Molecular Pathology Research Group, Institute of Medical Biology, Faculty of Health Science, University of Tromsø, N-9037 Tromsø, Norway.
Arthritis Res Ther. 2011 Apr 18;13(2):214. doi: 10.1186/ar3281.
The present review focuses on pathogenic molecular and transcriptional events in patients with lupus nephritis. These factors are renal DNaseI, exposed chromatin fragments and the corresponding chromatin-reactive autoantibodies. Lupus nephritis is the most serious complication in human systemic lupus erythematosus, and is characterised by deposition of chromatin fragment-IgG complexes in the mesangial matrix and glomerular basement membranes. The latter deposition defines end-stage disease. This event is stringently linked to a renal-restricted shutdown of expression of the DNaseI gene, as determined by loss of DNaseI mRNA level and DNaseI enzyme activity. The major aim of the present review is to generate new therapeutic strategies based on new insight into the disease pathogenesis.
本文综述了狼疮肾炎患者中致病的分子和转录事件。这些因素包括肾脱氧核糖核酸酶 I、暴露的染色质片段和相应的染色质反应性自身抗体。狼疮肾炎是人类系统性红斑狼疮中最严重的并发症,其特征是染色质片段-IgG 复合物在系膜基质和肾小球基底膜中的沉积。后者的沉积定义了终末期疾病。这一事件与肾特异性的脱氧核糖核酸酶 I 基因表达关闭严格相关,这可通过脱氧核糖核酸酶 I mRNA 水平和脱氧核糖核酸酶 I 酶活性的丧失来确定。本文的主要目的是基于对疾病发病机制的新认识,提出新的治疗策略。