Division of Nephrology, Kanazawa Medical University, Uchinada, Ishikawa, Japan; Renal Section, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Renal Section, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA; Department of Medicine, Boston Medical Center, Boston, Massachusetts, USA.
Kidney Int. 2020 Nov;98(5):1081-1084. doi: 10.1016/j.kint.2020.06.020.
The identification of target antigens in membranous nephropathy has accelerated since the report of M-type phospholipase A2 receptor 1 (PLA2R1). One could say that technological advances have allowed for the demonstration of Moore's law (a doubling every 2 years in the number of transistors that can be fit onto a computer chip) in the field of membranous nephropathy, and that even more antigens can be expected in the near future. In this issue of Kidney International, Sethi et al. describe semaphorin-3B as a novel target antigen, defining a type of membranous nephropathy with onset in the pediatric population.
自 M 型磷脂酶 A2 受体 1(PLA2R1)报道以来,膜性肾病的靶抗原鉴定已经加速。可以说,技术进步使得摩尔定律(计算机芯片上可集成的晶体管数量每两年翻一番)在膜性肾病领域得以实现,并且预计在不久的将来会发现更多的抗原。在本期《国际肾脏病杂志》中,Sethi 等人描述了神经纤毛蛋白-3B 作为一种新的靶抗原,定义了一种在儿科人群中发病的膜性肾病类型。