Rosenberg Helene F, Phipps Simon, Foster Paul S
Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
J Allergy Clin Immunol. 2007 Jun;119(6):1303-10; quiz 1311-2. doi: 10.1016/j.jaci.2007.03.048. Epub 2007 May 3.
Blood eosinophilia and tissue eosinophilia are characteristic features of allergic inflammation and asthma, conditions associated with prominent production of T(H)2 cytokines IL-4, IL-5, and IL-13. In this review, we will consider recent advances in our understanding of the molecular mechanisms that promote expansion and differentiation of eosinophil progenitors in bone marrow, eosinophil recruitment in response to chemokine receptor 3 agonists eosinophil transit mediated by specific ligand-receptor interactions, and prolonged survival of eosinophils in peripheral tissues. Novel rational therapies including antiselectin and antichemokine receptor modalities designed to block eosinophil development and trafficking are discussed, together with the implications of recent clinical studies that have evaluated the efficacy of humanized anti-IL-5 mAb therapy.
血液嗜酸性粒细胞增多和组织嗜酸性粒细胞增多是变应性炎症和哮喘的特征性表现,这些病症与T(H)2细胞因子IL-4、IL-5和IL-13的大量产生有关。在本综述中,我们将探讨在促进骨髓中嗜酸性粒细胞祖细胞扩增和分化、趋化因子受体3激动剂介导的嗜酸性粒细胞募集、特定配体-受体相互作用介导的嗜酸性粒细胞转运以及外周组织中嗜酸性粒细胞的长期存活等分子机制方面的最新进展。我们还将讨论旨在阻断嗜酸性粒细胞发育和转运的新型合理疗法,包括抗选择素和抗趋化因子受体疗法,以及评估人源化抗IL-5单克隆抗体疗法疗效的近期临床研究的意义。