Abstract
Therapeutic control of TNFαand IL-1 with specific inhibitors has clearly demonstrated the contribution of these cytokines to the destructive and inflammatory patterns associated with rheumatoid arthritis (RA). At the same time, the list of additional cytokines with similar biological effects has been growing extensively. Among these, IL-17 is of interest since it shares properties and interacts with TNF? and IL-1. In addition, being produced by T cells, demonstration of the contribution of IL-17 in arthritis would add some new information on the contribution of T cells to the pathogenesis of RA. These issues are important since they may lead to new therapeutic applications. Since this topic has been the subject of a recent review, we will focus on the latest developments [1].
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Miossec, P. (2004). IL-17 as a contributor to inflammation and destruction in rheumatoid arthritis. In: van den Berg, W.B., Miossec, P. (eds) Cytokines and Joint Injury. Progress in Inflammation Research. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-7883-8_7
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