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自身免疫与自身炎症——是友还是敌?

Autoimmunity versus autoinflammation--friend or foe?

作者信息

Kanazawa Nobuo, Tchernev Georgi, Wollina Uwe

机构信息

Department of Dermatology, Wakayama Medical University, 811-1 Kimiidera, 641-0012, Wakayama, Japan,

出版信息

Wien Med Wochenschr. 2014 Jul;164(13-14):274-7. doi: 10.1007/s10354-014-0290-0. Epub 2014 Jul 9.

Abstract

"Autoimmunity" is a designation dependent on the conventional immunological issue of self/non-self discrimination. Identification of novel target autoantigens is still an important issue ongoing in classical tissue-specific autoimmune bullous diseases and autoimmune connective tissue diseases. In contrast, synchronized with the paradigm shift of the fundamental aspect of immunity to danger sensing/signaling, distinct collagen-like diseases have been defined by the genetic mutations causing dysregulated innate immunity/inflammation and have been designated as “autoinflammatory”diseases. Due to the clinical and etiological similarities,the concept of autoinflammatory diseases has expanded to include non-hereditary collagen-like diseases, tissue-specific chronic idiopathic inflammatory diseases and metabolic diseases. On the other hand, various genetic causes of autoimmune diseases have been identified and the border of these two pathophysiologies is becoming obscure. Instead, a variable mixture of both autoimmunity and autoinflammation can cause each inflammatory phenotype with a variable level of antigen specificity

摘要

“自身免疫”是一个取决于自我/非自我识别这一传统免疫学问题的概念。在经典的组织特异性自身免疫性大疱性疾病和自身免疫性结缔组织疾病中,新型靶自身抗原的鉴定仍是一个重要的研究课题。相比之下,随着免疫基本层面从自我/非自我识别向危险感知/信号传导的范式转变,不同的胶原样疾病已通过导致先天免疫/炎症失调的基因突变得以定义,并被指定为“自身炎症性”疾病。由于临床和病因学上的相似性,自身炎症性疾病的概念已扩展到包括非遗传性胶原样疾病、组织特异性慢性特发性炎症性疾病和代谢性疾病。另一方面,已经确定了自身免疫性疾病的多种遗传病因,这两种病理生理学之间的界限正变得模糊。相反,自身免疫和自身炎症的可变混合可导致具有不同抗原特异性水平的每种炎症表型。

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