Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Jun 28;8(7):938.
doi: 10.3390/jcm8070938.

Current Therapeutic Options in the Treatment of Rheumatoid Arthritis

Affiliations
Review

Current Therapeutic Options in the Treatment of Rheumatoid Arthritis

Birgit M Köhler et al. J Clin Med. .

Abstract

Rheumatoid arthritis (RA) is a systemic autoimmune disease characterized by chronic inflammation of the joints. Untreated RA leads to a destruction of joints through the erosion of cartilage and bone. The loss of physical function is the consequence. Early treatment is important to control disease activity and to prevent joint destruction. Nowadays, different classes of drugs with different modes of action are available to control the inflammation and to achieve remission. In this review, we want to discuss differences and similarities of these different drugs.

Keywords: DMARD; MTX; Rheumatoid Arthritis; Tumor Necrosis Factor-Alpha Inhibitors; therapy.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Algorithm adapted from the 2016 European League Against Rheumatism (EULAR) recommendationson rheumatoid arthritis (RA) management. bDMARD, biological; bsDMARD, biosimilar DMARDs; csDMARDs, conventional synthetic DMARDs; DMARDs disease modifying amtirheumatic drug; IL, Interleukin; MTX, methotrexate; TNF, tumor necrosis factor; tsDMARDs, targeted synthetic DMARDS.
Figure 2
Figure 2
Cytokines bind to the receptors, which then undergo a change in their configuration into a dimeric structure, thereby activating their ability to work as a kinase. Consequently, they phosphorylate the STAT molecules (Signal Transducer and Activator of Transcription). Phosphorylated STATs also form dimeres that travel to the cell core, where they activate transcription processes, which further fuel inflammatory processes.

References

    1. Hoes J.N., Jacobs J.W.G., Boers M., Boumpas D., Buttgereit F., Caeyers N., Choy E.H., Cutolo M., Silva J.A.P.D., Esselens G., et al. EULAR evidence-based recommendations on the management of systemic glucocorticoid therapy in rheumatic diseases. Ann. Rheum. Dis. 2007;66:1560–1567. doi: 10.1136/ard.2007.072157. - DOI - PMC - PubMed
    1. Smolen J.S., Landewe R., Breedveld F.C., Buch M., Burmester G., Dougados M., Emery P., Gaujoux-Viala C., Gossec L., Nam J., et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2013 update. Ann. Rheum. Dis. 2014;73:492–509. doi: 10.1136/annrheumdis-2013-204573. - DOI - PMC - PubMed
    1. Smolen J.S., Breedveld F.C., Burmester G.R., Bykerk V., Dougados M., Emery P., Kvien T.K., Navarro-Compan M.V., Oliver S., Schoels M., et al. Treating rheumatoid arthritis to target: 2014 update of the recommendations of an international task force. Ann. Rheum. Dis. 2016;75:3–15. doi: 10.1136/annrheumdis-2015-207524. - DOI - PMC - PubMed
    1. Aletaha D., Smolen J.S. Diagnosis and management of rheumatoid arthritis: A review. JAMA. 2018;320:1360–1372. doi: 10.1001/jama.2018.13103. - DOI - PubMed
    1. Fiehn C., Holle J., Iking-Konert C., Leipe J., Weseloh C., Frerix M., Alten R., Behrens F., Baerwald C., Braun J., et al. S2e guideline: Treatment of rheumatoid arthritis with disease-modifying drugs. Z. Rheumatol. 2018;77:3553. - PubMed

LinkOut - more resources