Liu Yujuan, Anders Hans-Joachim
Nephrologisches Zentrum, Medizinische Klinik und Poliklinik IV, Klinikum der Universität, München, Munich, Germany.
Nephron Clin Pract. 2014;128(3-4):224-31. doi: 10.1159/000368581. Epub 2014 Nov 8.
BACKGROUND/AIMS: Lupus nephritis is an organ manifestation of systemic autoimmunity. Current treatment algorithms are still based on unselective immunosuppressive drugs. There is hope that highly selective biological drugs could be as or even more effective but less toxic. A profound understanding of the pathogenesis of lupus nephritis is necessary to identify the optimal molecular targets.
PubMed and www.clincialtrials.gov were searched using 'lupus nephritis' as the key word.
The pathogenesis of lupus nephritis is based (1) on the mechanisms that lead to loss of tolerance against nuclear autoantigens, i.e. systemic lupus, and then (2) on the mechanisms of immune complex-induced intrarenal inflammation. Systemic lupus develops when genetic variants allow autoimmunization against nuclear autoantigens, e.g. by impairing lymphocyte depletion via apoptosis, opsonization, and rapid phagocytic clearance. This allows endogenous nucleic acids to directly activate Toll-like receptors on dendritic cells or B cells, a process that drives IFN-α-driven immunity, antigen presentation, and the activation of autoreactive lymphocyte subsets. Activation of B cells and their maturation to plasma cells promotes autoantibody production and subsequent immune complex glomerulonephritis. Complement and numerous proinflammatory cytokines drive the inflammatory process that can cause kidney injury, scarring, and chronic kidney disease.
Systemic lupus is more a variable syndrome than a single disorder based on heterogeneous genetic variants and complex aberrant immune alterations. This makes it less likely that a single specific biological drug will be as efficient as currently used unselective immunosuppressive drugs. Autoantibody production and intrarenal immune complex formation are the hallmark of lupus nephritis. However, kidney injury and scarring also result from local amplification of tissue inflammation. Therefore, a combination of unselective immunosuppressive and biological drugs that block immune cell recruitment or proinflammatory cytokines may be promising to improve disease outcomes in lupus nephritis.
背景/目的:狼疮性肾炎是系统性自身免疫的一种器官表现。目前的治疗方案仍基于非选择性免疫抑制药物。人们希望高选择性生物药物可能同样有效甚至更有效,但毒性更低。深入了解狼疮性肾炎的发病机制对于确定最佳分子靶点至关重要。
以“狼疮性肾炎”为关键词检索PubMed和www.clincialtrials.gov。
狼疮性肾炎的发病机制基于:(1)导致对核自身抗原耐受性丧失的机制,即系统性红斑狼疮,然后(2)基于免疫复合物诱导的肾内炎症机制。当基因变异允许针对核自身抗原进行自身免疫时,例如通过损害淋巴细胞经凋亡、调理作用和快速吞噬清除的耗竭,系统性红斑狼疮就会发生。这使得内源性核酸能够直接激活树突状细胞或B细胞上的Toll样受体,这一过程驱动干扰素-α驱动的免疫、抗原呈递以及自身反应性淋巴细胞亚群的激活。B细胞的激活及其向浆细胞的成熟促进自身抗体的产生以及随后的免疫复合物性肾小球肾炎。补体和众多促炎细胞因子驱动可导致肾损伤、瘢痕形成和慢性肾脏病的炎症过程。
系统性红斑狼疮更像是一种可变综合征,而非基于异质基因变异和复杂异常免疫改变的单一疾病。这使得单一特定生物药物不太可能像目前使用的非选择性免疫抑制药物那样有效。自身抗体产生和肾内免疫复合物形成是狼疮性肾炎的标志。然而,肾损伤和瘢痕形成也源于组织炎症的局部放大。因此,非选择性免疫抑制药物与阻断免疫细胞募集或促炎细胞因子的生物药物联合使用可能有望改善狼疮性肾炎的疾病结局。