Blatt Adam Z, Pathan Sabina, Ferreira Viviana P
Department of Medical Microbiology and Immunology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, USA.
Immunol Rev. 2016 Nov;274(1):172-190. doi: 10.1111/imr.12466.
The complement alternative pathway is a powerful arm of the innate immune system that enhances diverse inflammatory responses in the human host. Key to the effects of the alternative pathway is properdin, a serum glycoprotein that can both initiate and positively regulate alternative pathway activity. Properdin is produced by many different leukocyte subsets and circulates as cyclic oligomers of monomeric subunits. While the formation of non-physiological aggregates in purified properdin preparations and the presence of potential properdin inhibitors in serum have complicated studies of its function, properdin has, regardless, emerged as a key player in various inflammatory disease models. Here, we review basic properdin biology, emphasizing the major hurdles that have complicated the interpretation of results from properdin-centered studies. In addition, we elaborate on an emerging role for properdin in thromboinflammation and discuss the potential utility of properdin inhibitors as long-term therapeutic options to treat diseases marked by increased formation of platelet/granulocyte aggregates. Finally, we describe the interplay between properdin and the alternative pathway negative regulator, Factor H, and how aiming to understand these interactions can provide scientists with the most effective ways to manipulate alternative pathway activation in complex systems.
补体替代途径是固有免疫系统的一个强大分支,可增强人类宿主中的多种炎症反应。替代途径发挥作用的关键是备解素,它是一种血清糖蛋白,既能启动替代途径活性,又能对其进行正向调节。备解素由许多不同的白细胞亚群产生,并以单体亚基的环状寡聚体形式循环。尽管纯化的备解素制剂中形成非生理性聚集体以及血清中存在潜在的备解素抑制剂使对其功能的研究变得复杂,但备解素无论如何已成为各种炎症疾病模型中的关键参与者。在此,我们综述备解素的基础生物学,强调那些使以备解素为中心的研究结果解读变得复杂的主要障碍。此外,我们详细阐述备解素在血栓炎症中的新作用,并讨论备解素抑制剂作为长期治疗选择用于治疗以血小板/粒细胞聚集体形成增加为特征的疾病的潜在效用。最后,我们描述备解素与替代途径负调节因子H因子之间的相互作用,以及旨在理解这些相互作用如何能为科学家提供在复杂系统中操纵替代途径激活的最有效方法。