Mortensen Elin S, Fenton Kristin A, Rekvig Ole P
Department of Pathology, University of Tromsø, N-9037 Tromsø, Norway.
Am J Pathol. 2008 Feb;172(2):275-83. doi: 10.2353/ajpath.2008.070563. Epub 2008 Jan 10.
Systemic lupus erythematosus (SLE) is an autoimmune syndrome characterized by autoantibodies to nuclear constituents. Some of these antibodies are diagnostically important, whereas others act as disease-modifying factors. One clinically important factor is autoantibodies against dsDNA and nucleosomes, which have overlapping diagnostic and nephritogenic impact in SLE. Although a scientific focus for 5 decades, the molecular and cellular origin of these antibodies, and why they are associated with lupus nephritis, is still not fully understood. A consensus has, however, evolved that antibodies to dsDNA and nucleosomes are central pathogenic factors in the development of lupus nephritis. In contrast, no agreement has been reached as to which glomerular structures are bound by nephritogenic anti-nucleosome antibodies in vivo. Mutually contradictory paradigms and models have evolved simply because we still lack precise and conclusive data to provide definitive insight into how autoantibodies induce lupus nephritis and which specificity is critical in the nephritic process(es). In this review, data demonstrating the central role of nucleosomes in inducing and binding potentially nephritogenic antibodies to DNA and nucleosomes are presented and discussed. These autoimmune-inducing processes are discussed in the context of Matzinger's danger model (Matzinger P: Friendly and dangerous signals: is the tissue in control? Nat Immunol 2007, 8:11-13; Matzinger P: The danger model: a renewed sense of self. Science 2002, 296:301-305; Matzinger P: Tolerance, danger, and the extended family. Annu Rev Immunol 1994, 12:991-1045) and Medzhitov's and Janeway's (Medzhitov R, Janeway CA Jr: Decoding the patterns of self and nonself by the innate immune system. Science 2002, 296:298-300; Medzhitov R, Janeway CA Jr: How does the immune system distinguish self from nonself? Semin Immunol 2000, 12:185-188; Janeway CA Jr, Medzhitov R: Innate immune recognition. Annu Rev Immunol 2002, 20:197-216) distinction of noninfectious self (NIS) and infectious nonself (INS). The mechanisms leading to production of potentially nephritogenic anti-nucleosome antibodies and to overt lupus nephritis are interpreted in the context of these paradigms.
系统性红斑狼疮(SLE)是一种自身免疫综合征,其特征是存在针对核成分的自身抗体。其中一些抗体具有诊断意义,而另一些则作为疾病修饰因子起作用。一个临床上重要的因素是抗双链DNA和核小体的自身抗体,它们在SLE中具有重叠的诊断和致肾炎作用。尽管在过去50年里一直是科学研究的重点,但这些抗体的分子和细胞起源以及它们为何与狼疮性肾炎相关,仍未完全明了。然而,目前已形成一种共识,即抗双链DNA和核小体的抗体是狼疮性肾炎发展过程中的核心致病因素。相比之下,关于体内致肾炎性抗核小体抗体结合哪些肾小球结构,尚未达成共识。仅仅因为我们仍然缺乏精确和确凿的数据来深入了解自身抗体如何诱发狼疮性肾炎以及哪种特异性在肾炎过程中至关重要,相互矛盾的范式和模型便应运而生。在这篇综述中,展示并讨论了证明核小体在诱导和结合潜在致肾炎性DNA和核小体抗体方面核心作用的数据。这些自身免疫诱导过程将在Matzinger的危险模型(Matzinger P:友好与危险信号:组织处于控制之中吗?《自然免疫学》2007年,8:11 - 13;Matzinger P:危险模型:对自我的新认识。《科学》2002年,296:301 - 305;Matzinger P:耐受性、危险与大家庭。《免疫学年鉴》1994年,12:991 - 1045)以及Medzhitov和Janeway(Medzhitov R,Janeway CA Jr:通过先天免疫系统解码自我与非自我模式。《科学》2002年,296:298 - 300;Medzhitov R,Janeway CA Jr:免疫系统如何区分自我与非自我?《免疫学期刊》2000年,12:185 - 188;Janeway CA Jr,Medzhitov R:先天免疫识别。《免疫学年鉴》2002年,20:197 - 216)对非感染性自我(NIS)和感染性非自我(INS)的区分背景下进行讨论。导致产生潜在致肾炎性抗核小体抗体并引发明显狼疮性肾炎的机制将在这些范式的背景下进行解读。