Podolska Malgorzata J, Biermann Mona Hc, Maueröder Christian, Hahn Jonas, Herrmann Martin
Department of Internal Medicine 3, Institute for Clinical Immunology and Rheumatology, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany.
J Inflamm Res. 2015 Aug 20;8:161-71. doi: 10.2147/JIR.S70325. eCollection 2015.
The immune system struggles every day between responding to foreign antigens and tolerating self-antigens to delicately maintain tissue homeostasis. If self-tolerance is broken, the development of autoimmunity can be the consequence, as it is in the case of the chronic inflammatory autoimmune disease systemic lupus erythematosus (SLE). SLE is considered to be a multifactorial disease comprising various processes and cell types that act abnormally and in a harmful way. Oxidative stress, infections, or, in general, tissue injury are accompanied by massive cellular demise. Several processes such as apoptosis, necrosis, or NETosis (formation of Neutrophil Extracellular Traps [NETs]) may occur alone or in combination. If clearance of dead cells is insufficient, cellular debris may accumulate and trigger inflammation and leakage of cytoplasmic and nuclear autoantigens like ribonucleoproteins, DNA, or histones. Inadequate removal of cellular remnants in the germinal centers of secondary lymphoid organs may result in the presentation of autoantigens by follicular dendritic cells to autoreactive B cells that had been generated by chance during the process of somatic hypermutation (loss of peripheral tolerance). The improper exposure of nuclear autoantigens in this delicate location is consequently prone to break self-tolerance to nuclear autoantigens. Indeed, the germline variants of autoantibodies often do not show autoreactivity. The subsequent production of autoantibodies plays a critical role in the development of the complex immunological disorder fostering SLE. Immune complexes composed of cell-derived autoantigens and autoantibodies are formed and get deposited in various tissues, such as the kidney, leading to severe organ damage. Alternatively, they may also be formed in situ by binding to planted antigens of circulating autoantibodies. Here, we review current knowledge about the etiopathogenesis of SLE including the involvement of different types of cell death, serving as the potential source of autoantigens, and impaired clearance of cell remnants, causing accumulation of cellular debris.
免疫系统每天都在对外来抗原做出反应和耐受自身抗原之间艰难平衡,以精细地维持组织内稳态。如果自身耐受性被打破,就可能导致自身免疫性疾病的发生,慢性炎症性自身免疫病系统性红斑狼疮(SLE)就是如此。SLE被认为是一种多因素疾病,涉及多种异常且有害的过程和细胞类型。氧化应激、感染,或者一般而言的组织损伤,都会伴随着大量细胞死亡。诸如凋亡、坏死或NETosis(中性粒细胞胞外陷阱[NETs]的形成)等多种过程可能单独或共同发生。如果对死亡细胞的清除不足,细胞碎片可能会积累,并引发炎症以及细胞质和细胞核自身抗原(如核糖核蛋白、DNA或组蛋白)的泄漏。二级淋巴器官生发中心对细胞残余物清除不充分,可能导致滤泡树突状细胞将自身抗原呈递给在体细胞超突变过程中偶然产生的自身反应性B细胞(外周耐受性丧失)。因此,在这个微妙位置的核自身抗原的不当暴露容易打破对核自身抗原的自身耐受性。事实上,自身抗体的种系变体通常不表现出自反应性。随后自身抗体的产生在促进SLE的复杂免疫紊乱发展中起关键作用。由细胞衍生的自身抗原和自身抗体组成的免疫复合物形成并沉积在各种组织中,如肾脏,导致严重的器官损伤。或者,它们也可能通过与循环自身抗体的植入抗原结合而在原位形成。在这里,我们综述了关于SLE发病机制的当前知识,包括不同类型细胞死亡作为自身抗原的潜在来源的参与情况,以及细胞残余物清除受损导致细胞碎片积累的情况。