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在广泛的疾病中通过阻断白细胞介素-1来治疗炎症。

Treating inflammation by blocking interleukin-1 in a broad spectrum of diseases.

机构信息

Department of Medicine, University of Colorado Denver, Aurora, Colorado 80045, USA.

出版信息

Nat Rev Drug Discov. 2012 Aug;11(8):633-52. doi: 10.1038/nrd3800.

DOI:10.1038/nrd3800
PMID:22850787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3644509/
Abstract

Interleukin-1 (IL-1) is a highly active pro-inflammatory cytokine that lowers pain thresholds and damages tissues. Monotherapy blocking IL-1 activity in autoinflammatory syndromes results in a rapid and sustained reduction in disease severity, including reversal of inflammation-mediated loss of sight, hearing and organ function. This approach can therefore be effective in treating common conditions such as post-infarction heart failure, and trials targeting a broad spectrum of new indications are underway. So far, three IL-1-targeted agents have been approved: the IL-1 receptor antagonist anakinra, the soluble decoy receptor rilonacept and the neutralizing monoclonal anti-IL-1β antibody canakinumab. In addition, a monoclonal antibody directed against the IL-1 receptor and a neutralizing anti-IL-1α antibody are in clinical trials.

摘要

白细胞介素-1(IL-1)是一种高度活跃的促炎细胞因子,可降低痛阈并损害组织。在自身炎症性疾病中单药阻断 IL-1 活性可迅速且持续地减轻疾病严重程度,包括逆转炎症介导的视力、听力和器官功能丧失。因此,这种方法可有效治疗常见疾病,如心肌梗死后心力衰竭,针对广泛新适应证的试验正在进行中。迄今为止,已有三种靶向 IL-1 的药物获得批准:白细胞介素-1 受体拮抗剂阿那白滞素、可溶性诱饵受体瑞那司特和中和单克隆抗白细胞介素-1β 抗体卡那单抗。此外,一种针对白细胞介素-1 受体的单克隆抗体和一种中和抗白细胞介素-1α 抗体正在临床试验中。

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