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Titlebook: New Therapeutic Targets in Rheumatoid Arthritis; Paul-Peter Tak Book 2009 Birkhäuser Basel 2009 Arthritis.Chemokine.Drug Target.Interleuki

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发表于 2025-3-21 20:01:04 | 显示全部楼层 |阅读模式
书目名称New Therapeutic Targets in Rheumatoid Arthritis
编辑Paul-Peter Tak
视频video
概述Focuses on therapeutic targets that have recently been registered or are currently under development..Each chapter discusses the biological rationale in great detail including results from clinical tr
丛书名称Progress in Inflammation Research
图书封面Titlebook: New Therapeutic Targets in Rheumatoid Arthritis;  Paul-Peter Tak Book 2009 Birkhäuser Basel 2009 Arthritis.Chemokine.Drug Target.Interleuki
描述During the past decades important breakthroughs have been made in the treatment of rheumatoid arthritis (RA). First, the implementation of low-dose methotrexate and other conventional disease-modifying anti-rheumatic drugs was introduced as an effective treatment. Second, it was recognized that early immunomodu- tory treatment is crucial for controlling the disease and its long-term destructive effects more effectively. Parallel advances in research on the pathogenesis of RA and cytokine biology converged in identifying tumor necrosis factor (TNF) as a key factor in inflammation and matrix destruction. The concept arose that elevated TNF concentrations at the sites of inflammation were driving disease pathology, and the removal of excess TNF from sites of inflammation became a therapeutic goal. Clearly, TNF blockade has revolutionized the treatment of RA, as well as other immune-mediated inflammatory diseases. Anti-TNF treatment results in cli- cal benefit in a significant proportion of the patients, and it has provided proof of concept for the principle of targeted therapy. Despite the impressive disease-modifying effects of the TNF blockers, not all patients respond, and patients
出版日期Book 2009
关键词Arthritis; Chemokine; Drug Target; Interleukine; Rheumatology; antibody; cell; clinical trial; diseases; drug
版次1
doihttps://doi.org/10.1007/978-3-7643-8238-4
isbn_ebook978-3-7643-8238-4Series ISSN 1422-7746 Series E-ISSN 2296-4525
issn_series 1422-7746
copyrightBirkhäuser Basel 2009
The information of publication is updating

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Yoshiyuki Ohsugi,Tadamitsu Kishimotoungen PRANDTLS, wenn er im damaligen Institut für Angewandte Mechanik am Leinekanal in Göttingen immer und immer wieder Strömungen im Wassertank beobachtete und dabei häufig genug Ort und Zeit vergaß. Auch war es seine Art, sich von seinen Überlegungen und Rechnungen­ selbst den Zwischenrechnungen - Zeichnung978-3-662-01078-5978-3-662-01077-8
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Co-stimulatory pathways in the therapy of rheumatoid arthritis,on protein combining cytotoxic T lymphocyte antigen 4 (CTLA4) and a portion of the Fc domain of human IgG1, has been approved in the United States and the European Union for the treatment of RA. Abatacept may modulate the T cell or the APC to produce several different outcomes within the joint, incl
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,Immunobiology of IL-6 — Tocilizumab (humanised anti-IL-6 receptor antibody) for the treatment of rh this therapy has also proved quite effective at improving fever, fatigue and anaemia. No serious adverse events have been reported. At present, several international clinical studies of TCZ are ongoing in more than 4000 patients with active RA in 41 countries. The results are continuing to confirm
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Role of IL-18 in inflammatory diseases,ivities and has been shown to be safe in patients. Other options for reducing IL-18 activities are inhibitors of capsase-1, human monoclonal antibodies to IL-18, soluble IL-18 receptors and anti-IL-18 receptor monoclonal antibodies.
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Chemokines and chemokine receptors,ptors. Today, most data in this field are obtained from experimental models of arthritis; however, results of some human trials have also become available. Thus, it is possible that a number of specific chemokine and chemokine receptor antagonists will be administered to arthritis patients in the ne
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Targeting the epigenetic modifications of synovial cells, and infectious agents. So far, these factors have been studied almost exclusively as separate agents. However, gene transcription might be affected by ageing and environmental effects (such as nutrition and infections) — without changes in the nucleotide sequence of the underlying DNA. These patter
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