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药物性狼疮:传统与新概念。

Drug-induced lupus: Traditional and new concepts.

机构信息

Nephrology Unit, Parma University Hospital, Parma, Italy.

National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD, USA.

出版信息

Autoimmun Rev. 2018 Sep;17(9):912-918. doi: 10.1016/j.autrev.2018.03.016. Epub 2018 Jul 10.

Abstract

Drug-induced lupus (DIL) includes a spectrum of drug-induced reactions often characterised by a clinical phenotype similar to that of idiopathic systemic lupus eruthematosus (SLE) but usually lacking major SLE complications. Different drugs may be associated with distinct clinical and serological profiles, and early recognition is crucial. Drugs traditionally associated with DIL include procainamide, hydralazine, quinidine and others, but strong associations with newer agents, such as TNF α (TNFα) inhibitors, are increasingly recognised. The pathogenic mechanisms explaining how drugs that have heterogeneous chemical structure and function lead to autoimmunity are only partially understood. However, it is likely that traditional DIL-associated agents can boost innate immune responses, particularly neutrophil responses, with neutrophil extracellular trap (NET) formation and exposure of autoantigens. Research in the field of DIL is evolving and may provide interesting models for the study of autoimmunity.

摘要

药物性狼疮(DIL)包括一系列药物诱导的反应,其特征通常为与特发性系统性红斑狼疮(SLE)相似的临床表型,但通常缺乏主要的 SLE 并发症。不同的药物可能与不同的临床和血清学特征相关,早期识别至关重要。传统上与 DIL 相关的药物包括普鲁卡因胺、肼屈嗪、奎尼丁等,但越来越多的证据表明,与新型药物(如 TNFα 抑制剂)也有很强的关联。虽然药物性狼疮的发病机制部分阐明了具有不同化学结构和功能的药物如何导致自身免疫,但很可能是传统的 DIL 相关药物能够增强固有免疫反应,特别是中性粒细胞反应,导致中性粒细胞细胞外陷阱(NET)的形成和自身抗原的暴露。DIL 领域的研究正在不断发展,并可能为自身免疫的研究提供有趣的模型。

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