Introductory Chapter: Autoantibodies and Their Types

W. Khan
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Abstract

Autoantibodies are groups of antibodies that are directed against body’s own antigen. These autoantibodies are generated against different types of antigens in various autoimmune diseases. Clinical symptoms of systemic autoimmune diseases are characterized by the involvement of various organs in addition to the production of non-organ specific autoantibodies. These autoantibodies in autoimmune diseases are associated with a specific clinical symptom within a spectrum [1]. Most of the autoantibodies have diagnostic and prognostic importance with respect to their associated disease and all of these are not involve in the pathogenesis of these diseases. Most autoantibodies are mainly used as biological markers for certain disease but they do not actually reflect the pathophysiological process underwent during the course of the disease, however, many autoantibodies also have a pathogenetic roles such as antinuclear antibodies and anti-tTG antibodies in celiac disease. For example, autoimmune hepatitis is a chronic disease which is characterized by various clinical, histological as well as immunological characteristics including production of circulating autoantibodies and high serum concentration of gamma globulin [2]. These autoantibodies are very important for the correct diagnosis and classification of autoimmune liver disease [3] and they are not related with the pathogenesis of autoimmune hepatitis. However, some of the systemic autoimmune disease relating these autoantibodies in the sense that their levels are changes during the course of the disease. These include anti-double stranded DNA antibodies in systemic lupus erythematosus (SLE) and anti-neutrophil cytoplasmic autoantibodies in the vasculitis [4]. Other types of antibodies like anti-nucleosome and anti-CIq autoantibodies can function as both markers of the disease activity as well as pathogenic autoantibodies in SLE [5, 6].
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导论章:自身抗体及其类型
自身抗体是一组针对人体自身抗原的抗体。这些自身抗体是针对各种自身免疫性疾病中不同类型的抗原而产生的。全身性自身免疫性疾病的临床症状的特点是除了产生非器官特异性自身抗体外,还累及各种器官。自身免疫性疾病中的这些自身抗体与谱内的特定临床症状相关[1]。大多数自身抗体对其相关疾病具有诊断和预后的重要性,而所有这些抗体都不涉及这些疾病的发病机制。大多数自身抗体主要作为某种疾病的生物学标记物,并不实际反映疾病发生过程中所经历的病理生理过程,但许多自身抗体在乳糜泻中也具有发病作用,如抗核抗体、抗ttg抗体等。例如,自身免疫性肝炎是一种慢性疾病,具有多种临床、组织学和免疫学特征,包括循环自身抗体的产生和血清γ球蛋白的高浓度[2]。这些自身抗体对自身免疫性肝病的正确诊断和分类非常重要[3],与自身免疫性肝炎的发病机制无关。然而,一些系统性自身免疫性疾病与这些自身抗体有关,因为它们的水平在疾病过程中会发生变化。这些抗体包括系统性红斑狼疮(SLE)的抗双链DNA抗体和血管炎的抗中性粒细胞胞浆自身抗体[4]。其他类型的抗体,如抗核小体和抗ciq自身抗体,在SLE中既可以作为疾病活动性的标志物,也可以作为致病性自身抗体[5,6]。
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