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Biomarkers for systemic lupus erythematosus: a review and perspective.

机译:系统性红斑狼疮的生物标志物:回顾和观点。

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PURPOSE OF REVIEW: Despite decades of extensive work in the understanding of the etiopathogenesis of systemic lupus erythematosus, few biomarkers have been validated and widely accepted for this disease. The lack of reliable, specific biomarkers not only hampers clinical management of systemic lupus erythematosus but also impedes development of new therapeutic agents. This paper reviews briefly the historical aspects of systemic lupus erythematosus biomarkers and summarizes recent studies on candidate biomarkers. RECENT FINDINGS: Recognizing the urgent need for lupus biomarkers, a Lupus Biomarker Working Group has recently been initiated to facilitate collaborative efforts aimed at identifying and validating biomarkers for systemic lupus erythematosus. Based on available data, several laboratory markers have shown promise as biomarkers for susceptibility, diagnosis, and disease activity. These include Fc receptor genes (disease susceptibility), complement C4d-bound erythrocytes (diagnosis or disease activity), CD27 plasma cells (disease activity), 'interferon signature' (disease activity), and anti-C1q antibodies (disease activity and organ involvement). SUMMARY: There is a longstanding and recently rejuvenated enthusiasm for biomarkers that precisely and specifically reflect the pathophysiologic and clinical changes in systemic lupus erythematosus. Promising candidate biomarkers have been identified but must still be validated through rigorous, large-scale multicenter studies.
机译:审查的目的:尽管数十年来在系统性红斑狼疮的病因发病机理的理解方面进行了广泛的工作,但很少有生物标志物已被验证并被广泛接受。缺乏可靠的,特异性的生物标志物不仅阻碍了系统性红斑狼疮的临床管理,而且阻碍了新治疗剂的开发。本文简要回顾了系统性红斑狼疮生物标志物的历史方面,并总结了有关候选生物标志物的最新研究。最近的发现:认识到对狼疮生物标志物的迫切需求,最近成立了狼疮生物标志物工作组,以促进旨在鉴定和验证系统性红斑狼疮生物标志物的合作努力。根据现有数据,几种实验室标记物已显示出有望用作易感性,诊断和疾病活动的生物标记物。这些包括Fc受体基因(疾病敏感性),与C4d结合的补体红细胞(诊断或疾病活性),CD27浆细胞(疾病活性),“干扰素标记”(疾病活性)和抗C1q抗体(疾病活性和器官受累) )。简介:对于生物标志物存在着长期的热情,并且最近焕发了活力,这些标志物准确而又具体地反映了系统性红斑狼疮的病理生理和临床变化。已经鉴定出有希望的候选生物标志物,但仍必须通过严格的大规模多中心研究进行验证。

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