Lundberg Karin, Venables Patrick J
Arthritis Res Ther. 2008;10(6):122. doi: 10.1186/ar2544. Epub 2008 Nov 25.
The paradigm for pathogenic autoimmunity is the generation of high-titre, affinity-matured autoantibodies to a restricted family of autoantigens, in the appropriate genetic context. Genetic determinants of autoimmunity are largely found within the major histocompatibility complex (MHC) and the 'genotype to serotype to phenotype' concept is supported in a number of autoimmune diseases, where both genotype and serotype are well established. The serotype is autoantigen-driven, with evidence of epitope spreading as the disease evolves from asymptomatic to pathogenic autoimmunity. In rheumatoid arthritis and multiple sclerosis, where the autoantigens are poorly characterised, the use of an array in animal models may produce a hint of what happens in human disease. A more complete picture will be obtained from animals transgenic for human MHC, immunised with known human autoantigens.
致病性自身免疫的范例是在适当的遗传背景下,针对有限的自身抗原家族产生高滴度、亲和力成熟的自身抗体。自身免疫的遗传决定因素大多存在于主要组织相容性复合体(MHC)中,并且“基因型-血清型-表型”的概念在许多自身免疫性疾病中得到支持,在这些疾病中,基因型和血清型都已明确确立。血清型由自身抗原驱动,随着疾病从无症状发展为致病性自身免疫,有表位扩展的证据。在类风湿性关节炎和多发性硬化症中,自身抗原的特征尚不明确,在动物模型中使用阵列可能会提示人类疾病中发生的情况。从转人类MHC基因并接种已知人类自身抗原的动物身上将获得更完整的情况。