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Drug-induced autoimmunity.

机译:药物诱导的自身免疫。

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PURPOSE OF REVIEW: This review aims to draw attention to the increased spectrum of the features of drug-induced autoimmunity (DIA), including both clinical and autoantibody profiles in addition to the potential chronicity of the syndrome. RECENT FINDINGS: In recent years, not only has the number of medications causing DIA increased but the spectrum of the features has broadened as well. With the use of newer medications, especially biologics, mostly directed towards immune system manipulation, the range of signs and symptoms of DIA as well as the patterns of autoantibody profiles have widened. Rashes and visceral involvement have started to be reported more often, especially with tumor necrosis factor antagonists. In addition, autoantibodies such as antidouble-stranded DNA, which are usually seen with idiopathic systemic lupus erythematosus, are appearing in place of the antihistone antibodies, typically found in drug-induced lupus. Finally, some medications have been implicated in causing the very same entity, which they may be used to treat. It is clear that progress in the field of pharmacogenetics and pharmacogenomics will help further our understanding of these and other adverse effects of medications. SUMMARY: Even though DIA has been known for many years, the underlying mechanisms remain unclear. However, with recently described new and unexpected features, novel hypotheses have been proposed, thus opening doors to further research in understanding these mechanisms.
机译:综述的目的:这篇综述旨在引起人们对药物诱发的自身免疫(DIA)特征增加的关注,包括该综合征的潜在慢性以及临床和自身抗体特征。最近的发现:近年来,不仅引起DIA的药物数量增加,而且特征范围也扩大了。随着使用更新型药物,尤其是生物制剂,主要针对免疫系统操纵,DIA的体征和症状以及自身抗体谱的模式已扩大。皮疹和内脏受累的报道越来越频繁,尤其是肿瘤坏死因子拮抗剂。另外,通常与特发性系统性红斑狼疮一起出现的自身抗体,例如抗双链DNA,代替了通常在药物诱导的狼疮中发现的抗组蛋白抗体。最后,一些药物可能导致完全相同的实体,可用于治疗。显然,药物遗传学和药物基因组学领域的进展将有助于我们进一步理解药物的这些和其他不良作用。简介:尽管DIA已经知道很多年了,但其潜在机制仍不清楚。然而,随着最近描述的新的和出乎意料的特征,提出了新的假设,从而为进一步研究理解这些机制打开了大门。

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