Immunology Research Group, Department of Microbiology and Infectious Diseases, University of Calgary, 4A31 HRIC, 3330 Hospital Dr. NW, Calgary, AB, Canada.
Arch Immunol Ther Exp (Warsz). 2010 Aug;58(4):273-7. doi: 10.1007/s00005-010-0082-1. Epub 2010 May 26.
Uric acid crystals, the causative agent of gout, have recently gained widespread attention due to their role as a natural endogenous adjuvant. Uric acid crystals, first sensed extracellularly by membrane lipid alterations, are internalized and subsequently activate the NLRP3 inflammasome. Currently, various aspects of this particular novel pathway are poorly defined. This short review will focus on some recent discoveries regarding this simple crystalline structure and address areas requiring further investigation. The fact that uric acid crystals activate innate host defense mechanisms, triggering robust inflammation and immune activation, may lead to engineering potent adjuvants for future vaccines. Furthermore, the elucidation of uric acid's mechanism of inflammation may lay the foundation for other solid inflammatory structures such as silica, asbestos, and alum.
尿酸晶体作为一种天然的内源性佐剂,其作用最近受到了广泛关注。尿酸晶体首先通过细胞膜脂质改变在细胞外被感知,然后被内化,并随后激活 NLRP3 炎性体。目前,这一特殊新途径的各个方面还没有得到很好的定义。这篇简短的综述将集中讨论一些关于这种简单晶体结构的最新发现,并探讨需要进一步研究的领域。尿酸晶体激活先天宿主防御机制,引发强烈的炎症和免疫激活这一事实,可能为未来的疫苗工程提供有效的佐剂。此外,阐明尿酸的炎症机制可能为其他固体炎症结构(如二氧化硅、石棉和明矾)奠定基础。