Anti-TNF-α therapies: the next generation

MA Palladino, FR Bahjat, EA Theodorakis… - Nature reviews Drug …, 2003 - nature.com
MA Palladino, FR Bahjat, EA Theodorakis, LL Moldawer
Nature reviews Drug discovery, 2003nature.com
The functioning of the immune system is finely balanced by the activities of pro-inflammatory
and anti-inflammatory mediators or cytokines. Unregulated activities of these mediators can
lead to the development of serious inflammatory diseases. In particular, enhanced tumour-
necrosis factor-α (TNF-α) synthesis is associated with the development of rheumatoid
arthritis, psoriatic arthritis and inflammatory bowel disease. Inhibiting TNF-α activities in
these diseases has been remarkably successful. However, the current injectable protein …
Abstract
The functioning of the immune system is finely balanced by the activities of pro-inflammatory and anti-inflammatory mediators or cytokines. Unregulated activities of these mediators can lead to the development of serious inflammatory diseases. In particular, enhanced tumour-necrosis factor-α (TNF-α) synthesis is associated with the development of rheumatoid arthritis, psoriatic arthritis and inflammatory bowel disease. Inhibiting TNF-α activities in these diseases has been remarkably successful. However, the current injectable protein therapies have associated risks and limitations. An oral, small molecule that regulates TNF-α biology could either replace the injectables or provide better disease control when used alone or in conjunction with existing therapies. In this review, we discuss briefly the present understanding of TNF-α-mediated biology and the current injectable therapies in clinical use, and focus on some of the new therapeutic approaches with oral, small-molecule inhibitors.
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