Anti-TNF biologic agents: still the therapy of choice for rheumatoid arthritis
- PMID: 19798034
- DOI: 10.1038/nrrheum.2009.181
Anti-TNF biologic agents: still the therapy of choice for rheumatoid arthritis
Abstract
Cytokines such as tumor necrosis factor (TNF) are expressed at high levels in rheumatoid joint tissue, where they contribute significantly to inflammation and articular destruction. TNF was the first cytokine to be fully validated as a therapeutic target for rheumatoid arthritis (RA). In nearly a decade since anti-TNF agents-such as infliximab, etanercept and adalimumab-were launched as the first biologic therapies to be licensed for RA, much has been learnt about how and when in the disease course this class of drug can be used to achieve optimal therapeutic benefit. Other cytokine targets, such as interleukin (IL)-6 or IL-1, have also been validated and several are in the process of being tested. However, TNF is likely to remain the preferred target of first-line biologic therapy for the foreseeable future as, in populations with active RA despite ongoing, nonbiologic, DMARD therapy, biologic inhibition of either IL-6 or IL-1 demonstrates no obviously superior outcomes to TNF blockade. Furthermore, new approaches to blockade of signaling mediated by bioactive TNF might have the potential to generate higher-magnitude clinical responses than are currently elicited.
Similar articles
-
[New drugs and treatment strategies for rheumatoid arthritis].Recenti Prog Med. 2003 Sep;94(9):361-79. Recenti Prog Med. 2003. PMID: 12942798 Review. Italian.
-
Emerging biologic drugs for the treatment of rheumatoid arthritis.Autoimmun Rev. 2005 Nov;4(8):537-41. doi: 10.1016/j.autrev.2005.04.016. Autoimmun Rev. 2005. PMID: 16214092 Review.
-
Real-world Effectiveness of Biologic Disease-modifying Antirheumatic Drugs for the Treatment of Rheumatoid Arthritis After Etanercept Discontinuation in the United Kingdom, France, and Germany.Clin Ther. 2017 Aug;39(8):1618-1627. doi: 10.1016/j.clinthera.2017.06.009. Epub 2017 Jul 17. Clin Ther. 2017. PMID: 28729087
-
Cost-effectiveness simulation model of biologic strategies for treating to target rheumatoid arthritis in Germany.Clin Exp Rheumatol. 2013 May-Jun;31(3):400-8. Epub 2013 Mar 4. Clin Exp Rheumatol. 2013. PMID: 23464803
-
Persistence with anti-tumor necrosis factor therapies in patients with rheumatoid arthritis: observations from the RADIUS registry.J Rheumatol. 2011 Jul;38(7):1273-81. doi: 10.3899/jrheum.101142. Epub 2011 May 15. J Rheumatol. 2011. PMID: 21572150
Cited by
-
Treatment with anti-NAP monoclonal antibody reduces disease severity in murine model of novel angiogenic protein-induced or ovalbumin-induced arthritis.Clin Exp Immunol. 2013 Feb;171(2):155-63. doi: 10.1111/cei.12009. Clin Exp Immunol. 2013. PMID: 23286942 Free PMC article.
-
Cell biology: Death by deacetylation.Nature. 2012 Dec 13;492(7428):194-5. doi: 10.1038/nature11761. Epub 2012 Nov 28. Nature. 2012. PMID: 23201692 No abstract available.
-
Evidence for tmTNF reverse signaling in vivo: Implications for an arginase-1-mediated therapeutic effect of TNF inhibitors during inflammation.iScience. 2021 Mar 21;24(4):102331. doi: 10.1016/j.isci.2021.102331. eCollection 2021 Apr 23. iScience. 2021. PMID: 33889824 Free PMC article.
-
A genome-wide association study identifies a new locus associated with the response to anti-TNF therapy in rheumatoid arthritis.Pharmacogenomics J. 2016 Apr;16(2):147-50. doi: 10.1038/tpj.2015.31. Epub 2015 Apr 21. Pharmacogenomics J. 2016. PMID: 25896534
-
Antibodies against ClC7 inhibit extracellular acidification-induced Cl⁻ currents and bone resorption activity in mouse osteoclasts.Naunyn Schmiedebergs Arch Pharmacol. 2011 Jan;383(1):79-90. doi: 10.1007/s00210-010-0576-8. Naunyn Schmiedebergs Arch Pharmacol. 2011. PMID: 21061117
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical