Autoantibodies: Focus on anti-DNA antibodies.

Nina Almqvist, Thomas H Winkler, Inga-Lill Mårtensson
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引用次数: 14

Abstract

Ever since the days of Ehrlich and the birth of humoral immunity, self-reactivity or 'horror autotoxicus' as referred to by Paul Ehrlich, has been of great concern. For instance, in patients with the autoimmune disease systemic lupus erythematosus (SLE), anti-nuclear and anti-DNA antibodies have been recognized for many years. Despite this, the exact mechanism as to how the immune system fails to protect the individual and allows these autoantibodies to develop in this and other systemic autoimmune diseases remains uncertain. So how can we explain their presence? Evidence suggests that B cells expressing autoreactive antibodies do not normally arise but rather undergo negative selection as they develop. In light of this, it might seem contradictory that not all autoreactive B cell clones are eliminated, although this may not even be the intention since autoantibodies are also found in healthy individuals and may even protect from autoimmunity. Here, we will discuss autoantibodies, in particular those recognizing DNA, with regard to their reactivity and their potentially pathogenic or protective properties.

自身抗体:专注于抗dna抗体。
自从埃利希的时代和体液免疫的诞生以来,自我反应性或保罗·埃利希所说的“恐怖自体毒性”一直备受关注。例如,在自身免疫性疾病系统性红斑狼疮(SLE)患者中,抗核抗体和抗dna抗体已被发现多年。尽管如此,关于免疫系统如何不能保护个体并允许这些自身抗体在这种和其他系统性自身免疫性疾病中发展的确切机制仍然不确定。那么我们该如何解释它们的存在呢?有证据表明,表达自身反应性抗体的B细胞通常不会出现,而是在发育过程中经历负选择。鉴于此,并不是所有的自身反应性B细胞克隆都被消除,这似乎是矛盾的,尽管这甚至可能不是目的,因为自身抗体也存在于健康个体中,甚至可以保护免受自身免疫。在这里,我们将讨论自身抗体,特别是那些识别DNA的抗体,关于它们的反应性和它们潜在的致病或保护特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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