinophil. Apoptosis is the most common form of physiological cell death and a necessary process to maintain but limit cell numbers in humans and other species. It has been directly demonstrated that eosinophil apoptosis is delayed in allergic inflammatory sites, and that this mechanism contributes to the expansion of eosinophil numbers within tissues. Among the proteins known to influence hematopoiesis and survival, expression of the cytokine interleukin-5 appears to be uniquely important and specific for eosinophils. In contrast, eosinophil death can result from withdrawal of survival factors, but also by activation of pro-apoptotic pathways via death factors. Recent observations suggest a role for cell surface death receptors and mitochondria in facilitating eosinophil apoptosis, although the mechanisms that trigger each of these death pathways remain incompletely delineated. Ultimately, the control of eosinophil apoptosis may someday become another therapeutic strategy for treating allergic diseases and other eosinophil-associated disorders.
嗜酸性粒细胞增多是许多疾病的共同特征,包括过敏疾病。有许多因素影响嗜酸性粒细胞的产生、迁移、存活和死亡。细胞凋亡是细胞生理死亡的最常见形式,是人类和其他物种维持但限制细胞数量所必需的过程。已经直接证明,嗜酸性粒细胞凋亡在过敏炎症部位被延迟,并且该机制有助于组织内嗜酸性粒细胞数量的扩增。在已知影响造血和存活的蛋白质中,细胞因子白细胞介素-5的表达似乎对嗜酸性粒细胞具有独特的重要性和特异性。相比之下,嗜酸性粒细胞的死亡可能是由于生存因子的撤出,也可能是通过死亡因子激活促凋亡途径。最近的观察表明,细胞表面死亡受体和线粒体在促进嗜酸性粒细胞凋亡中起作用,尽管触发这些死亡途径的机制仍不完全明确。最终,控制嗜酸性粒细胞凋亡可能有朝一日成为治疗过敏疾病和其他嗜酸性粒细胞相关疾病的另一种治疗策略。