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抗体工程开发新型抗风湿疗法。

Antibody engineering to develop new antirheumatic therapies.

机构信息

Wilson Horne Immunotherapy Centre and Musculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle-Upon-Tyne NE2 4HH, UK.

出版信息

Arthritis Res Ther. 2009;11(3):225. doi: 10.1186/ar2594. Epub 2009 May 19.

DOI:10.1186/ar2594
PMID:19490600
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2714093/
Abstract

There has been a therapeutic revolution in rheumatology over the past 15 years, characterised by a move away from oral immuno-suppressive drugs toward parenteral targeted biological therapies. The potency and relative safety of the newer agents has facilitated a more aggressive approach to treatment, with many more patients achieving disease remission. There is even a prevailing sense that disease 'cure' may be a realistic goal in the future. These developments were underpinned by an earlier revolution in molecular biology and protein engineering as well as key advances in our understanding of rheumatoid arthritis pathogenesis. This review will focus on antibody engineering as the key driver behind our current and developing range of antirheumatic treatments.

摘要

在过去的 15 年里,风湿病学领域发生了一场治疗革命,其特点是从口服免疫抑制剂转向靶向生物制剂。新型药物的效力和相对安全性促进了更积极的治疗方法,使更多的患者达到疾病缓解。甚至有一种普遍的感觉,即疾病“治愈”可能是未来的一个现实目标。这些发展的基础是分子生物学和蛋白质工程的早期革命,以及对类风湿关节炎发病机制的关键认识的进步。这篇综述将重点介绍抗体工程,因为它是我们当前和正在开发的一系列抗风湿治疗的关键驱动因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/763c/2714093/63dca7e10ed9/ar2594-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/763c/2714093/2ea91dcc45df/ar2594-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/763c/2714093/80a13450f366/ar2594-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/763c/2714093/86568745d9ec/ar2594-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/763c/2714093/63dca7e10ed9/ar2594-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/763c/2714093/2ea91dcc45df/ar2594-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/763c/2714093/80a13450f366/ar2594-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/763c/2714093/86568745d9ec/ar2594-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/763c/2714093/63dca7e10ed9/ar2594-4.jpg

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本文引用的文献

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Golimumab, a human antibody to tumour necrosis factor {alpha} given by monthly subcutaneous injections, in active rheumatoid arthritis despite methotrexate therapy: the GO-FORWARD Study.戈利木单抗,一种通过每月皮下注射给药的抗肿瘤坏死因子α人源抗体,用于尽管接受了甲氨蝶呤治疗但仍处于活动期的类风湿性关节炎:GO-FORWARD研究。
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Certolizumab pegol plus methotrexate is significantly more effective than placebo plus methotrexate in active rheumatoid arthritis: findings of a fifty-two-week, phase III, multicenter, randomized, double-blind, placebo-controlled, parallel-group study.聚乙二醇化赛妥珠单抗联合甲氨蝶呤在活动性类风湿关节炎的治疗中比安慰剂联合甲氨蝶呤显著更有效:一项为期52周的III期多中心随机双盲安慰剂对照平行组研究的结果。
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Flavanoids induce expression of the suppressor of cytokine signalling 3 (SOCS3) gene and suppress IL-6-activated signal transducer and activator of transcription 3 (STAT3) activation in vascular endothelial cells.类黄酮诱导细胞因子信号转导抑制因子 3(SOCS3)基因的表达,并抑制血管内皮细胞中白细胞介素 6 激活的信号转导子和转录激活子 3(STAT3)的激活。
Biochem J. 2013 Sep 1;454(2):283-93. doi: 10.1042/BJ20130481.
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