dc.contributor.author
Avci, Ali Berkant
dc.contributor.author
Feist, Eugen
dc.contributor.author
Burmester, Gerd R.
dc.date.accessioned
2025-11-17T15:38:16Z
dc.date.available
2025-11-17T15:38:16Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/50403
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-50129
dc.description.abstract
The use of different pathways in the treatment of rheumatoid arthritis has led to a significant decrease in the number of treatment-resistant patients. In this context, interleukin (IL)-6 inhibition has filled an important gap in rheumatoid arthritis treatment with its effectiveness and safety in both monotherapy and combinations. The process of IL-6 inhibition initiated with IL-6 receptor blockers has prompted questions regarding the potential impact and safety of different inhibitions of this pathway, such as the direct blockade of IL-6. Following the termination of the development of sirukumab because of mortality data in early studies, the investigation of olokizumab, which targets a different region of the IL-6 cytokine, has renewed the hope in this area and the safety concerns have been largely alleviated by the open-label extension data. In addition, the efficacy and safety of tocilizumab and sarilumab have led to a rapid investigation of biosimilars and new potent IL-6 receptor blockers. A comprehensive understanding of mechanisms of this pathway with further long-term clinical data and basic research may provide a decisive impact on selecting the appropriate mechanism as the first choice in personalized treatments.
en
dc.rights.uri
https://creativecommons.org/licenses/by-nc/4.0/
dc.subject
antirheumatic agents
en
dc.subject
Interleukin-6
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Targeting IL-6 or IL-6 Receptor in Rheumatoid Arthritis: What Have We Learned?
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1007/s40259-023-00634-1
dcterms.bibliographicCitation.journaltitle
BioDrugs
dcterms.bibliographicCitation.number
1
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.pagestart
61
dcterms.bibliographicCitation.pageend
71
dcterms.bibliographicCitation.volume
38
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
37989892
dcterms.isPartOf.issn
1173-8804
dcterms.isPartOf.eissn
1179-190X