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本文引用的文献

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Drugs Today (Barc). 1999 Apr-May;35(4-5):327-51. doi: 10.1358/dot.1999.35.4-5.552208.
2
Chimeric anti-tumor necrosis factor-alpha monoclonal antibody treatment of patients with rheumatoid arthritis receiving methotrexate therapy.接受甲氨蝶呤治疗的类风湿关节炎患者的嵌合抗肿瘤坏死因子-α单克隆抗体治疗。
J Rheumatol. 2000 Apr;27(4):841-50.
3
Anti-cytokine therapy for rheumatoid arthritis.类风湿关节炎的抗细胞因子治疗
Annu Rev Med. 2000;51:207-29. doi: 10.1146/annurev.med.51.1.207.
4
Infliximab (chimeric anti-tumour necrosis factor alpha monoclonal antibody) versus placebo in rheumatoid arthritis patients receiving concomitant methotrexate: a randomised phase III trial. ATTRACT Study Group.英夫利昔单抗(嵌合型抗肿瘤坏死因子α单克隆抗体)与安慰剂用于接受甲氨蝶呤联合治疗的类风湿关节炎患者:一项随机III期试验。ATTRACT研究组。
Lancet. 1999 Dec 4;354(9194):1932-9. doi: 10.1016/s0140-6736(99)05246-0.
5
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J Immunol. 1999 Jul 1;163(1):491-9.
6
Reduction of Th1 cell activity in the peripheral circulation of patients with rheumatoid arthritis after treatment with a non-depleting humanized monoclonal antibody to CD4.
J Rheumatol. 1998 Nov;25(11):2065-76.
7
Immunological treatment of autoimmune diseases.自身免疫性疾病的免疫治疗。
Adv Immunol. 1998;68:333-418. doi: 10.1016/s0065-2776(08)60564-7.
8
Repeat treatment of rheumatoid arthritis patients with a murine anti-intercellular adhesion molecule 1 monoclonal antibody.用鼠抗细胞间黏附分子1单克隆抗体对类风湿关节炎患者进行重复治疗。
Arthritis Rheum. 1997 May;40(5):849-53. doi: 10.1002/art.1780400511.
9
IL-4-induced immune deviation as antigen-specific therapy for inflammatory autoimmune disease.白细胞介素-4诱导的免疫偏离作为炎症性自身免疫病的抗原特异性疗法。
Immunol Today. 1996 May;17(5):225-31. doi: 10.1016/0167-5699(96)80556-1.
10
Manipulation of the Th1/Th2 cell balance: an approach to treat human autoimmune diseases?调节Th1/Th2细胞平衡:一种治疗人类自身免疫性疾病的方法?
Autoimmunity. 1996;23(1):53-68. doi: 10.3109/08916939608995329.

生物疗法将何去何从?

Where is biological therapy going?

作者信息

Schulze-Koops H, Kalden J R

机构信息

Department of Internal Medicine III, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany.

出版信息

Arthritis Res. 2000;2(5):337-41. doi: 10.1186/ar108. Epub 2000 Jun 29.

DOI:10.1186/ar108
PMID:11094444
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC130132/
Abstract

The substantial progress in our understanding of molecular and cellular biology has allowed us to design biological therapeutics ('biologicals') with defined targets and effector functions. These biologicals have greatly contributed to our current knowledge of pathogenetic mechanisms in autoimmune diseases. However, although some of the biologicals have been extremely successful in treating the symptoms of chronic inflammation, biological therapy has not yet met the expectations of permanently silencing the chronic immune response. In this commentary we discuss current concepts and future directions of biological therapy, and the potential usefulness of biologicals as a treatment of human autoimmune diseases in appropriate critical applications with the use of suitably designed agents.

摘要

我们对分子和细胞生物学理解的重大进展使我们能够设计出具有明确靶点和效应功能的生物疗法(“生物制剂”)。这些生物制剂极大地促进了我们目前对自身免疫性疾病发病机制的认识。然而,尽管一些生物制剂在治疗慢性炎症症状方面极其成功,但生物疗法尚未达到永久抑制慢性免疫反应的预期。在这篇评论中,我们讨论了生物疗法的当前概念和未来方向,以及在适当的关键应用中使用精心设计的药物时,生物制剂作为治疗人类自身免疫性疾病的潜在效用。